Báo cáo khoa học: High negative charge-to-size ratio in polyphosphates and heparin regulates factor VII-activating protease pdf

High negative charge-to-size ratio in polyphosphates and heparin regulates factor VII-activating protease ă ă Lars Muhl1, Sebastian P Galuska1, Katariina Oorni2, Laura Hernandez-Ruiz3, Luminita-Cornelia Andrei-Selmer , Rudolf Geyer , Klaus T Preissner1, Felix A Ruiz3, Petri T Kovanen2 and Sandip M Kanse1 Institute for Biochemistry, Justus-Liebig-University, Giessen, Germany Wihuri Research Institute, Helsinki, Finland Unidad de Investigacion, Hospital Universidad Puerta del Mar and Universidad de Cadiz, Spain Philipps University, Marburg, Germany Keywords FSAP; heparin; mast cells; platelets; polyphosphate Correspondence S M Kanse, Institute for Biochemistry, Justus-Liebig-University Giessen, Friedrichstrasse 24, 35392 Giessen, Germany Fax: +49 641 9947509 Tel: +49 641 9947521 E-mail: sandip.kanse@biochemie.med uni-giessen.de (Received 12 March 2009, revised 28 May 2009, accepted 29 June 2009) doi:10.1111/j.1742-4658.2009.07183.x Factor VII-activating protease (FSAP) circulates as an inactive zymogen in the plasma FSAP also regulates fibrinolysis by activating pro-urokinase or cellular activation via cleavage of platelet-derived growth factor BB (PDGF-BB) As the Marburg I polymorphism of FSAP, with reduced enzymatic activity, is a risk factor for atherosclerosis and liver fibrosis, the regulation of FSAP activity is of major importance FSAP is activated by an auto-catalytic mechanism, which is amplified by heparin To further investigate the structural requirements of polyanions for controlling FSAP activity, we performed binding, activation and inhibition studies using heparin and derivatives with altered size and charge, as well as other glycosaminoglycans Heparin was effective in binding to and activating FSAP in a size- and charge density-dependent manner Polyphosphate was more potent than heparin with regard to its interactions with FSAP Heparin was also an effective co-factor for inhibition of FSAP by plasminogen activator inhibitor (PAI-1) and antithrombin, whereas polyphosphate served as co-factor for the inhibition of FSAP by PAI-1 only For FSAP-mediated inhibition of PDGF-BB-induced vascular smooth muscle cell proliferation, heparin as well as a polyphosphate served as efficient co-factors Native mast cell-derived heparin exhibited identical properties to those of unfractionated heparin Despite the strong effects of synthetic polyphosphate, the platelet-derived material was a weak activator of FSAP Hence, negatively charged polymers with a high charge-to-size ratio are responsible for the activation of FSAP, and also act as co-factors for its inhibition by serine protease inhibitors Introduction Factor VII-activating protease (FSAP) is a serine protease that is predominantly expressed in the liver It circulates as an inactive zymogen with a concentration of 12 lgỈmL)1 in the plasma, and is known to activate factor VII and pro-urokinase [1,2] It was first purified by its ability to bind to hyaluronic acid, and was there- Abbreviations AT, antithrombin; EGF3, epidermal growth factor like-3; FSAP, factor VII-activating protease; PAI-1, plasminogen activator inhibitor 1; PDGF-BB, platelet-derived growth factor BB; PolyP, polyphosphate; SERPIN, serine protease inhibitor; SPR, surface plasmon resonance; TMB, 3,3¢,5,5¢-tetramethylbenzidine; VSMC, vascular smooth muscle cells 4828 FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS L Muhl et al fore designated as hyaluronic acid binding protein (HABP-2) [3] Activation of FSAP requires cleavage between residues R313 and I314, separating the light chain and the heavy chain [4] Negatively charged polyanions such as heparin [4,5], nucleic acids [6,7] and dextran sulfate [4] bind to FSAP This interaction leads to auto-catalytic activation [4,5], followed by auto-proteolysis This propensity to partial proteolysis has been used to determine the domain responsible for binding to heparin and RNA Multiple regions of FSAP contribute to polyanion binding, but the epidermal growth factor like-3 (EGF3) domain with a cluster of positively charged amino acids is particularly important [6] Although FSAP was initially isolated on a hyaluronic acid column [3], no information is available as to how hyaluronic acid can bind to FSAP, nor whether it can activate FSAP [4] The concentration of hyaluronic acid, as well as its transition from the highto low-molecular-weight form, is related to the regulation of angiogenesis, atherosclerosis, restenosis and inflammation [8] FSAP activation is also mediated by nucleic acids, with RNA having a stronger effect than DNA [6,7] Heparin is the most extensively studied polyanion with respect to FSAP function It has been shown that unfractionated heparin is a strong activator of FSAP, but low-molecular-weight heparin has not been systematically tested The role of the more ubiquitous heparan sulfate and other glycosaminoglycans is also not known Polyphosphate (PolyP) is a linear polymer of orthophosphate (Pi) residues linked by high-energy phosphoanhydride bonds, found in many cell types [9] PolyP, with an approximate chain length from 70–75 phosphate units, is stored in platelet-dense granules [10] and released upon platelet activation PolyP can amplify coagulation by activation of the contact factor pathway, as well as activation of factor