1. Trang chủ
  2. » Ngoại Ngữ

Atomic force microscopy study of malaria infected red blood cells

196 628 0

Đang tải... (xem toàn văn)

Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống

THÔNG TIN TÀI LIỆU

Thông tin cơ bản

Định dạng
Số trang 196
Dung lượng 19,15 MB

Nội dung

ATOMIC FORCE MICROSCOPY STUDY OF MALARIA INFECTED RED BLOOD CELLS LI ANG NATIONAL UNIVERSITY OF SINGAPORE 2008 ATOMIC FORCE MICROSCOPY STUDY OF MALARIA INFECTED RED BLOOD CELLS LI ANG (B. S., FUDAN UNIVERSITY, CHINA) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARTMENT OF MACHANICAL ENGINEERING NATIONAL UNIVERSITY OF SINGAPORE 2008 Acknowledgements Acknowledgements First of all, I would like to express my utmost gratitude and deepest appreciation to my supervisor, Associate Professor. Lim Chwee Teck for his dedicated support, invaluable insight and guidance, and continuous encouragement in the duration of the study. His influence on me is far beyond this thesis and will benefit me in my future research work. I am much grateful to my co-supervisor, Dr. Tan Shyong Wei, Kevin, for his inspirational help and valuable guidance in my research work. I would also like to thank Dr. Bruce Russel and Associate Professor. Brian Cooke, my outstanding research collaborators, for their constant support, helpful discussion, suggestion, recommendations and valuable perspectives. I really feel fortunate and enjoy working with them. I could not have made it through the four years in NUS without the support and encouragement from my friends, colleagues and current and former members in the Nano Biomechanics Lab. To Ms. Tan Phay Shing, Eunice, Mr. Hairul Nizam Bin Ramli, Ms. Nai Mui Hoon, Brenda, Mr. Lee Yew Yong, Gregory, Dr. Zhou En-Hua, Dr Xu Xiao-Jing for their helpful and friendly guidance during my early time. To Dr. Fu Hong-Xia, Mr. Vedula Sri Ram Krishna, Mr. Lim Tong Seng, Ms. Shi Hui, Ms. Tan Lee Ping, Mr. Chong Ee Jay, Ms. Qie Lan, Mr. Liu Ying, Ms. Ng Sin Yee, Dr. Lee Yew Hoe, Gabriel, Dr. Zhang Ji-Xuan, Ms. Low Yuen Hing, Mr. Li Qing-Sen, Ms. Jiao Gu-Yue, Mr. Tan Swee-Jin, Ms. Yow Soh Zeom, Dr. Zhang You-Sheng, Ms. Sun Wei, Mr. Yuan Jian, Ms. Zhang Rou, I would like to thank i Acknowledgements them for their assistance and contribution in one way or another to the success of this project. Thanks also go to my colleagues in the Laboratory of Molecular and Cellular Parasitology, especially to Ms. Yin Jing, Mr. Ammar Mansoor Hassanbhai, Ms. Ng Geok Choo, Mr. NP Ramachandran, for their assistance and time devoted to the culture of malaria parasite. In addition, I extend my gratitude to Dr. Monica A. Diez Silva, Associate Professor. Usa Lek-Uthai, Dr. Rossarin Suwanarusk, Ms. Kate Fernandez, Dr. John Mills, Professor. Ding Jeak Ling, Associate Professor. Ho Bow, Associate Professor. Sow Chorng Haur, for their helpful academic interactions. I would also like to acknowledge the following people for their friendship: Dr. Zhang Gui-Yong, Ms. Zhang Ying-Yan, Mr. Liu Zhuo, Mr. Li Zi-Rui, Ms. Li Mi, Mr. Luo Rong-Mo, Mr. Huang Liang, Mr. Pan Hai-Ning, Ms. Jiang Hai-Yan, Mr. Zheng Ye. To my family, I appreciate their love, encouragement and support in the duration of this thesis. Especially to my dear wife, Dr. Cheng Yuan, it is impossible for me to finish this work without her support and encouragement. Last but not the least, I am grateful to the National University of Singapore and NUSNNI for granting me the research scholarship which makes my study in NUS possible. Many thanks are conveyed to Department of Mechanical Engineering and Division of Bioengineering, for their material support to every aspect of this work. ii Table of contents Table of Contents ACKNOWLEDGEMENTS I TABLE OF CONTENTS III SUMMARY .VI LIST OF ABBREVIATIONS .VIII LIST OF SYMBOLS . X LIST OF TABLES XI LIST OF FIGURES XII CHAPTER INTRODUCTION . 1.1 Malaria Pathology . 1.1.1 Life Cycle of the Malaria Parasite 1.1.2 Pathogenesis of P. falciparum malaria . 1.2 Current Studies on Surface Morphology and Cytoadherence of IRBCs . 1.2.1 Imaging Techniques for Surface Morphological Studies . 1.2.2 Surface Morphological Studies on the other Plasmodium spp. IRBCs 10 1.2.3 Surface Morphological Studies on Babesia bovis IRBCs . 12 1.2.4 Molecular Mechanism of Cytoadherence of P. falciparum IRBCs 13 1.3 Objective and Scope of This Thesis . 24 1.3.1 Objectives . 24 1.3.2 Scope of Project 25 CHAPTER ATOMIC FORCE MICROSCOPY AND SINGLE-MOLECULE FORCE SPECTROSCOPIC TECHNIQUES 27 2.1 Instrumentation . 28 2.1.1 Working principle . 28 2.1.2 Components 29 2.2 Methods and applications for topographical imaging . 33 iii Table of contents 2.2.1 2.2.2 2.2.3 Operation modes . 33 Sample preparation for cell imaging . 38 Applications in imaging RBC surface 41 2.3 Methods and application in force spectroscopy . 43 2.3.1 Sample preparation . 44 2.3.2 Force mode 46 2.3.3 Interpretation of force curves 50 CHAPTER AFM IMAGING OF SURFACE MORPHOLOGY OF INFECTED CELLS 61 3.1 In-fluid Imaging and Limitations 62 3.1.1 Sample Preparation . 62 3.1.2 Results and Discussion . 64 3.2 Development of a Novel Imaging Method for Simultaneous Monitoring of Surface Morphology and Intracellular Development 68 3.2.1 Sample Preparation . 69 3.2.2 Results and Discussion . 71 3.3 Comparison of Different Laboratory Strains of P. falciparum . 77 3.3.1 Sample Preparation . 77 3.3.2 Results . 78 3.3.3 Discussion . 80 3.4 Changes to the surface of four Plasmodium spp. infected human erythrocytes from clinical isolates . 81 3.4.1 Sample Preparation . 83 3.4.2 Results . 85 3.4.3 Discussion . 95 3.5 Surface Morphology of Babesia-infected Red Cells . 100 3.5.1 Sample Preparation . 102 3.5.2 Results . 104 3.5.3 Discussion . 110 3.6 Conclusions 112 CHAPTER SINGLE MOLECULAR FORCE SPECTROSCOPY STUDY OF LIGAND-RECEPTOR INTERACTIONS INVOLVED IN CYTOADHERENCE . 113 4.1 Methods 114 4.1.1 Sample Preparation: Tip Functionalization 114 iv Table of contents 4.1.2 4.1.3 4.1.4 Sample Preparation: Enrichment of Infected Cells and Substrate Coating 118 AFM Data Collection 122 AFM Data Analysis 123 4.2 Results and Discussion 126 4.2.1 Results . 