Novel interaction of properdin and coagulation factor XI: Crosstalk between complement and coagulation
2022; Elsevier BV; Volume: 6; Issue: 4 Linguagem: Inglês
10.1002/rth2.12715
ISSN2475-0379
AutoresSamantha L. Heal, Lewis Hardy, Clare Wilson, Majid Ali, Robert A. S. Ariëns, Richard Foster, Helen Philippou,
Tópico(s)Mast cells and histamine
ResumoResearch and Practice in Thrombosis and HaemostasisVolume 6, Issue 4 e12715 ORIGINAL ARTICLEOpen Access Novel interaction of properdin and coagulation factor XI: Crosstalk between complement and coagulation Samantha L. Heal BSc, PhD, Corresponding Author Samantha L. Heal BSc, PhD samantha.heal1@nhs.net @SamanthaLHeal orcid.org/0000-0001-9355-8414 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK Correspondence Samantha L. Heal, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: samantha.heal1@nhs.net Helen Philippou, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: h.philippou@leeds.ac.ukSearch for more papers by this authorLewis J. Hardy BSc, PhD, Lewis J. Hardy BSc, PhD @LewisJHardy orcid.org/0000-0002-3567-3518 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorClare L. Wilson BSc, PhD, Clare L. Wilson BSc, PhD orcid.org/0000-0002-2226-0028 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorMajid Ali BSc, PhD, Majid Ali BSc, PhD orcid.org/0000-0001-8365-252X Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorRobert A. S. Ariëns BSc, PhD, Robert A. S. Ariëns BSc, PhD @RobertAriens orcid.org/0000-0002-6310-5745 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorRichard Foster BSc, PhD, Richard Foster BSc, PhD orcid.org/0000-0002-2361-3884 School of Chemistry, University of Leeds, Leeds, UKSearch for more papers by this authorHelen Philippou BSc, PhD, Corresponding Author Helen Philippou BSc, PhD h.philippou@leeds.ac.uk @EleniP3 orcid.org/0000-0002-9199-4201 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK Correspondence Samantha L. Heal, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: samantha.heal1@nhs.net Helen Philippou, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: h.philippou@leeds.ac.ukSearch for more papers by this author Samantha L. Heal BSc, PhD, Corresponding Author Samantha L. Heal BSc, PhD samantha.heal1@nhs.net @SamanthaLHeal orcid.org/0000-0001-9355-8414 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK Correspondence Samantha L. Heal, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: samantha.heal1@nhs.net Helen Philippou, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: h.philippou@leeds.ac.ukSearch for more papers by this authorLewis J. Hardy BSc, PhD, Lewis J. Hardy BSc, PhD @LewisJHardy orcid.org/0000-0002-3567-3518 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorClare L. Wilson BSc, PhD, Clare L. Wilson BSc, PhD orcid.org/0000-0002-2226-0028 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorMajid Ali BSc, PhD, Majid Ali BSc, PhD orcid.org/0000-0001-8365-252X Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorRobert A. S. Ariëns BSc, PhD, Robert A. S. Ariëns BSc, PhD @RobertAriens orcid.org/0000-0002-6310-5745 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UKSearch for more papers by this authorRichard Foster BSc, PhD, Richard Foster BSc, PhD orcid.org/0000-0002-2361-3884 School of Chemistry, University of Leeds, Leeds, UKSearch for more papers by this authorHelen Philippou BSc, PhD, Corresponding Author Helen Philippou BSc, PhD h.philippou@leeds.ac.uk @EleniP3 orcid.org/0000-0002-9199-4201 Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK Correspondence Samantha L. Heal, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: samantha.heal1@nhs.net Helen Philippou, Discovery and Translational Science Department, Leeds Institute of Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK. Email: h.philippou@leeds.ac.ukSearch for more papers by this author First published: 24 May 2022 https://doi.org/10.1002/rth2.12715 Handling Editor: Dr Henri Spronk AboutSectionsPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Abstract Background Evidence of crosstalk between the complement and coagulation cascades exists, and dysregulation of either pathway can lead to serious thromboinflammatory events. Both the intrinsic pathway of coagulation and the alternative pathway of complement interact with anionic surfaces, such as glycosaminoglycans. Hitherto, there is no evidence for a direct interaction of properdin (factor P [FP]), the only known positive regulator of complement, with coagulation factor XI (FXI) or activated FXI (FXIa). Objectives The aim was to investigate crosstalk between FP and the intrinsic pathway and the potential downstream consequences. Methods Chromogenic assays were established to characterize autoactivation of FXI in the presence of dextran sulfate (DXS), enzyme kinetics of FXIa, and the downstream effects of FP on intrinsic pathway activity. Substrate specificity changes were investigated using SDS-PAGE and liquid chromatography–mass spectrometry (LC-MS). Surface