V, inhibition of the anticoagulant function of tissue factor pathway inhibitor (TFPI), and enhancing the activity of thrombin-activated fibrinolysis inhibitor (TAFI) [11] Once activated, FSAP can be rapidly inhibited by serine protease inhibitors (SERPINs), such as a1-antitrypsin, a2-antiplasmin, antithrombin (AT) and C1 inhibitor [4,12–14], as well as plasminogen activator inhibitor (PAI-1) [15] and protease nexin [16] AT and a2-antiplasmin were shown to be efficient inhibitors in the presence of heparin [4], whereas PAI-1 was shown to be an inhibitor only in the presence of RNA but not heparin [15] The presence of a naturally occurring polymorphism in the FSAP gene leading to an amino acid exchange Polyanions and FSAP (G534E, or Marburg I polymorphism) results in diminished proteolytic activity towards factor VII, prourokinase [17] and PDGF-BB (platelet-derived growth factor BB) [18] The Marburg I polymorphism is associated with a higher risk for carotid stenosis [19], and, in comparison to wild-type FSAP, is not able to inhibit neointima formation in a mouse model [18] Similarly, Marburg I FSAP is associated with advanced liver fibrosis, which may be due to its inability to inhibit PDGF-BB-mediated proliferation of hepatic stellate cells [21] These findings indicate the importance of FSAP enzymatic activity with respect to its function in vivo However, it is not clear which polyanions are relevant for the regulation of FSAP activity This prompted us to investigate the requirements for FSAP interaction with polyanions known to be present in atherosclerotic arterial wall and ⁄ or fibrotic liver, and also to define the molecular basis of the binding, activation and regulation mechanisms Results FSAP binding to polyanions Electrophoretic mobility shift assays were performed to characterize the interaction between FSAP and various polyanions Preincubation of FSAP with unfractionated heparin, low-molecular-weight heparin, PolyP65 or PolyP35 induced a shift in the mobility of FSAP in polyacrylamide gels with or without urea Other polyanions had no influence at all When BSA was used as a control, none of the polyanions induced a shift in the BSA band (Fig 1A) Concentrationdependent analysis indicated that the EC50 was 95 ± nm for the shift with unfractionated heparin and 28 ± nm for PolyP65 (Fig 1B and Figs S1 and S2) To examine whether the various polyanions use the same region in the FSAP molecule for binding, we performed competition binding assays in which binding of biotinylated unfractionated heparin to FSAP was measured (Fig 1C) Unfractionated heparin competed with biotinylated heparin for binding to FSAP, whereas low-molecular-weight heparin showed low competition (Fig 1C, upper panel) PolyP competed for this binding in a chain length-dependent manner All other heparin derivatives, as well as chondroitin sulfate, dermatan sulfate, polysialic acid, heparan sulfate and hyaluronic acid, showed no competition, indicating no binding to FSAP (Fig 1C, lower panel, and Fig S3A) Thus, using gel-shift and competition binding assays, it was demonstrated that binding to FSAP depends on the size and charge density of the macromolecule FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS 4829 Polyanions and FSAP L Muhl et al Fig Binding of FSAP to polyanions (A) FSAP or BSA (5 lg per lane) were preincubated with the respective polyanion (10 lg ⁄ lane) for 30 Samples were directly loaded onto gels containing urea (upper panel) or native polyacrylamide gels (middle and lower panels) Shifted bands (complexed FSAP and polyanions) indicate binding of the particular polyanion to FSAP (B) In a similar experiment to that shown in (A), the concentration of unfractionated heparin and PolyP65 was varied (0.002–2 lM) Complex formation was quantified by densiometric analysis, and the results from three separate experiments were pooled to determine the EC50 values (C) FSAP (10 lgỈmL)1) was immobilized, and heparin derivatives (upper panel) or other polyanions (lower panel) (0.01–100 lgỈmL)1) were mixed with biotinylated heparin albumin (0.5 ngỈmL)1) and added to the plate Detection of bound biotinylated heparin albumin was measured using peroxidase-conjugated streptavidin and 3,3¢,5,5¢tetramethylbenzidine (TMB) substrate (mean ± SEM, n = 4) A B C Fig Increased auto-activation of FSAP by polyanions Polyanions at concentrations in the range 0.01–100 lgỈmL)1 were added to FSAP (1 lgỈmL)1), and FSAP activity (mmODỈmin)1) was determined (mean ± SEM, n = 4) Activation of FSAP by various polyanions We next investigated all the polyanions described above with respect to their ability to activate FSAP 4830 Unfractionated heparin was a strong activator, lowmolecular-weight heparin activated FSAP to a smaller extent, and all other heparin-derivatives exhibited no activation (Fig 2, upper panel) PolyP showed potent activation of FSAP in a chain length-dependent manner There was a 4–6-fold increase in Vmax with unfractionated heparin and PolyP65, with no change in FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS L Muhl et al KM (Fig S2) Heparan sulfate and dermatan sulfate showed weak activation of FSAP at high concentrations (Fig 2, middle panel) Polysialic acid and hyaluronic acid did not activate FSAP (Fig 2, lower panel) N-acetyl heparin, de-N-sulfated heparin, N-acetyl-de-O-sulfated heparin, polysialic acid and hyaluronic acid totally failed to increase