126 4.2.2 Discussion . 137 4.2.3 Limitations 143 CHAPTER CONCLUSIONS & RECOMMENDATIONS . 145 5.1 Conclusions 145 5.2 Recommendations . 149 PUBLICATIONS ARISING FROM THESIS . 150 REFERENCE 152 v Summary Summary Nano structural changes on the surface of the Plasmodium (P.) spp. infected red blood cells (IRBCs) have a profound importance on the pathobiology of human malaria. Knob-like protrusions have been reported on the surface of P. falciparum and P. malariae IRBCs whereas caveolae are found to be associated with P. vivax and P. ovale IRBCs. In particular, knobs of falciparum IRBCs are the focal adhesion sites mediating the cytoadherence of IRBCs to endothelium aligning the capillary, which is thought to be one of the key mechanisms involved in malaria pathology. However, due to tedious sample preparation and technical limitations associated with previous studies, surface ultrastructural changes of the clinical IRBCs remains unclear. Moreover, as cytoadherence occurs in a highly hydrodynamic environment, the intrinsic kinetic properties of different ligand-receptor interactions are critical in determining their pathological functions, which remain poorly understood. In this thesis, we developed a novel sample preparation protocol for combining Atomic Force Microscopy (AFM) scanning technique and different optical imaging techniques. Here, we comprehensively investigated the surface morphology of different strains as well as different species of human Plasmodium IRBCs and compared that with an animal model, Babesia bovis infection. Significant phenotypic differences between laboratory clones and clinical isolates of P. falciparum infection were found. Inparticular, knobs were not always associated with the surface of infected cells from clinical isolates, and the density of knobs was significantly higher in clinical samples than that in laboratory clones. In addision, distinct surface features of the vi Summary other species of Plasmodium as well as Babesia bovis infected cells were also revealed. A constant number of caveolae was found on the surface of all stages of P. vivax IRBCs whereas P. malariae IRBCs surfaces were covered by numerous ‘knob-like’ structures. The number of ‘ridges’ on the surface of B. bovis IRBCs correlated positively with the strain virulence, suggesting a ‘surface structure’ dependant mechanism determining the severity of the disease. We also applied the single molecular force spectroscopy technique to quantify the dynamic force spectra and characterize the intrinsic kinetic parameters for specific ligand-receptor interactions involved in cytoadherence of P. falciparum infection. Temperature was found to play an important role in affecting the dissociation rates as well as free energy barrier width of different ligands binding to IRBCs. Results from the comparison of CD36 with TSP (both being endothelial receptors that have binding affinities for the malaria exported proteins expressed at the knob) at physiological temperature showed that CD36 mediated interaction was much more stable than that mediated by TSP, although TSP-IRBCs interaction was stronger than CD36-IRBCs interaction in the fast pulling rate regime. This suggests that TSP may initiate the cell adhesion process by catching the fast flowing IRBCs whereas CD36 functions as the major ‘holder’ for providing stable binding. Our study should provide valuable information on the structure-property-function relationship and the biophysical and pathological functions of host receptors and parasite ligands, which will help to identify therapeutic targets and to develop novel drug candidates to reduce the morbidity and mortality burden caused by malaria. vii List of Abbreviations LIST OF ABBREVIATIONS aa AFM ANB-NOS APTES B. BFP BMM BS3 BSA CD36 CIDR CSA CVC EDC EC ECM EM eq. Fc GAGs GPIV GST HA His HOPG HS ICAM-1 LFA-1 Ig IL-1 IMPs IRBCs KAHRP KO. MAC-1 MESA NHS NTA P. amino acid atomic force microscopy N-5-Azido-2-nitrobenzoyloxysuccinimide 3-Aminopropyltriethoxysilane Babesia biomembrane force probe blood media mix Bis(Sulfosuccinimidyl) suberate bovine serum albumin Cell Differentiation antigen 36 cysteine-rich interdomain region chondroitin sulfate A caveolae-vesicle complex 1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide Hydrochloride endothelial cell extracellular matrix electron microscopy equation fragment crystallizable glycosaminoglycans glycoprotein IV glutathione S-transferase hyaluronic acid histidine highly orientated pyrolytic graphite heparan sulfate intercellular adhesion molecule-1 lymphocyte function-associated antigen-1 immunoglobulin interleukin-1 intramembrane particles infected red blood cells knob associated histidine rich proteins knock out Macrophage-1 antigen mature-parasite-infected erythrocyte surface antigen N-hydroxysuccinimide nitrilotriacetic acid Plasmodium viii Reference Gamain, B., Smith, J.D., Miller, L.H., and Baruch, D.I. (2001). Modifications in the CD36 binding domain of the Plasmodium falciparum variant antigen are responsible for the inability of chondroitin sulfate A adherent parasites to bind CD36. Blood 97, 3268-3274. Gamain, B., Smith, J.D., Viebig, N.K., Gysin, J., and Scherf, A. (2007). Pregnancy-associated malaria: parasite binding, natural immunity and vaccine development. Int J Parasitol 37, 273-283. Gao, X.Z., Ye, X.S., and Wang, S.H. (1992). [Ultrastructure of erythrocytic stage of Plasmodium vivax in humans]. Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi 10, 117-119. Garcia, C.R., Takeuschi, M., Yoshioka, K., and Miyamoto, H. (1997). Imaging Plasmodium falciparum-infected ghost and parasite by atomic force microscopy. Journal of structural biology 119, 92-98. Gardiner, D.L., Holt, D.C., Thomas, E.A., Kemp, D.J., and Trenholme, K.R. (2000). Inhibition of Plasmodium falciparum clag9 gene function by antisense RNA. Molecular and biochemical parasitology 110, 33-41. Gearing, A.J., and Newman, W. (1993). Circulating adhesion molecules in disease. Immunol Today 14, 506-512. Girasole, M., Cricenti, A., Generosi, R., Congiu-Castellano, A., Boumis, G., and Amiconi, G. (2001). Artificially induced unusual shape of erythrocytes: an atomic force microscopy study. Journal of microscopy 204, 46-52. Goodyer, I.D., Johnson, J., Eisenthal, R., and Hayes, D.J. (1994). Purification of mature-stage Plasmodium falciparum by gelatine flotation. Ann Trop Med Parasitol 88, 209-211. Gowda, A.S., Madhunapantula, S.V., Achur, R.N., Valiyaveettil, M., Bhavanandan, V.P., and Gowda, D.C. (2007). Structural basis for the adherence of Plasmodium falciparum-infected erythrocytes to chondroitin 4-sulfate and design of novel photoactivable reagents for the identification of parasite adhesive proteins. J Biol Chem 282, 916-928. Grandbois, M., Dettmann, W., Benoit, M., and Gaub, H.E. (2000). Affinity imaging of red blood cells using an atomic force microscope. J Histochem Cytochem 48, 719-724. 161 Reference Greenwalt, D.E., Lipsky, R.H., Ockenhouse, C.F., Ikeda, H., Tandon, N.N., and Jamieson, G.A. (1992). Membrane glycoprotein CD36: a review of its roles in adherence, signal transduction, and transfusion medicine. Blood 80, 1105-1115. Gruenberg, J., Allred, D.R., and Sherman, I.W. (1983). Scanning electron microscope-analysis of the protrusions (knobs) present on the surface of Plasmodium falciparum-infected erythrocytes. J Cell Biol 97, 795-802. Hänggi, P., Talkner, P., and Borkovec, M. (1990). Reaction-rate theory: fifty years after Kramers. Reviews of Modern Physics 62, 251. Hanley, W., McCarty, O., Jadhav, S., Tseng, Y., Wirtz, D., and Konstantopoulos, K. (2003). Single molecule characterization of P-selectin/ligand binding. The Journal of biological chemistry 278, 10556-10561. Hanley, W.D., Wirtz, D., and Konstantopoulos, K. (2004). Distinct kinetic and mechanical properties govern selectin-leukocyte interactions. Journal of cell science 117, 2503-2511. Hasler, T., Handunnetti, S.M., Aguiar, J.C., van Schravendijk, M.R., Greenwood, B.M., Lallinger, G., Cegielski, P., and Howard, R.J. (1990). In vitro rosetting, cytoadherence, and microagglutination properties of Plasmodium falciparum-infected erythrocytes from Gambian and Tanzanian patients. Blood 76, 1845-1852. Hategan, A., Law, R., Kahn, S., and Discher, D.E. (2003). Adhesively-tensed cell membranes: lysis kinetics and atomic force microscopy probing. Biophysical journal 85, 2746-2759. Hermanson, G.T. (1996). Bioconjugate Techniques. Academic Press Hinterdorfer, P. (2002). Molecular recognition studies using the atomic force microscope. Methods Cell Biol 68, 115-139. Hinterdorfer, P., Baumgartner, W., Gruber, H.J., Schilcher, K., and Schindler, H. (1996). Detection and localization of individual antibody-antigen recognition events by atomic force microscopy. Proceedings of the National Academy of Sciences of the United States of America 93, 3477-3481. Ho, M., Schollaardt, T., Niu, X., Looareesuwan, S., Patel, K.D., and Kubes, P. (1998). Characterization of Plasmodium falciparum-infected erythrocyte and P-selectin interaction under flow conditions. Blood 91, 4803-4809. 162 Reference Homer, M.J., Aguilar-Delfin, I., Telford, S.R., 3rd, Krause, P.J., and Persing, D.H. (2000). Babesiosis. Clinical microbiology reviews 13, 451-469. Hutchings, C.L., Li, A., Fernandez, K.M., Fletcher, T., Jackson, L.A., Molloy, J.B., Jorgensen, W.K., Lim, C.T., and Cooke, B.M. (2007). New insights into the altered adhesive and mechanical properties of red blood cells parasitized by Babesia bovis. Mol Microbiol 65, 1092-1105. Hutter, J.L., and Bechhoefer, J. (1993). Calibration of atomic-force microscope tips. Review of Scientific Instruments 64, 1868-1873. Imhof, B.A., and Dunon, D. (1995). Leukocyte migration and adhesion. Adv Immunol 58, 345-416. Jackson, L.A., Waldron, S.J., Weier, H.M., Nicoll, C.L., and Cooke, B.M. (2001). Babesia bovis: culture of laboratory-adapted parasite lines and clinical isolates in a chemically defined medium. Experimental parasitology 99, 168-174. Jacobs, G.H., Aikawa, M., Milhous, W.K., and Rabbege, J.R. (1987). An ultrastructural study of the effects of mefloquine on malaria parasites. Am J Trop Med Hyg 36, 9-14. Janovjak, H., Struckmeier, J., and Muller, D.J. (2005). Hydrodynamic effects in fast AFM single-molecule force measurements. Eur Biophys J 34, 91-96. Janshoff, A., and Steinem, C. (2001). Energy Landscapes of Ligand-Receptor Couples Probed by Dynamic Force Spectroscopy. ChemPhysChem 2, 577-579. Jayavanth, S., Jagadeesan, K., and Singh, M. (2004). Influence of P. vivax malaria on erythrocyte aggregation and deformability. Clin Hemorheol Microcirc 31, 257-266. Karrasch, S., Dolder, M., Schabert, F., Ramsden, J., and Engel, A. (1993). Covalent binding of biological samples to solid supports for scanning probe microscopy in buffer solution. Biophysical journal 65, 2437-2446. Kasas, S., and Ikai, A. (1995). A method for anchoring round shaped cells for atomic force microscope imaging. Biophysical journal 68, 1678-1680. Kersey, F.R., Yount, W.C., and Craig, S.L. (2006). Single-molecule force spectroscopy of bimolecular reactions: system homology in the mechanical activation of ligand substitution reactions. Journal of the American Chemical Society 128, 3886-3887. 