plasmon resonance (SPR) was used to determine direct binding between FP and FXIa. Results/Conclusions We identified a novel interaction of FP with FXIa resulting in functional consequences. FP reduces activity of autoactivated FXIa toward S-2288. FXIa can cleave FP in the presence of DXS, demonstrated using SDS-PAGE, and confirmed by LC-MS. FXIa can cleave factor IX (FIX) and FP in the presence of DXS, determined by SDS-PAGE. DXS alone modulates FXIa activity, and this effect is further modulated by FP. We demonstrate that FXI and FXIa bind to FP with high affinity. Furthermore, FX activation downstream of FXIa cleavage of FIX is modulated by FP. These findings suggest a novel intercommunication between complement and coagulation pathways. Essentials Dysregulation of complement and coagulation go hand in hand and contribute to thromboinflammation. We explored crosstalk of complement factor properdin (FP) and intrinsic coagulation factor XI (FXI). FP is cleaved by activated FXI (FXIa), binds to FXIa with high affinity, and modulates FXIa activity. FP may modulate surface-driven FXIa activity with downstream functional consequences. 1 INTRODUCTION The complement and coagulation pathways play a central role in thromboinflammation. Both systems are descended from shared ancestry,1 and although the interactions between the two are yet to be completely defined, the two systems should not be considered as separate entities.2 Complement is a tightly regulated protease cascade and is a key player in host defense against microbial infection. This cascade can be activated by three pathways: the classical, lectin, and alternative pathways. These three pathways result in a common terminal pathway, culminating in membrane attack complex (MAC) formation.3 The classical and lectin pathways are inducible through conformational changes in the primary proteases through antibody-antigen complexes4 or when in contact with polysaccharides at microbial surfaces.5 The alternative pathway is different from the inducible classical and lectin pathways, constantly undergoing a process known as "tick-over," the spontaneous hydrolysis of the thioester bond of C3 creating C3(H2O), an analogue of C3b.6 C3(H2O) will either bind to pathogen surfaces to recruit further complement components or will remain soluble and be quickly degraded. Properdin (factor P [FP]) and factor B (FB) are recruited, forming a complex with surface bound C3(H2O), with FB binding in a Mg2+-dependent manner. FB is then activated by factor D, forming the initial C3 convertase. FP is a cofactor for the C3 convertase complex, increasing the half-life 10-fold,7 and is the only known positive regulator of complement, necessary for alternative pathway activation, and initiates a positive feedback loop, amplifying the terminal pathway and MAC generation culminating in lysis of pathogenic cells.8 FP is a highly positively charged 53-kDa monomer made of seven thrombospondin type-1 repeats. These monomers associate head to tail to create dimers, trimers, and tetramers in serum.9 FP circulates in the plasma at a concentration of 4 to 25 µg/mL and is constitutively released from a number of cells10 including monocytes,11 dendritic cells,12, 13 endothelial cells,10 mast cells,14 and adipocytes.15, 16 FP is also released from stimulated granulocytes, including neutrophils, in the local microenvironment, promoting complement activation; stimuli include tumor necrosis factor-α and C5a.17, 18 FP deficiency often displays a phenotype of recurring meningococcal infections, with higher mortality rates when compared to healthy individuals.19 The intrinsic pathway of coagulation is initiated through contact activation. Prekallikrein (PK) and factor XII (FXII) can undergo a reciprocal activation process enhanced by the presence of artificial and physiological negatively charges surfaces20 to generate kallikrein (PKa) and activated FXII (FXIIa). FXIIa generated from contact activation initiates the intrinsic pathway of coagulation through the cleavage of FXI to form FXIa. FXIa,21 along with PKa,22-25 can then cleave factor IX (FIX), subsequently leading to factor X (FX) activation, thrombin generation, and fibrin clot formation. It has been demonstrated that in the presence of surfaces such as sulfatides and glycosaminoglycans (GAGs), FXI also can autoactivate and induce coagulation.26 FXI is a zymogen that circulates at a concentration of 30 nM in the blood, most often in association with its cofactor, high-molecular-weight kininogen (HK).27 FXI is composed of two identical 80-kDa monomers linked by a disulfide bond. Each monomer contains four apple domains with similar structural properties to PK, which also circulates in complex with HK.28 Deficiency of FXI results in a mild to moderate bleeding disorder known as hemophilia C. FXI can be activated by FXIIa29, 30 and thrombin,31, 32 and FXIa has been shown to have numerous natural substrates including FIX, factor V, FX, prochemerin, and complement