FSAP activity To assess the specificity of the PolyP effect, it was degraded using calf intestinal phosphatase, which is also a highly active exopolyphosphatase [11] The accelerating effect of PolyP on FSAP activity was decreased by phosphatase pretreatment in a time- and dose-dependent manner (Fig S4) As a control, we observed that phosphatase treatment did not influence unfractionated heparin-mediated activation of FSAP (Fig S4) Hence, the effect of PolyP was not due to a contaminant These studies show that the pattern of binding of polyanions to FSAP is identical to the pattern of their ability to activate FSAP Polyanions and FSAP A B Polyanions as co-factors for the inhibition of FSAP by PAI-1 and AT SERPINs exhibit enhanced or altered substrate specificity in the presence of heparin or other co-factors [22] To examine the co-factor function of polyanions with respect to FSAP inhibition, active two-chain FSAP was preincubated with PAI-1 or AT with or without various concentrations of polyanions Inhibition of FSAP by PAI-1 was increased by unfractionated heparin, lowmolecular-weight heparin and to a lower extent by N-acetyl heparin (Fig 3A, upper panel) PolyP exhibits strong co-factor function for the inhibition of FSAP by PAI-1 in a chain length-dependent manner The IC50 of PAI-1 for the inhibition of FSAP was halved by unfractionated heparin and PolyP65 (Fig S5) Heparan sulfate was a co-factor at high concentrations (Fig 3A, lower panel), and dermatan sulfate and polysialic acid C Fig Inhibition of FSAP by PAI-1 and AT; co-factor function of polyanions FSAP (1 lgỈmL)1) was preincubated either with PAI-1 (1 lgỈmL)1) (A) or with AT (5 lgỈmL)1) (B) for 30 with or without heparin derivatives (upper panels) or other polyanions (lower panels) in the concentration range 0.01–100 lgỈmL)1 FSAP activity (mmODỈmin)1) was determined, and inhibition was calculated as a percentage of FSAP activity without inhibitor (mean ± SEM, n = 4) (C) SPR sensograms showing the association and dissociation of FSAP–inhibitor complexes in the presence of polyanions FSAP (10 lgỈmL)1) was bound to a specific high-affinity antibody to FSAP, immobilized on a CM5 sensor chip, prior to injection of either AT (5 lgỈmL)1) or PAI-1 (5 lgỈmL)1), alone (control) or in the presence of polyphosphate 65 (10 lgỈmL)1) or unfractionated heparin (10 lgỈmL)1) Alignment of SPR sensograms was performed using the program BIAevaluation 3.2 RC1 FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS 4831 Polyanions and FSAP L Muhl et al at even higher concentrations (Fig S3B), but hyaluronic acid had no effect at all (Fig 3A, lower panel) In the case of FSAP inhibition by AT, only unfractionated heparin and heparan sulfate were able to serve as co-factors (Fig 3B) PolyP and other tested polyanions showed no co-factor properties for the ATdependent FSAP inhibition (Fig 3B, lower panel and Fig S3C) The activity of FSAP was increased by lowmolecular-weight heparin, N-acetyl heparin (Fig 3B, upper panel) and PolyP (Fig 3B, lower panel) even in the presence of AT To consolidate these findings, real-time interaction studies were performed using surface plasmon resonance (SPR) These results confirm that FSAP interacts with AT only in the presence of unfractionated heparin (KA of  2.9 · 107 [1 ⁄ M]) but not in the presence of PolyP In contrast, FSAP interacts with PAI-1 without a co-factor (KA of  1.6 · 107 [1 ⁄ M]) in the presence of unfractionated heparin (KA of  3.2 · 107 [1 ⁄ M]) as well as in the presence of PolyP (KA of  97 · 107 [1 ⁄ M]) (Fig 3C) Hence, polyanions can selectively promote inhibition of the enzymatic activity of FSAP Polyanions as co-factors for the FSAP-dependent inhibition of VSMC proliferation A major function of FSAP is the specific proteolytic cleavage and inactivation of PDGF-BB [23], and this process is enhanced by heparin and RNA [24] We observed that low-molecular-weight heparin and heparan sulfate also increase the inhibitory effect of FSAP on proliferation of vascular smooth muscle cells (VSMC), but to a lower extent compared to unfractionated heparin PolyP also promoted the inhibitory effect of FSAP on VSMC proliferation, whereas de-Nsulfated heparin and hyaluronic acid were ineffective (Fig 4) The ability of each polyanion to inhibit cell proliferation matched the respective pattern of FSAP binding and activation Assessment of mast cell heparin and platelet PolyP as co-factors for FSAP function Mast cell-derived macromolecular heparin and platelet-derived PolyP were isolated as native substances and tested for their interaction with FSAP The mast cell-derived heparin bound to FSAP, as indicated by a mobility shift in native polyacrylamide gels (Fig 5A, upper panel) When compared to unfractionated heparin, mast cell heparin was even more efficient with respect to competition of biotinylated heparin binding to immobilized FSAP (Fig 5A, middle panel) and FSAP activation (Fig 5B, upper panel) 4832 no PDGF-BB or FSAP or polyanion with PDGF-BB and no FSAP or polyanion Buffer FSAP Fig Polyanion-dependent amplification of the inhibitory effect of FSAP on VSMC activation PDGF-BB (20 ngỈmL)1) was preincubated without (light gray columns) or with (dark gray columns) FSAP (15 lgỈmL)1) and ⁄ or 10 lgỈmL)1 of the various polyanions for h at 37°C in serum-free medium Subsequently, VSMC were stimulated for 36 h in medium containing 0.2% fetal calf serum DNA synthesis was