163 Reference Klein, D.C., Stroh, C.M., Jensenius, H., van Es, M., Kamruzzahan, A.S., Stamouli, A., Gruber, H.J., Oosterkamp, T.H., and Hinterdorfer, P. (2003). Covalent immobilization of single proteins on mica for molecular recognition force microscopy. Chemphyschem 4, 1367-1371. Korn, C., and Schwarz, U.S. (2006). Efficiency of initiating cell adhesion in hydrodynamic flow. Physical review letters 97, 138103. Kraemer, S.M., and Smith, J.D. (2006). A family affair: var genes, PfEMP1 binding, and malaria disease. Curr Opin Microbiol 9, 374-380. Kramers, H.A. (1940). Brownian motion in a field of force and the diffusion model of chemical reactions. Physica 7, 284-304. Kuhner, F., and Gaub, H.E. (2006). Modelling cantilever-based force spectroscopy with polymers. Polymer 47, 2555-2563. Ladda, R., Aikawa, M., and Sprinz, H. (1969). Penetration of erythrocytes by merozoites of mammalian and avian malarial parasites. J Parasitol 55, 633-644. Lahav, J. (1993). The functions of thrombospondin and its involvement in physiology and pathophysiology. Biochim Biophys Acta 1182, 1-14. Langreth, S.G., Jensen, J.B., Reese, R.T., and Trager, W. (1978a). Fine structure of human malaria in vitro. J Protozool 25, 443-452. Langreth, S.G., Nguyen-Dinh, P., and Trager, W. (1978b). Plasmodium falciparum: merozoite invasion in vitro in the presence of chloroquine. Experimental parasitology 46, 235-238. Lanners, H.N. (1991). Ultrastructure of erythrocytes from Aotus trivirgatus and Saimiri sciureus monkeys infected by Plasmodium vivax. Parasitol Res 77, 395-401. Leech, J.H., Barnwell, J.W., Aikawa, M., Miller, L.H., and Howard, R.J. (1984). Plasmodium falciparum malaria: association of knobs on the surface of infected erythrocytes with a histidine-rich protein and the erythrocyte skeleton. J Cell Biol 98, 1256-1264. Lekka, M., Laidler, P., and Kulik, A.J. (2007). Direct detection of ligand-protein interaction using AFM (Springer). 164 Reference Li, A., Mansoor, A.H., Tan, K.S., and Lim, C.T. (2006). Observations on the internal and surface morphology of malaria infected blood cells using optical and atomic force microscopy. Journal of microbiological methods 66, 434-439. Lim, C.T., Zhou, E.H., Li, A., Vedula, S.R.K., and Fu, H.X. (2005). Experimental techniques for single cell and single molecule biomechanics Materials Science and Engineering: C 26, 1278-1288. Ling, L., Butt, H.J., and Berger, R. (2004). Rupture force between the third strand and the double strand within a triplex DNA. Journal of the American Chemical Society 126, 13992-13997. Liphardt, J., Onoa, B., Smith, S.B., Tinoco, I.J., and Bustamante, C. (2001). Reversible unfolding of single RNA molecules by mechanical force. Science (New York, NY 292, 733-737. Liu, F., Burgess, J., Mizukami, H., and Ostafin, A. (2003). Sample preparation and imaging of erythrocyte cytoskeleton with the atomic force microscopy. Cell Biochemistry and Biophysics 38, 251-270. Liu, F., Mizukami, H., Sarnaik, S., and Ostafin, A. (2005). Calcium-dependent human erythrocyte cytoskeleton stability analysis through atomic force microscopy. Journal of structural biology 150, 200-210. Lo, Y.S., Simons, J., and Beebe, T.P. (2002). Temperature Dependence of the Biotin-Avidin Bond-Rupture Force Studied by Atomic Force Microscopy. Journal of Physical Chemistry B 106, 9847-9852. Lodish, H., Berk, A., Matsudaira, P., Kaiser, C.A., Krieger, M., Scott, M.P., Zipursky, S.L., and Darnell, J.E. (2004). Molecular Cell Biology (W. H. Freeman and Company). Lucas, J.Z., and Sherman, I.W. (1998). Plasmodium falciparum: thrombospondin mediates parasitized erythrocyte band 3-related adhesin binding. Exp Parasitol 89, 78-85. Mackenstedt, U., Brockelman, C.R., Mehlhorn, H., and Raether, W. (1989). Comparative morphology of human and animal malaria parasites. I. Host-parasite interface. Parasitol Res 75, 528-535. MacPherson, G.G., Warrell, M.J., White, N.J., Looareesuwan, S., and Warrell, D.A. (1985). Human cerebral malaria. A quantitative ultrastructural analysis of parasitized erythrocyte sequestration. Am J Pathol 119, 385-401. 165 Reference Maeno, Y., Toyoshima, T., Fujioka, H., Ito, Y., Meshnick, S.R., Benakis, A., Milhous, W.K., and Aikawa, M. (1993). Morphologic effects of artemisinin in Plasmodium falciparum. Am J Trop Med Hyg 49, 485-491. Magowan, C., Wollish, W., Anderson, L., and Leech, J. (1988). Cytoadherence by Plasmodium falciparum-infected erythrocytes is correlated with the expression of a family of variable proteins on infected erythrocytes. J Exp Med 168, 1307-1320. Mangold, K.A., Manson, R.U., Koay, E.S., Stephens, L., Regner, M., Thomson, R.B., Jr., Peterson, L.R., and Kaul, K.L. (2005). Real-time PCR for detection and identification of Plasmodium spp. J Clin Microbiol 43, 2435-2440. Marshall, B.T., Long, M., Piper, J.W., Yago, T., McEver, R.P., and Zhu, C. (2003). Direct observation of catch bonds involving cell-adhesion molecules. Nature 423, 190-193. Maruyama, I., Bell, C.E., and Majerus, P.W. (1985). Thrombomodulin is found on endothelium of arteries, veins, capillaries, and lymphatics, and on syncytiotrophoblast of human placenta. J Cell Biol 101, 363-371. Matsumoto, Y., Matsuda, S., and Yoshida, Y. (1986). Ultrastructure of human erythrocytes infected with Plasmodium ovale. Am J Trop Med Hyg 35, 697-703. Matzke, R., Jacobson, K., and Radmacher, M. (2001). Direct, high-resolution measurement of furrow stiffening during division of adherent cells. Nat Cell Biol 3, 607-610. Maubert, B., Guilbert, L.J., and Deloron, P. (1997). Cytoadherence of Plasmodium falciparum to intercellular adhesion molecule and chondroitin-4-sulfate expressed by the syncytiotrophoblast in the human placenta. Infect Immun 65, 1251-1257. McCormick, C.J., Craig, A., Roberts, D., Newbold, C.I., and Berendt, A.R. (1997). Intercellular adhesion molecule-1 and CD36 synergize to mediate adherence of Plasmodium falciparum-infected erythrocytes to cultured human microvascular endothelial cells. J Clin Invest 100, 2521-2529. Meadows, P.Y., Bemis, J.E., and Walker, G.C. (2005). Quantifying adhesion bond parameters to distinguish interactions of hydrophilic and hydrophobic blocks of polystyrene-poly-2-vinylpyridine with a silicon nitride surface. Journal of the American Chemical Society 127, 4136-4137. 