regulatory protein factor H (FH).33-35 Proteases from both the complement and contact activation systems have similar structural functions and characteristics, and it has been demonstrated that the classical pathway of the complement system can be initiated by FXIIa.36 Also, the common pathway of complement can be initiated through the cleavage of C3 by PKa.37 There is evidence that the lectin pathway of complement may interact with the kallikrein-kinin system through mannose-binding lectin-associated serine protease-1 cleavage of HK leading to bradykinin release.38 The primary inhibitor of the complement classical pathway, C1 esterase inhibitor (C1-INH) can also inhibit the intrinsic pathway of coagulation39 through inhibition of FXIIa, FXIa, and PKa,40 demonstrating how both systems are intricately related and have functional similarities. Polyanions including GAGs, polyphosphates, and phospholipids are key regulators of both complement and coagulation.41 They can induce contact activation of coagulation resulting in intrinsic activation, which can lead to initiation of the alternative pathway of complement. Some can also modulate inhibition of coagulation and complement via potentiating serpin activity.42 Phospholipids can mediate both complement and coagulation, and FXII can bind to apoptotic cells via phospholipid interactions,43 while the alternative pathway of complement can also activate upon binding to phospholipid surfaces.44 In this study, we have demonstrated for the first time that FXIa and FP have a direct interaction leading to functional consequences, revealing a novel intercommunication of the coagulation and complement pathways. These findings may have important implications in pathophysiological mechanisms involving intrinsic pathway and complement activation in thromboinflammatory conditions such as disseminated intravascular coagulation. 2 MATERIALS AND METHODS 2.1 Materials Human FP was sourced from Complement Technologies Inc. (Tyler, TX, USA) Human FXI, FIX, and FX zymogens and active enzyme FXIa (preactivated by FXIIa) were obtained from Haematologic Technologies Inc. (Essex Junction, VT, USA). Human single-chain HK was sourced from Enzyme Research Laboratories Ltd. (Llansamlet, UK). Dextran sulfate sodium salt from Leuconostoc sp. (500 kDa) was sourced from Sigma-Aldrich Corporation (Merck Group, St. Louis, MO, USA). Amine coupling reagents were obtained from GE Healthcare (Chicago, IL, USA). A Slide-a-Lyzer MINI dialysis device (MWCO 7000 Da was obtained from Life Technologies (Thermo Fisher, Waltham, MA, USA). Chromogenic substrates S-2288 and S-2765 were obtained from Quadratech Diagnostics Ltd. (East Sussex, UK). Four percent to 12% Bis-Tris Gels, 4× sample buffer, 10× LDS reducing buffer and 20× MES running buffer were all obtained from Thermo Fisher Life Technologies. Precision Plus Protein Dual Colour Standard was obtained from Bio-Rad Laboratories (Hercules, CA, USA). InstantBlue Protein Stain was obtained from Expedeon Ltd. (Cambridge, UK). All buffer ingredients were sourced from Sigma-Aldrich Corporation (Merck Group), unless otherwise stated. Phospholipids were obtained from Avanti Polar Lipids (Alabaster, AL, USA). 2.2 FXI chromogenic assay All chromogenic assays were performed using half-volume clear flat-bottom polystyrene 96-well plates (Fisher Scientific Ltd., Waltham, MA, USA) and 500 µM Chromogenix S-2288 chromogenic substrate with 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) buffered saline pH 7.4 with 1% (w/v) PEG8000 (HBS [10 mM HEPES, 150 mM NaCl]-P) unless otherwise stated. Cleavage of S-2288 was determined by absorbance changes of the reaction mixture as p-nitroaniline is released. All experiments were run in triplicate on one plate and were exported to Excel (Microsoft Corporation, Redmond, WA, USA). Readings were taken using a PowerWave HT Microplate Spectrophotometer (BioTek, Winooski, VT, USA) at 37°C at 405 nm every 12 seconds unless otherwise stated. 2.2.1 FXI autoactivation FP was titrated (5-25 µg/mL) in reactions of 30 nM FXI with 0.6 µg/mL dextran sulfate (DXS). The generation of FXIa formed was subsequently determined by monitoring cleavage of S-2288 every 12 seconds, over 120 minutes at 37°C. A similar assay was performed, replacing the titration of FP with a titration of protamine sulfate (0.78–50 µg/mL; Figure S1). 2.2.2 Michaelis-Menten kinetics Three nanoMolar of FXIa was incubated with and without 0.6 µg/mL DXS, in the presence and absence of 25 µg/mL FP using a twofold serial dilution of S-2288 (0.05-3.0 mM). FXIa catalytic activity was determined by monitoring cleavage of S-2288. 2.3 Substrate specificity assays Substrate specificity was analyzed using reducing SDS-PAGE. Incubations were performed and all samples were diluted twofold into a running buffer containing reducing agent, LDS sample buffer, and HBS. Samples were separated by reducing SDS-PAGE at 100 V for 52 minutes. The gel was stained with InstantBlue protein stain overnight at 21°C with gentle shaking, and washed three times with water with gentle shaking for 5 minutes. Gels were imaged using Syngene G:BOX Chemi and GeneSys software (Syngene, Bengaluru, India). 