measured (mean ± SD, n = 3) using a kit that detects BrdU incorporation into newly synthesized DNA In mobility shift assays, platelet-derived PolyP bound to FSAP weakly (Fig 5A, upper panel) However, it competed with biotinylated heparin for binding to immobilized FSAP more strongly than its synthetic analogue PolyP65 did (Fig 5A, lower panel) Unexpectedly, activation of FSAP by native platelet-derived PolyP was much lower when compared to the synthetic material (Fig 5B, lower panel) Thus, mast cell-derived heparin was identical to unfractionated heparin for all aspects investigated, but there were differences between platelet-derived and synthetic PolyP Discussion Genetic studies show that the presence of the Marburg I single-nucleotide polymorphism is a risk factor for carotid stenosis [19] and liver fibrosis [20] This isoform of FSAP exhibits reduced enzymatic activity [17], indicating that the local proteolytic activity of FSAP may play a crucial role in development of the disease state Therefore, it is important to understand the regulation of FSAP activity in order to define its pathophysiological role Polyanions have been shown to play a key role in regulating FSAP activity by promoting auto-catalytic activation In the present study, we systematically characterized the effects of various polyanions on FSAP activity FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS L Muhl et al Polyanions and FSAP te rin pa A fra Un he on cti d ate st Ma in ar ll ce p he te ho sp ho lyp Po sp 65 let p oly p ate Pl Complexed FSAP Competition with heparin-albumin-biotin (%) Free FSAP 120 80 40 –40 Mast cell heparin Unfractionated heparin // // 0.1 Heparin (µg·mL–1) 10 120 80 40 // // –40 Platelet polyphosphate Polyphosphate 65 // 0.1 10 Polyphosphate (µg·mL–1) B Mast cell heparin Unfractionated heparin 20 FSAP-activity (mmOD·min–1 at 405 nm) 15 10 // // 20 0.1 0.01 Heparin (µg·mL–1) 10 Polyphosphate 65 Platelet polyphosphate 15 10 // // Fig Properties of mast cell-derived heparin and platelet-derived PolyP with respect to FSAP (A) Upper panel: FSAP (5 lg per lane) was preincubated with unfractionated heparin (UH), mast cellderived heparin, PolyP65 or platelet-derived PolyP (each lg per lane), and loaded directly onto native polyacrylamide gel Shifted bands (complexed FSAP) indicate binding of the respective polyanion to FSAP Middle and lower panels: FSAP (10 lgỈmL)1) was immobilized, and synthetic or mast cell-derived heparin (0.05– 10 lgỈmL)1) and synthetic or platelet-derived PolyP (0.033– lgỈmL)1) were mixed with biotinylated heparin albumin (0.5 ngỈmL)1) and added to the plate The amount of bound biotinylated heparin albumin was measured using peroxidase-conjugated streptavidin and TMB substrate (mean ± SD, n = 3) (B) Unfractionated heparin (0.01–10 lgỈmL)1), mast cell-derived heparin (0.02– lgỈmL)1) (upper panel) or synthetic or platelet-derived PolyP (0.01–2.5 lgỈmL)1) (lower panel) were added to FSAP (1 lgỈmL)1), and FSAP activity (mmODỈmin)1) was determined (mean ± SD, n = 3) 0.01 0.1 Polyphosphate (µg·mL–1) 10 lower potential for binding to and activating FSAP The heparin homologues N-acetyl heparin, de-N-sulfated heparin and N-acetyl-de-O-sulfated heparin, which have the same size but reduced negative charge, neither bind to nor activate FSAP (Fig 6) The proteoglycan heparan sulfate has an even lower negative charge, compared to unfractionated heparin, and exhibits weak FSAP binding and activation Mast cell-derived heparin has a higher charge than unfractionated heparin, and exhibits a stronger ability to bind to and activate FSAP [25] Chondroitin sulfate, dermatan sulfate and polysialic acid also have a less negative charge density than unfractionated heparin and show no FSAP binding or activation potential (Fig 6) FSAP was first purified based on its binding to hyaluronic acid [3] In the present study, we demonstrate that there is no tight interaction between hyaluronic acid and FSAP, most likely due to the relatively low negative charge density in the polyanion Its isolation on hyaluronic acid columns could be due to altered physical properties of immobilized hyaluronic acid The significance of these results is that the very ubiquitous heparan sulfate proteoglycans and other matrix-associated glycosaminoglycans play no role in the regulation of FSAP activity This is rather related to the proximity and activation state of mast cells that secrete heparin, such as in atherosclerotic plaques [26] Polyphosphate Heparin and other glycosaminoglycans The binding to FSAP and the subsequent activation of FSAP by heparin depends on its size and overall negative charge Low-molecular-weight heparin exhibits PolyP was a more potent activator of FSAP than heparin PolyP65 was the most active form of PolyP, with smaller forms showing diminished activity Degradation by phosphatases decreased its properties with FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS 4833 Polyanions and FSAP L Muhl et al Fig Structure of the various polyanions used in the study Potential modifications of the sugar residues by sulfate groups are shown The mean numbers of sulfate groups per disaccharide unit (DS) are given for all glycosaminoglycans The mean acid dissociation constants (pKa values) for the phosphate, sulfate and carboxyl groups are 1.5, 2.0 and 4.7, respectively [37,38] respect to FSAP binding and activation, and any influence on FSAP activity was