166 Reference Merkel, R., Nassoy, P., Leung, A., Ritchie, K., and Evans, E. (1999a). Energy landscapes of receptor-ligand bonds explored with dynamic force spectroscopy. Nature 397, 50-53. Merkel, R., Nassoy, P., Leung, A., Ritchie, K., and Evans, E. (1999b). Energy landscapes of receptor-ligand bonds explored with dynamic force spectroscopy. Nature 397, 50-53. Miller, L.H. (1969). Distribution of mature trophozoites and schizonts of Plasmodium falciparum in the organs of Aotus trivirgatus, the night monkey. Am J Trop Med Hyg 18, 860-865. Miller, L.H., Baruch, D.I., Marsh, K., and Doumbo, O.K. (2002). The pathogenic basis of malaria. Nature 415, 673-679. Milne, L.M., Kyi, M.S., Chiodini, P.L., and Warhurst, D.C. (1994). Accuracy of routine laboratory diagnosis of malaria in the United Kingdom. J Clin Pathol 47, 740-742. Mohapatra, M.K., Padhiary, K.N., Mishra, D.P., and Sethy, G. (2002). Atypical manifestations of Plasmodium vivax malaria. Indian J Malariol 39, 18-25. Montgomery, J., Mphande, F.A., Berriman, M., Pain, A., Rogerson, S.J., Taylor, T.E., Molyneux, M.E., and Craig, A. (2007). Differential var gene expression in the organs of patients dying of falciparum malaria. Mol Microbiol. Nagao, E., Kaneko, O., and Dvorak, J.A. (2000a). Plasmodium falciparum-infected erythrocytes: qualitative and quantitative analyses of parasite-induced knobs by atomic force microscopy. J Struct Biol 130, 34-44. Nagao, E., Nishijima, H., Akita, S., Nakayama, Y., and Dvorak, J.A. (2000b). The cell biological application of carbon nanotube probes for atomic force microscopy: comparative studies of malaria-infected erythrocytes. Journal of electron microscopy 49, 453-458. Nakamura, K., Hasler, T., Morehead, K., Howard, R.J., and Aikawa, M. (1992). Plasmodium falciparum-infected erythrocyte receptor(s) for CD36 and thrombospondin are restricted to knobs on the erythrocyte surface. J Histochem Cytochem 40, 1419-1422. Nevo, R., Brumfeld, V., Kapon, R., Hinterdorfer, P., and Reich, Z. (2005). Direct measurement of protein energy landscape roughness. EMBO reports 6, 482-486. 167 Reference Newbold, C., Craig, A., Kyes, S., Rowe, A., Fernandez-Reyes, D., and Fagan, T. (1999). Cytoadherence, pathogenesis and the infected red cell surface in Plasmodium falciparum. Int J Parasitol 29, 927-937. Newbold, C., Warn, P., Black, G., Berendt, A., Craig, A., Snow, B., Msobo, M., Peshu, N., and Marsh, K. (1997). Receptor-specific adhesion and clinical disease in Plasmodium falciparum. The American journal of tropical medicine and hygiene 57, 389-398. Nowakowski, R., Luckham, P., and Winlove, P. (2001). Imaging erythrocytes under physiological conditions by atomic force microscopy. Biochimica et biophysica acta 1514, 170-176. O'Connor, R.M., Long, J.A., and Allred, D.R. (1999). Cytoadherence of Babesia bovis-infected erythrocytes to bovine brain capillary endothelial cells provides an in vitro model for sequestration. Infect Immun 67, 3921-3928. O'Reilly, M., McDonnell, L., and O'Mullane, J. (2001). Quantification of red blood cells using atomic force microscopy. Ultramicroscopy 86, 107-112. Oakley, M.S.M., Kumar, S., Anantharaman, V., Zheng, H., Mahajan, B., Haynes, J.D., Moch, J.K., Fairhurst, R., McCutchan, T.F., and Aravind, L. (2007). Molecular Factors and Biochemical Pathways Induced by Febrile Temperature in Intraerythrocytic Plasmodium falciparum Parasites. Infection and immunity 75, 2012-2025. Ockenhouse, C.F., Ho, M., Tandon, N.N., Van Seventer, G.A., Shaw, S., White, N.J., Jamieson, G.A., Chulay, J.D., and Webster, H.K. (1991a). Molecular basis of sequestration in severe and uncomplicated Plasmodium falciparum malaria: differential adhesion of infected erythrocytes to CD36 and ICAM-1. J Infect Dis 164, 163-169. Ockenhouse, C.F., Klotz, F.W., Tandon, N.N., and Jamieson, G.A. (1991b). Sequestrin, a CD36 recognition protein on Plasmodium falciparum malaria-infected erythrocytes identified by anti-idiotype antibodies. Proceedings of the National Academy of Sciences of the United States of America 88, 3175-3179. Ockenhouse, C.F., Tandon, N.N., Magowan, C., Jamieson, G.A., and Chulay, J.D. (1989). Identification of a platelet membrane glycoprotein as a falciparum malaria sequestration receptor. Science 243, 1469-1471. Ockenhouse, C.F., Tegoshi, T., Maeno, Y., Benjamin, C., Ho, M., Kan, K.E., Thway, Y., Win, K., Aikawa, M., and Lobb, R.R. (1992). Human vascular endothelial cell adhesion receptors for Plasmodium falciparum-infected erythrocytes: roles for 168 Reference endothelial leukocyte adhesion molecule and vascular cell adhesion molecule 1. J Exp Med 176, 1183-1189. Oh, S.S., Voigt, S., Fisher, D., Yi, S.J., LeRoy, P.J., Derick, L.H., Liu, S., and Chishti, A.H. (2000). Plasmodium falciparum erythrocyte membrane protein is anchored to the actin-spectrin junction and knob-associated histidine-rich protein in the erythrocyte skeleton. Mol Biochem Parasitol 108, 237-247. Oo, M.M., Aikawa, M., Than, T., Aye, T.M., Myint, P.T., Igarashi, I., and Schoene, W.C. (1987). Human cerebral malaria: a pathological study. J Neuropathol Exp Neurol 46, 223-231. Oquendo, P., Hundt, E., Lawler, J., and Seed, B. (1989). CD36 directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes. Cell 58, 95-101. Ozen, M., Gungor, S., Atambay, M., and Daldal, N. (2006). Cerebral malaria owing to Plasmodium vivax: case report. Ann Trop Paediatr 26, 141-144. Padley, D., Moody, A.H., Chiodini, P.L., and Saldanha, J. (2003). Use of a rapid, single-round, multiplex PCR to detect malarial parasites and identify the species present. Ann Trop Med Parasitol 97, 131-137. Panorchan, P., Thompson, M.S., Davis, K.J., Tseng, Y., Konstantopoulos, K., and Wirtz, D. (2006). Single-molecule analysis of cadherin-mediated cell-cell adhesion. Journal of cell science 119, 66-74. Perret, E., Leung, A., Feracci, H., and Evans, E. (2004). Trans-bonded pairs of E-cadherin exhibit a remarkable hierarchy of mechanical strengths. Proceedings of the National Academy of Sciences of the United States of America 101, 16472-16477. Pongponratn, E., Turner, G.D., Day, N.P., Phu, N.H., Simpson, J.A., Stepniewska, K., Mai, N.T., Viriyavejakul, P., Looareesuwan, S., Hien, T.T., et al. (2003). An ultrastructural study of the brain in fatal Plasmodium falciparum malaria. The American journal of tropical medicine and hygiene 69, 345-359. Pouvelle, B., Spiegel, R., Hsiao, L., Howard, R.J., Morris, R.L., Thomas, A.P., and Taraschi, T.F. (1991). Direct access to serum macromolecules by intraerythrocytic malaria parasites. Nature 353, 73-75. Prudhomme, J.G., Sherman, I.W., Land, K.M., Moses, A.V., Stenglein, S., and Nelson, J.A. (1996). Studies of Plasmodium falciparum cytoadherence using immortalized human brain capillary endothelial cells. Int J Parasitol 26, 647-655. 