completely neutralized In order to put these findings in a pathophysiological context, we compared the activity of synthetic PolyP with that of native platelet-derived material Platelet-derived PolyP exhibited quite anomalous properties compared to synthetic PolyP In gel-shift assays, it demonstrated weak binding, but was as efficient as synthetic PolyP in 4834 competing for heparin binding to FSAP Native PolyP was a very weak activator of FSAP compared to the synthetic version One reason for this discrepancy between synthetic and native PolyP could be that synthetic PolyP65 is a heterogeneous mixture, with polymers up to 200 units, whereas native PolyP is extremely pure and has a more homogeneous size with 70–75 units [10,27] In addition to their difference in FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS L Muhl et al size, we cannot exclude the possibility of a contaminant that has a confounding effect on the interaction of native PolyP with FSAP No comparable data exist in the literature, as this is one of the first studies to compare the activities of synthetic with platelet-derived PolyP Given the robust activity of synthetic PolyP, the role of endogenous platelet-derived material needs to be investigated further Inhibition SERPINs such as protease nexin and PAI-1 can efficiently inhibit FSAP Whereas protease nexin inhibits proteases independently of any co-factor [16], PAI-1 is known to require heparin as a co-factor for inhibition of some of its targets such as thrombin [28] The co-factor effect of heparin is due to a change in the conformation of the SERPIN as well as the ability of heparin to co-join the protease with the inhibitor Previously published data showed that heparin was not a co-factor for PAI-1-dependent inhibition of FSAP [15] In this study, we demonstrate that both heparin and polyphosphate are potent co-factors for the inhibition of FSAP by PAI-1 A reduction in size and charge density in heparin led to lower inhibition of FSAP by PAI-1 AT inhibits FSAP only in the presence of heparin but not PolyP The size and negative charge of heparin has an even greater importance for the interaction with AT, as indicated by the fact that lowmolecular-weight heparin and N-acetyl heparin promote an increase in FSAP activity rather than inhibiting it Thus, polyanion binding to SERPINs, over and above their binding to FSAP, plays a decisive role in mediating its inhibition PolyP increased the inhibition of FSAP by PAI-1 but not by AT Whereas heparin changes the tertiary structure of AT [29], PolyP was shown to be unable to induce any conformational changes in AT, as determined by measurement of the intrinsic protein fluorescence of AT incubated with PolyP (F A Ruiz, unpublished results) Both polyanions decreased the IC50 for the inhibition of FSAP by PAI-1 twofold SERPINs inhibit their target protease by a suicide substrate mechanism that involves a : formation of an irreversible covalent complex [30] Only protease-inactive mutants show reversible binding to SERPINs [30], and the FSAP–PAI-1 complex demonstrated some dissociation in our experiments (Fig 3C), indicating some deviation from the classical model of protease–inhibitor interactions Hence, the overall inhibition of FSAP depends not only on the inhibitor but also on the presence of an appropriate co-factor in the vicinity of FSAP Polyanions and FSAP Conclusions The two major polyanions, heparin and PolyP, use the same binding region in the FSAP molecule, as revealed by the competition binding assay Charge density, size and also conformational flexibility determine the affinity of this interaction Other matrixderived polyanions were not effective Binding to polyanions was also observed in the presence of a strong denaturant, urea, indicating a strong charge interaction The region of FSAP that is probably responsible for this binding is the EGF3 domain, which contains a positively charged cluster of amino acids, although other regions of FSAP promote this interaction [6] Using a recombinant EGF3 domain deletion mutant of FSAP, no activation of FSAP was obtained with either heparin or with PolyP [31], further confirming the involvement of this region in polyanion binding and activation Polyanions strongly reduced the proliferative activity of PDGFBB in the presence of FSAP This could explain the influence of polyanions such as heparin on smooth muscle proliferation in vivo [32], and a similar function is expected for PolyP As a lowering in FSAP activity is correlated with diseases [19,20], these new insights into the regulation of FSAP activity will lead to increased understanding of FSAP function under physiological und pathophysiological conditions Identification of specific size, sequence and charge requirements may allow rational design of polyanions with higher specificity for the regulation of FSAP activity Experimental procedures Materials FSAP was isolated as described previously [5] PolyP 65-mer (molecular mass  6.6 · 103 Da) and PolyP 15-mer (molecular mass  1.5 · 103 Da) were obtained from Sigma (Munich, Germany), and PolyP 35-mer (molecular mass  3.5 · 103 Da) was obtained from Roth (Karlsruhe, Germany) Unfractionated heparin (molecular mass  15 · 103 Da), heparan sulfate, dermatan sulfate, chondroitin sulfate C, low-molecular-weight heparin (molecular mass  · 103 Da), N-acetyl heparin, de-N-sulfated heparin and N-acetyl-de-O-sulfated heparin (all molecular masses hyaluronic acid (molecular mass  15 · 103 Da),  · 105 Da) from human placenta or rooster comb and biotinylated heparin albumin were obtained from Sigma Polysialic acid (molecular mass £ 38 · 103 Da) was separated from oligosialic acid as described previously [33] Calf intestinal alkaline phosphatase was obtained from Fermentas FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS 4835 Polyanions and FSAP L Muhl et al (St Leon-Rot, Germany) PAI-1 was generously provided by Dr Paul Declerck (Katholieke Universiteit, Leuven, Belgium) AT was obtained from CSL Behring (Marburg, Germany) Isolation of platelet-derived PolyP and mast cell-derived macromolecular heparin FSAP enzyme activity assay Platelet homogenates were prepared as described previously [34] After centrifugation at 19 000 g, the pellet was used to extract native PolyP using perchloric acid [10] PolyP was further purified on an OMIX C18 100 lL tip (Varian, Lake Forest, CA) before use Native macromolecular heparin (molecular mass 75 · 104 Da; range · 105–1 · 106) was purified from granule remnants of rat serosal mast cells, as described previously [35] Briefly, granule remnants were treated with m KCl to release heparin-bound molecules (notably chymase and other proteases) from heparin proteoglycans and to disintegrate the granule remnants into heparin proteoglycan monomers [36] The incubation mixture was then applied to a Sephacryl S-200 column (GE Healthcare Life Sciences, Uppsala, Sweden) column for isolation and separation of heparin proteoglycans The residual chymase activity in the heparin proteoglycan fraction was inhibited using phenylmethanesulfonyl fluoride Electrophoretic mobility shift assays to detect polyanion binding to FSAP Polyacrylamide–bisacrylamide (37.5:1) native gels (6–10%) were poured with Tris ⁄ borate ⁄ EDTA (TBE) (90 mm Tris, 90 mm boric acid, mm EDTA, pH 8.3), with or without 6.7 m urea, in a horizontal gel chamber FSAP (5 lg) was preincubated for 30 with or without respective polyanions (10 lg), native sample buffer (TBE with sucrose and bromphenol blue) was added, and samples were loaded onto the gel After separation, the gel was stained either with toluidine blue to visualize polyanions (not shown) or with Coomassie brilliant blue to visualize proteins Densiometric analysis was performed to determine the affinity of these interactions Competition of heparin binding to immobilized FSAP with various polyanions Microtiter plates were coated with 50 lL of a 10 lgỈmL)1 FSAP solution in 100 mm sodium carbonate (pH 9.5) overnight at 4°C Wells were washed, and non-specific binding sites were blocked with NaCl/Tris (25 mm Tris ⁄ HCl, pH 7.5, 150 mm NaCl) containing 3% w ⁄ v BSA for h Biotinylated heparin albumin (0.5 ngỈmL)1) mixed with dilutions of polyanions was allowed to bind for h at room temperature in NaCl/Tris containing 0.1% w ⁄ v BSA, after which the plates were washed three times with NaCl/Tris containing 0.1% w ⁄ v Tween-20 (NaCl/Tris-T) Bound biotinylated 4836 heparin albumin was detected using peroxidase-conjugated streptavidin (DAKO, Glostrup, Denmark) and an immunopure TMB substrate kit (Thermo Fischer Scientific, Rockford, IL, USA) FSAP activity assays were performed as described previously [16] In brief, microtiter plates were blocked with NaCl/Tris containing 3% w ⁄ v BSA for h, and washed with NaCl/ Tris-T The standard assay system consisted of NaCl/Tris, lgỈmL)1 FSAP and 0.2 mm of the chromogenic substrate S-2288 (H-d-isoleucyl-l-prolyl-l-arginine-p-nitroanilinedihydrochloride) (Haemochrome, Essen, Germany) and was followed over a period of 60 at 37°C at 405 nm in an EL 808 microplate reader (BioTek Instruments, Winooski, VT, USA) If an inhibitor was used, this was added together with FSAP to the plates with and without polyanionic co-factor 30 before adding the chromogenic substrate Characterization of FSAP–inhibitor interaction using surface plasmon resonance (SPR) technology Immobilization on sensor chips, and association and dissociation of interacting biomolecules, were followed in real time by monitoring the change in SPR signal expressed in resonance units (RU) All experiments were performed at 25°C To prepare the sensor chip surface, antibodies to FSAP or isotype controls were immobilized on a CM5 research-grade chip (Biacore/GE Healthcare, Freiburg, Germany) at 10 000 RU, via amino coupling (Biacore) and using HBS-N (20 mm Hepes, pH 7.4, 100 mm NaCl), as running buffer Interaction analysis experiments were performed at a flow rate of 20 lLỈmin)1 using HBS-P [20 mm Hepes, pH 7.4, 100 mm NaCl, 0.05% Surfactant P20 (Biacore cat.nr.:BR-1000-54)] supplemented with mm CaCl2 as running buffer FSAP (25 lL, 10 lgỈmL)1) was captured on the immobilized antibodies, and then AT or PAI-1 (25 lL, 0–5 lgỈmL)1) were injected alone and in the presence of unfractionated heparin or PolyP (10 lgỈmL)1) Sensorgrams were analyzed using BIAevaluation software version 3.2 RC1 Kinetic constants were obtained using the Langmuir binding model 1:1 Cell culture Mouse vascular smooth muscle cells (VSMC) were cultured in Iscove’s modified medium (Invitrogen, Karlsruhe, Germany) with 10% v ⁄ v fetal calf serum (HyClone, Logan, UT, USA), 10 mL)1 penicillin, 10 lgỈmL)1 streptomycin, mm l-glutamine and mm sodium pyruvate (Invitrogen) Cells were growth-arrested in serum-free medium for 18 h prior to experiments FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS L Muhl et al Polyanions and FSAP DNA synthesis assays VSMC were stimulated for 36 h with the test substances in medium containing 0.2% fetal calf serum For the last 24 h, 5-bromo-2-deoxyuridine (BrdU) was added, and the cells were processed using a BrdU detection kit (Roche Diagnostics, Mannheim, Germany) as described by the manufacturer 10 Acknowledgements The assistance of Susanne Tannert-Otto is greatly appreciated We are grateful to Dr Paul Declerck (Department of Pharmaceutical Sciences, Katholieke Universiteit, Leuven, Belgium) for providing PAI-1 This study was financed by a grant from the Deutsche Forschungsgemeinschaft to S.M.K (SFB 547: C14) Wihuri Research Institute is maintained by the Jenny and Antti Wihuri Foundation (Helsinki, Finland) References Romisch J (2002) Factor VII activating protease (FSAP): a novel protease in hemostasis Biol Chem 383, 1119–1124 Kanse SM, Parahuleva M, Muhl L, Kemkes-Matthes B, Sedding D & Preissner KT (2008) Factor VII-activating protease (FSAP): vascular functions and role in atherosclerosis Thromb Haemost 99, 286–289 Choi-Miura NH, Tobe T, Sumiya J, Nakano Y, Sano Y, Mazda T & Tomita M (1996) Purification and characterization of a novel hyaluronan-binding protein (PHBP) from human plasma: it has three EGF, a kringle and a serine protease domain, similar to hepatocyte growth factor activator J Biochem 119, 1157–1165 Etscheid M, Hunfeld A, Konig H, Seitz R & Dodt J (2000) Activation of proPHBSP, the zymogen of a plasma hyaluronan binding serine protease, by an intermolecular autocatalytic mechanism Biol Chem 381, 1223–1231 Kannemeier C, Feussner A, Stohr HA, Weisse J, Preissner KT & Romisch J (2001) Factor VII and single-chain plasminogen activator-activating protease: activation and autoactivation of the proenzyme Eur J Biochem 268, 3789–3796 Altincicek B, Shibamiya A, Trusheim H, Tzima E, Niepmann M, Linder D, Preissner KT & Kanse SM (2006) A positively charged cluster in the epidermal growth factor-like domain of Factor VII-activating protease (FSAP) is essential for polyanion binding Biochem J 394, 687–692 Nakazawa F, Kannemeier C, Shibamiya A, Song Y, Tzima E, Schubert U, Koyama T, Niepmann M, Trusheim H, Engelmann B et al (2005) Extracellular RNA is a natural cofactor for the (auto-)activation of 11 12 13 14 15 16 17 18 19 Factor VII-activating protease (FSAP) Biochem J 385, 831–838 Jiang D, Liang J & Noble PW (2007) Hyaluronan in tissue injury and repair Annu Rev Cell Dev Biol 23, 435–461 Brown MR & Kornberg A (2004) Inorganic polyphosphate in the origin and survival of species Proc Natl Acad Sci USA 101, 16085–16087 Ruiz FA, Lea CR, Oldfield E & Docampo R (2004) Human platelet dense granules contain polyphosphate and are similar to acidocalcisomes of bacteria and unicellular eukaryotes J Biol Chem 279, 44250–44257 Smith SA, Mutch NJ, Baskar D, Rohloff P, Docampo R & Morrissey JH (2006) Polyphosphate modulates blood coagulation and fibrinolysis Proc Natl Acad Sci USA 103, 903–908 Choi-Miura NH, Saito K, Takahashi K, Yoda M & Tomita M (2001) Regulation mechanism of the serine protease activity of plasma hyaluronan binding protein Biol Pharm Bull 24, 221–225 Hunfeld A, Etscheid M, Konig H, Seitz R & Dodt J (1999) Detection of a novel plasma serine protease during purification of vitamin K-dependent coagulation factors FEBS Lett 456, 290–294 Romisch J, Vermohlen S, Feussner A & Stohr H (1999) The FVII activating protease cleaves single-chain plasminogen activators Haemostasis 29, 292–299 Wygrecka M, Morty RE, Markart P, Kanse SM, Andreasen PA, Wind T, Guenther A & Preissner KT (2007) Plasminogen activator inhibitor-1 is an inhibitor of factor VII-activating protease in patients with acute respiratory distress syndrome J Biol Chem 282, 21671– 21682 Muhl L, Nykjaer A, Wygrecka M, Monard D, Preissner KT & Kanse SM (2007) Inhibition of PDGF-BB by Factor VII-activating protease (FSAP) is neutralized by protease nexin-1, and the FSAP–inhibitor complexes are internalized via LRP Biochem J 404, 191–196 Roemisch J, Feussner A, Nerlich C, Stoehr HA & Weimer T (2002) The frequent Marburg I polymorphism impairs the pro-urokinase activating potency of the factor VII activating protease (FSAP) Blood Coagul Fibrinolysis 13, 433–441 Sedding D, Daniel JM, Muhl L, Hersemeyer K, Brunsch H, Kemkes-Matthes B, Braun-Dullaeus RC, Tillmanns H, Weimer T, Preissner KT et al (2006) The G534E polymorphism of the gene encoding the factor VII-activating protease is associated with cardiovascular risk due to increased neointima formation J Exp Med 203, 2801–2807 Willeit J, Kiechl S, Weimer T, Mair A, Santer P, Wiedermann CJ & Roemisch J (2003) Marburg I polymorphism of factor VII-activating protease: a prominent risk predictor of carotid stenosis Circulation 107, 667–670 FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS 4837 Polyanions and FSAP L Muhl et al 20 Wasmuth HE, Tag CG, Van deLeurE, Hellerbrand C, Mueller T, Berg T, Puhl G, Neuhaus P, Samuel D, Trautwein C et al (2008) The Marburg I variant (G534E) of the factor VII-activating protease determines liver fibrosis in hepatitis C infection by reduced proteolysis of platelet-derived growth factor BB Hepatology 49, 775–780 21 Roderfeld M, Weiskirchen R, Atanasova S, Gressner AM, Preissner KT, Roeb E & Kanse SM (2008) Altered factor VII activating protease expression in murine hepatic fibrosis and its influence on hepatic stellate cells Liver