169 Reference Putman, C.A.J., De Grooth, B.G., Van Hulst, N.F., and Greve, J. (1992). A detailed analysis of the optical beam deflection technique for use in atomic force microscopy. Journal of Applied Physics 72, 6-12. Raventos-Suarez, C., Kaul, D.K., Macaluso, F., and Nagel, R.L. (1985). Membrane knobs are required for the microcirculatory obstruction induced by Plasmodium falciparum-infected erythrocytes. Proc Natl Acad Sci U S A 82, 3829-3833. Ray, C., and Akhremitchev, B.B. (2005). Conformational heterogeneity of surface-grafted amyloidogenic fragments of alpha-synuclein dimers detected by atomic force microscopy. Journal of the American Chemical Society 127, 14739-14744. Ray, C., Brown, J.R., and Akhremitchev, B.B. (2007). Rupture force analysis and the associated systematic errors in force spectroscopy by AFM. Langmuir 23, 6076-6083. Roberts, D.D., Sherwood, J.A., Spitalnik, S.L., Panton, L.J., Howard, R.J., Dixit, V.M., Frazier, W.A., Miller, L.H., and Ginsburg, V. (1985). Thrombospondin binds falciparum malaria parasitized erythrocytes and may mediate cytoadherence. Nature 318, 64-66. Roberts, D.J., Craig, A.G., Berendt, A.R., Pinches, R., Nash, G., Marsh, K., and Newbold, C.I. (1992). Rapid switching to multiple antigenic and adhesive phenotypes in malaria. Nature 357, 689-692. Rock, E.P., Roth, E.F., Jr., Rojas-Corona, R.R., Sherwood, J.A., Nagel, R.L., Howard, R.J., and Kaul, D.K. (1988). Thrombospondin mediates the cytoadherence of Plasmodium falciparum-infected red cells to vascular endothelium in shear flow conditions. Blood 71, 71-75. Rogerson, S.J., Chaiyaroj, S.C., Ng, K., Reeder, J.C., and Brown, G.V. (1995). Chondroitin sulfate A is a cell surface receptor for Plasmodium falciparum-infected erythrocytes. J Exp Med 182, 15-20. Rotsch, C., Braet, F., Wisse, E., and Radmacher, M. (1997). AFM imaging and elasticity measurements on living rat liver macrophages. Cell Biol Int 21, 685-696. Ruangjirachuporn, W., Afzelius, B.A., Helmby, H., Hill, A.V., Greenwood, B.M., Carlson, J., Berzins, K., Perlmann, P., and Wahlgren, M. (1992). Ultrastructural analysis of fresh Plasmodium falciparum-infected erythrocytes and their cytoadherence to human leukocytes. The American journal of tropical medicine and hygiene 46, 511-519. 170 Reference Rug, M., Prescott, S.W., Fernandez, K.M., Cooke, B.M., and Cowman, A.F. (2006). The role of KAHRP domains in knob formation and cytoadherence of P falciparum-infected human erythrocytes. Blood 108, 370-378. Sader, J.E. (1995). Parallel beam approximation for V-shaped atomic force microscope cantilevers. Review of Scientific Instruments 66, 4583-4587. Sader, J.E., Larson, I., Mulvaney, P., and White, L.R. (1995). Method for the calibration of atomic force microscope cantilevers. Review of Scientific Instruments 66, 3789-3798. Sader, J.E., and White, L. (1993). Theoretical analysis of the static deflection of plates for atomic force microscope applications. Journal of Applied Physics 74, 1-9. Scheffer, L., Bitler, A., Ben-Jacob, E., and Korenstein, R. (2001). Atomic force pulling: probing the local elasticity of the cell membrane. Eur Biophys J 30, 83-90. Schetters, T.P., and Eling, W.M. (1999). Can Babesia infections be used as a model for cerebral malaria? Parasitology today (Personal ed 15, 492-497. Senden, T., and Ducker, W. (1994). Experimental Determination of Spring Constants in Atomic Force Microscopy. Langmuir 10, 1003-1004. Serghides, L., Crandall, I., Hull, E., and Kain, K.C. (1998). The Plasmodium falciparum-CD36 interaction is modified by a single amino acid substitution in CD36. Blood 92, 1814-1819. Serghides, L., Smith, T.G., Patel, S.N., and Kain, K.C. (2003). CD36 and malaria: friends or foes? Trends in parasitology 19, 461-469. Shao, Z., Mou, J., Czajkowsky, D.M., Yang, J., and Yuan, J.-Y. (1996). Biological atomic force microscopy: what is achieved and what is needed. Advances in Physics 45, 1-86. Sherman, I.W., Eda, S., and Winograd, E. (2003). Cytoadherence and sequestration in Plasmodium falciparum: defining the ties that bind. Microbes Infect 5, 897-909. Sherwood, J.A., Roberts, D.D., Marsh, K., Harvey, E.B., Spitalnik, S.L., Miller, L.H., and Howard, R.J. (1987). Thrombospondin binding by parasitized erythrocyte isolates in falciparum malaria. Am J Trop Med Hyg 36, 228-233. Siano, J.P., Grady, K.K., Millet, P., Swerlick, R.A., and Wick, T.M. (1997). Plasmodium falciparum: soluble thrombospondin increases cytoadherence of 171 Reference parasitized erythrocytes to human microvascular endothelium under shear flow conditions. Exp Parasitol 87, 69-72. Siano, J.P., Grady, K.K., Millet, P., and Wick, T.M. (1998). Short report: Plasmodium falciparum: cytoadherence to alpha(v)beta3 on human microvascular endothelial cells. Am J Trop Med Hyg 59, 77-79. Smith, D.H., and Theakston, R.D. (1970). Comments on the ultrastructure of human erythrocytes infected with Plasmodium malariae. Annals of tropical medicine and parasitology 64, 329. Snow, R.W., Guerra, C.A., Noor, A.M., Myint, H.Y., and Hay, S.I. (2005). The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature 434, 214-217. Staunton, D.E., Dustin, M.L., Erickson, H.P., and Springer, T.A. (1990). The arrangement of the immunoglobulin-like domains of ICAM-1 and the binding sites for LFA-1 and rhinovirus. Cell 61, 243-254. Stroh, C., Wang, H., Bash, R., Ashcroft, B., Nelson, J., Gruber, H., Lohr, D., Lindsay, S.M., and Hinterdorfer, P. (2004). Single-molecule recognition imaging microscopy. Proceedings of the National Academy of Sciences of the United States of America 101, 12503-12507. Su, X.Z., Heatwole, V.M., Wertheimer, S.P., Guinet, F., Herrfeldt, J.A., Peterson, D.S., Ravetch, J.A., and Wellems, T.E. (1995). The large diverse gene family var encodes proteins involved in cytoadherence and antigenic variation of Plasmodium falciparum-infected erythrocytes. Cell 82, 89-100. Sulchek, T.A., Friddle, R.W., Langry, K., Lau, E.Y., Albrecht, H., Ratto, T.V., DeNardo, S.J., Colvin, M.E., and Noy, A. (2005). Dynamic force spectroscopy of parallel individual Mucin1-antibody bonds. Proceedings of the National Academy of Sciences of the United States of America 102, 16638-16643. Suwanarusk, R., Cooke, B.M., Dondorp, A.M., Silamut, K., Sattabongkot, J., White, N.J., and Udomsangpetch, R. (2004). The deformability of red blood cells parasitized by Plasmodium falciparum and P. vivax. J Infect Dis 189, 190-194. Swihart, A.H., Mikrut, J.M., Ketterson, J.B., and Macdonald, R.C. (2001). Atomic force microscopy of the erythrocyte membrane skeleton. Journal of microscopy 204, 212-225. 172 Reference Taylor, M.E. (1993). Dynamics of piezoelectric tube scanners for scanning probe microscopy. Review of Scientific Instruments 64, 154-158. Tees, D.F., Waugh, R.E., and Hammer, D.A. (2001). A microcantilever device to assess the effect of force on the lifetime of selectin-carbohydrate bonds. Biophysical journal 80, 668-682. Touhami, A., Jericho, M.H., and Beveridge, T.J. (2004). Atomic force microscopy of cell growth and division in Staphylococcus aureus. Journal of bacteriology 186, 3286-3295. Trager, W. (1989). Erythrocyte knobs and malaria. Nature 340, 352. Trager, W., and Jensen, J.B. (1976). Human malaria parasites in continuous culture. Science (New York, NY 193, 673-675. Trager, W., Rudzinska, M.A., and Bradbury, P.C. (1966). The fine structure of Plasmodium falciparum and its host erythrocytes in natural malarial infections in man. Bull World Health Organ 35, 883-885. Trang, D.T., Huy, N.T., Kariu, T., Tajima, K., and Kamei, K. (2004). One-step concentration of malarial parasite-infected red blood cells and removal of contaminating white blood cells. Malar J 3, 7. Trenholme, K.R., Gardiner, D.L., Holt, D.C., Thomas, E.A., Cowman, A.F., and Kemp, D.J. (2000). clag9: A cytoadherence gene in Plasmodium falciparum essential for binding of parasitized erythrocytes to CD36. Proc Natl Acad Sci U S A 97, 4029-4033. Treutiger, C.J., Heddini, A., Fernandez, V., Muller, W.A., and Wahlgren, M. (1997). PECAM-1/CD31, an endothelial receptor for binding Plasmodium falciparum-infected erythrocytes. Nat Med 3, 1405-1408. Tuvia, S., Almagor, A., Bitler, A., Levin, S., Korenstein, R., and Yedgar, S. (1997). Cell membrane fluctuations are regulated by medium macroviscosity: evidence for a metabolic driving force. Proceedings of the National Academy of Sciences of the United States of America 94, 5045-5049. Udagama, P.V., Atkinson, C.T., Peiris, J.S., David, P.H., Mendis, K.N., and Aikawa, M. (1988). Immunoelectron microscopy of Schuffner's dots in Plasmodium vivax-infected human erythrocytes. Am J Pathol 131, 48-52. 173 Reference Udomsangpetch, R., Aikawa, M., Berzins, K., Wahlgren, M., and Perlmann, P. (1989). Cytoadherence of knobless Plasmodium falciparum-infected erythrocytes and its inhibition by a human monoclonal antibody. Nature 338, 763-765. Udomsangpetch, R., Pipitaporn, B., Silamut, K., Pinches, R., Kyes, S., Looareesuwan, S., Newbold, C., and White, N.J. (2002). Febrile temperatures induce cytoadherence of ring-stage Plasmodium falciparum-infected erythrocytes. Proceedings of the National Academy of Sciences 99, 11825-11829. Verbelen, C., Dupres, V., Menozzi, F.D., Raze, D., Baulard, A.R., Hols, P., and Dufrene, Y.F. (2006). Ethambutol-induced alterations in Mycobacterium bovis BCG imaged by atomic force microscopy. FEMS microbiology letters 264, 192-197. Vinetz, J.M., Li, J., McCutchan, T.F., and Kaslow, D.C. (1998). Plasmodium malariae infection in an asymptomatic 74-year-old Greek woman with splenomegaly. N Engl J Med 338, 367-371. Voigt, S., Hanspal, M., LeRoy, P.J., Zhao, P.S., Oh, S.S., Chishti, A.H., and Liu, S.C. (2000). The cytoadherence ligand Plasmodium falciparum erythrocyte membrane protein (PfEMP1) binds to the P. falciparum knob-associated histidine-rich protein (KAHRP) by electrostatic interactions. Mol Biochem Parasitol 110, 423-428. Waller, K.L., Cooke, B.M., Nunomura, W., Mohandas, N., and Coppel, R.L. (1999). Mapping the binding domains involved in the interaction between the Plasmodium falciparum knob-associated histidine-rich protein (KAHRP) and the cytoadherence ligand P. falciparum erythrocyte membrane protein (PfEMP1). J Biol Chem 274, 23808-23813. Waterkeyn, J.G., Cowman, A.F., and Cooke, B.M. (2001). Plasmodium falciparum: gelatin enrichment selects for parasites with full-length chromosome 2. implications for cytoadhesion assays. Experimental parasitology 97, 115-118. Waterkeyn, J.G., Wickham, M.E., Davern, K.M., Cooke, B.M., Coppel, R.L., Reeder, J.C., Culvenor, J.G., Waller, R.F., and Cowman, A.F. (2000). Targeted mutagenesis of Plasmodium falciparum erythrocyte membrane protein (PfEMP3) disrupts cytoadherence of malaria-infected red blood cells. The EMBO journal 19, 2813-2823. WHO (2005). World Malaria Report 2005. Wolf, H., and Gingell, D. (1983). Conformational response of the glycocalyx to ionic strength and interaction with modified glass surfaces: study of live red cells by interferometry. Journal of cell science 63, 101-112. 174 Reference Wright, I.G. (1972). An electron microscopic study of intravascular agglutination in the cerebral cortex due to Babesia argentina infection. Int J Parasitol 2, 209-215. Wright, I.G., Goodger, B.M., McKenna, R.V., and Mahoney, D.F. (1979). Acute Babesia bovis infection: a study of the vascular leisons in kidney and lung. Z parasitenkd 60, 19-27. Wright, I.G., and Goodger, B.V. (1979). Acute Babesia bovis infections: renal involvement in the hypotensive syndrome. Zeitschrift fur Parasitenkunde (Berlin, Germany) 59, 115-119. Wright, I.G., Goodger, B.V., and Clark, I.A. (1988). Immunopathophysiology of Babesia bovis and Plasmodium falciparum infections. Parasitology today (Personal ed 4, 214-218. Yago, T., Wu, J., Wey, C.D., Klopocki, A.G., Zhu, C., and McEver, R.P. (2004). Catch bonds govern adhesion through L-selectin at threshold shear. The Journal of Cell Biology 166, 913-923. Yipp, B.G., Hickey, M.J., Andonegui, G., Murray, A.G., Looareesuwan, S., Kubes, P., and Ho, M. (2007). Differential roles of CD36, ICAM-1, and P-selectin in Plasmodium falciparum