Int 29, 686–691 22 Edelberg JM, Reilly CF & Pizzo SV (1991) The inhibition of tissue type plasminogen activator by plasminogen activator inhibitor-1 The effects of fibrinogen, heparin, vitronectin, and lipoprotein(a) J Biol Chem 266, 7488–7493 23 Kannemeier C, Al-Fakhri N, Preissner KT & Kanse SM (2004) Factor VII-activating protease (FSAP) inhibits growth factor-mediated cell proliferation and migration of vascular smooth muscle cells FASEB J 18, 728–730 24 Shibamiya A, Muhl L, Tannert-Otto S, Preissner KT & Kanse SM (2007) Nucleic acids potentiate Factor VII-activating protease (FSAP)-mediated cleavage of platelet-derived growth factor-BB and inhibition of vascular smooth muscle cell proliferation Biochem J 404, 45–50 25 Alter SC, Metcalfe DD, Bradford TR & Schwartz LB (1987) Regulation of human mast cell tryptase Effects of enzyme concentration, ionic strength and the structure and negative charge density of polysaccharides Biochem J 248, 821–827 26 Kovanen PT (2007) Mast cells: multipotent local effector cells in atherothrombosis Immunol Rev 217, 105–122 27 Clark JE & Wood HG (1987) Preparation of standards and determination of sizes of long-chain polyphosphates by gel electrophoresis Anal Biochem 161, 280–290 28 Ehrlich HJ, Gebbink RK, Keijer J, Linders M, Preissner KT & Pannekoek H (1990) Alteration of serpin specificity by a protein cofactor Vitronectin endows plasminogen activator inhibitor with thrombin inhibitory properties J Biol Chem 265, 13029–13035 29 Olson ST & Shore JD (1981) Binding of high affinity heparin to antithrombin III Characterization of the protein fluorescence enhancement J Biol Chem 256, 11065–11072 30 Rezaie AR (2006) Pentasaccharide enhances the inactivation of factor Xa by antithrombin by promoting the assembly of a Michaelis-type intermediate complex Demonstration by rapid kinetic, surface plasmon resonance, and competitive binding studies Biochemistry 45, 5324–5329 4838 31 Muhl L, Hersemeyer K, Preissner KT, Weimer T & Kanse SM (2009) Structure–function analysis of factor VII activating protease (FSAP): sequence determinants for heparin binding and cellular functions FEBS Lett 583, 1994–1998 32 Garg HG, Cindhuchao N, Quinn DA, Hales CA, Thanawiroon C, Capila I & Linhardt RJ (2002) Heparin oligosaccharide sequence and size essential for inhibition of pulmonary artery smooth muscle cell proliferation Carbohydr Res 337, 2359–2364 33 Galuska SP, Geyer R, Muhlenhoff M & Geyer H (2007) Characterization of oligo- and polysialic acids by MALDI-TOF-MS Anal Chem 79, 7161–7169 34 Hernandez-Ruiz L, Valverde F, Jimenez-Nunez MD, Ocana E, Saez-Benito A, Rodriguez-Martorell J, Bohorquez JC, Serrano A & Ruiz FA (2007) Organellar proteomics of human platelet dense granules reveals that 14-3-3f is a granule protein related to atherosclerosis J Proteome Res 6, 4449–4457 35 Lindstedt L, Lee M & Kovanen PT (2001) Chymase bound to heparin is resistant to its natural inhibitors and capable of proteolyzing high density lipoproteins in aortic intimal fluid Atherosclerosis 155, 87–97 36 Lindstedt L, Lee M, Castro GR, Fruchart JC & Kovanen PT (1996) Chymase in exocytosed rat mast cell granules effectively proteolyzes apolipoprotein AI-containing lipoproteins, so reducing the cholesterol efflux-inducing ability of serum and aortic intimal fluid J Clin Invest 97, 2174–2182 37 Gallagher JT & Walker A (1985) Molecular distinctions between heparan sulphate and heparin Analysis of sulphation patterns indicates that heparan sulphate and heparin are separate families of N-sulphated polysaccharides Biochem J 230, 665–674 38 Miller MJ, Costello CE, Malmstrom A & Zaia J (2006) A tandem mass spectrometric approach to determination of chondroitin ⁄ dermatan sulfate oligosaccharide glycoforms Glycobiology 16, 502–513 Supporting information The following supplementary material is available: Fig S1 Analysis of the binding between FSAP and polyanions using electrophoretic mobility shift assay Fig S2 Determination of the kinetic constants for FSAP Fig S3 Interaction of polysialic acid or dermatan sulfate with FSAP Fig S4 Inhibition of the effect of PolyP by phosphatase Fig S5 Determination of the IC50 value for PAI-1mediated inhibition of FSAP FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS L Muhl et al This supplementary material can be found in the online article Please note: As a service to our authors and readers, this journal provides supporting information supplied by the authors Such materials are peer- Polyanions and FSAP reviewed and may be re-organized for online delivery, but are not copy-edited or typeset Technical support issues arising from supporting information (other than missing files) should be addressed to the authors FEBS Journal 276 (2009) 4828–4839 ª 2009 The Authors Journal compilation ª 2009 FEBS 4839 ... lowmolecular-weight heparin and N-acetyl heparin promote an increase in FSAP activity rather than inhibiting it Thus, polyanion binding to SERPINs, over and above their binding to FSAP, plays a decisive role in. .. unfractionated heparin, and exhibits weak FSAP binding and activation Mast cell-derived heparin has a higher charge than unfractionated heparin, and exhibits a stronger ability to bind to and activate... competition binding assays in which binding of biotinylated unfractionated heparin to FSAP was measured (Fig 1C) Unfractionated heparin competed with biotinylated heparin for binding to FSAP, whereas