cytoadherence in vivo. Microcirculation 14, 593-602. Yuan, C., Chen, A., Kolb, P., and Moy, V.T. (2000). Energy landscape of streptavidin-biotin complexes measured by atomic force microscopy. Biochemistry 39, 10219-10223. Zachee, P., Boogaerts, M., Snauwaert, J., and Hellemans, L. (1994). Imaging uremic red blood cells with the atomic force microscope. American journal of nephrology 14, 197-200. Zachee, P., Boogaerts, M.A., Hellamans, L., and Snauwaert, J. (1992). Adverse role of the spleen in hereditary spherocytosis: evidence by the use of the atomic force microscope. British journal of haematology 80, 264-265. Zhang, P.C., Bai, C., Huang, Y.M., Zhao, H., Fang, Y., Wang, N.X., and Li, Q. (1995). Atomic force microscopy study of fine structures of the entire surface of red blood cells. Scanning microscopy 9, 981-989; discussion 1009-1010. Zhong, Q., Inniss, D., Kjoller, K., and Elings, V.B. (1993). Fractured polymer/silica fiber surface studied by tapping mode atomic force microscopy. Surface Science Letters 290, 688-692. 175 Reference Zou, S., Schonherr, H., and Vancso, G.J. (2005). Force spectroscopy of quadruple H-bonded dimers by AFM: dynamic bond rupture and molecular time-temperature superposition. Journal of the American Chemical Society 127, 11230-11231. 176 [...]... constitute less than 2% of the total blood volume Whereas P malariae only infects older red cells with the number even more limited 2 The unique sequestration or cytoadherence property of P falciparum infected red cells may cause ‘mechanical’ vascular obstructions It has been observed for over a century (Bignami and Bastianelli, 1889) that only early ring stage falciparum infected red cells appear in peripheral... (account for 95% of total infection) and P falciparum being responsible for more than 90% of malaria related deaths The following sections of this chapter will discuss the general aspects of malaria parasite biology with a focus on P falciparum 1.1.1 Life Cycle of the Malaria Parasite The life cycle of the malaria parasite is shown in Figure 1.1 Infection in humans is initiated when an infected Anopheles... the number of ridges on the surface of B bovis -infected RBCs in relation to parasite maturity and level of virulence Typical AFM images showing the variation in the number of ridges present on the surface of bovine RBCs infected with either single (B and D) or paired (A and C) forms of B bovis (Anderson or K-strain) 107 Figure 3.20 Statistical quantification of density (A) and height (B) of ridges... scanning electron microscopy (SEM), which provides more detailed surface images of the sample than TEM A comprehensive study on the surface morphology of falciparum IRBCs was performed by Gruenberg et al in 1983 (Gruenberg et al., 1983) They compared the SEM images of different stages of infected cells and found the number and density of knob structures changed This is the first study focusing on quantitative... morphology of B bovis of different strains at different stages still remains unclear 1.2.4 Molecular Mechanism of Cytoadherence of P falciparum IRBCs Direct evidence of cytoadherence originates from histological examinations of the microcirculation in blood vessels from cerebral malaria patients in which large amounts of late stage parasitized cells accumulate and sequentially perturb or fully obstruct the blood. .. Parasite invasion of red blood cells (RBCs) involves specific interactions between merozoite surface antigens and erythrocyte membrane proteins and unfolds in four steps: initial contact; reorientation and junction formation; deformation of host cell membrane and entry of merozoite; and resealing of erythrocyte membrane (Aikawa et al., 1978; Dvorak et al., 1975) Once within the host red blood cells, the merozoites... knobby microgametocyte of P malariae (B) 94 Figure 3.18 Surface architecture of PRBCs imaged by atomic force microscopy (Hutchings et al., 2007) (A) Bovine RBC infected with B bovis showing ridge protrusions visible on the cell surface (B) Higher magnification of the RBC in (A) showing ridge morphology in greater detail (C) Bovine RBC infected with B bigemina Note the absence of ridges on the RBC... have been observed over the surface of malaria infected RBCs: the ‘knobs’ of P falciparum and P malariae (some evidence suggests their presence on P ovlae) and ‘caveolae’ of P vivax and P ovale (with one study suggesting caveole is also found on P malariae IRBCs) (Atkinson and Aikawa, 1990) Our current understanding of these structures is derived mainly from electron microscopy (EM) observations and there... Organization ix List of Symbols LIST OF SYMBOLS ∆G ∆G* ∆H ∆S F kB KD Keq koff kon NB P R r T t voff von xβ τ free energy barrier reduced free energy barrier at the presence of external force thermodynamic enthalpy thermodynamic entropy the force acting on the bond Boltzmann's constant dissociation constant equilibrium constant dissociation rate or off rate association rate or on rate probability of bond survival... probability density function of unbinding force the gas constant loading rate temperature time the natural vibration frequency factor of the dissociation of the bond in vacuum the natural vibration frequency factor of the association of the bond in vacuum Free energy barrier width or mechanical reaction coordinate life time of molecular bond x List of Tables List of Tables Table 2-1 Summary of different surface . ATOMIC FORCE MICROSCOPY STUDY OF MALARIA INFECTED RED BLOOD CELLS LI ANG NATIONAL UNIVERSITY OF SINGAPORE 2008 ATOMIC FORCE MICROSCOPY STUDY OF MALARIA INFECTED. surface of the Plasmodium (P.) spp. infected red blood cells (IRBCs) have a profound importance on the pathobiology of human malaria. Knob-like protrusions have been reported on the surface of P of Cytoadherence of P. falciparum IRBCs 13 1.3 Objective and Scope of This Thesis 24 1.3.1 Objectives 24 1.3.2 Scope of Project 25 CHAPTER 2 ATOMIC FORCE MICROSCOPY AND SINGLE-MOLECULE FORCE

Ngày đăng: 11/09/2015, 14:34

TỪ KHÓA LIÊN QUAN

TÀI LIỆU CÙNG NGƯỜI DÙNG

TÀI LIỆU LIÊN QUAN