2.3.1 FXI in the presence of DXS and FP Reactions of 100 µg/mL FXIa and 200 µg/mL FP in the presence of 12.5 µg/mL DXS were incubated for 120 minutes in HBS and were diluted into the running buffer. Bands of interest were analyzed by liquid chromatography–mass spectrometry (LC-MS) (Appendix S1) by the Biomolecular Mass Spectrometry Facility at the University of Leeds. 2.3.2 FXIa substrate specificity Reactions of 100 µg/mL FXIa, 100 µg/mL FIX, and 200 µg/mL FP in the presence of 12.5 µg/mL DXS were incubated, and samples were taken over a course of 60 minutes and were diluted into the running buffer. 2.4 Binding of FXI and FP using surface plasmon resonance SPR was performed using the Pall/ForteBio Pioneer biosensor platform (Molecular Devices, LLC, San Jose, CA, USA) (Appendix S1). FP was immobilized to the sensor surface to around 1 × RMAX 79.55 RU using the amine coupling method as previously described.45 After priming three times, 50 nM of FXI or FXIa was injected over the sensor surface for the first experiment using a OneStep 100% loop inject, using Taylor dispersion to create a concentration gradient through the capillary tube before entering the flow cell (FC), at a flow rate of 30 µL/min with a dissociation time of 300 seconds. The sensor surface was regenerated using 5 µL of 1 M NaCl, 3 mM NaOH injected at 60 µL/min, with a dissociation time of 30 seconds. To determine the binding kinetics, a OneStep assay was performed. Response curves from FC2 were subtracted from FC1 and FC3. Buffer blanks were averaged and subtracted from the binding curves. The assay was run in triplicate, and the standard error of the mean was calculated using Prism 8 (GraphPad Software, San Diego, CA). 2.5 FXIa downstream activity chromogenic assay 2.5.1 Phospholipid vesicle preparation Phospholipids were prepared as previously described.46 Micelles were formed from phospholipids supplied in chloroform, using 20% (v/v) di-oleic phosphatidylethanolamine, 20% (v/v) di-oleic phosphatidylserine, and 60% (v/v) di-oleic phosphatidylcholine dehydrated and resuspended in HBS. Reactions of 125 pM FXIa, 100 nM FIX, 300 nM FX, 125 pM HK, 100 µM phospholipids, and 25 µg/mL FP were analyzed using a chromogenic assay to determine FX activation downstream of FXIa activation of FIX. FX activation was measured by monitoring cleavage of 700 µM chromogenic substrate S-2765 at 37°C at 405 nm every 12 seconds for 360 minutes. Maximum rates of reactions were calculated from the first derivatives of each assay condition. 2.6 Data analysis and statistics All data figures were created using GraphPad Prism 8 unless otherwise stated. 2.6.1 Statistical analysis All analysis was performed in GraphPad Prism 8 unless otherwise stated. Statistical differences were analyzed by one-way analysis of variance (anova), and tests are highlighted in figure legends where appropriate. 2.6.2 Surface plasmon resonance KD was calculated using Qdat data analysis software package (Pall FortéBio, Menlo Park, CA, USA), specific for Molecular Devices Pioneer data sets. 3 RESULTS 3.1 Amidolytic activity of FXI autoactivated by DXS is modulated in the presence of FP This study was initiated by investigating the effect of FP on FXI autoactivation by the synthetic GAG DXS. In a purified system, physiological concentrations of FP and FXI were incubated in the presence and absence of DXS for 90 minutes. The presence of DXS rapidly induced amidolytic activity of FXI toward S-2288 via autoactivation to FXIa (Figure 1A). The addition of FP (5–25 µg/mL) to the autoactivation reaction drastically reduced cleavage of S-2288 in a dose-dependent manner (Figure 1B). To determine if this effect was due to the cationicity of FP, the same experiment was repeated using a titration of the cationic protein protamine sulfate, a clinical reagent applied for the reversal of heparin anticoagulation.47 It was observed that protamine sulfate reduced the cleavage of chromogenic substrate by FXI autoactivation in the presence of DXS, though this was not dose dependent with the employed concentrations (Figure S1). To determine if the decreased cleavage of the chromogenic substrate was due to a change in substrate specificity, reactions of FXI, DXS, and FP were incubated for 120 minutes and were analyzed using reducing SDS-PAGE. Novel cleavage bands were revealed and were analyzed by LC-MS (Table S1). The cleavage products were found to be FP, suggesting a change in substrate specificity of FXIa away from the chromogenic substrate and toward FP. Similar reactions were performed and analyzed using SDS-PAGE; however, FXI was replaced with its activated form, purified FXIa (preactivated by FXIIa) (Figure 1D). The cleavage products of FP were still visible, suggesting that FP can be cleaved by FXIa autoactivated by DXS, or by FXIa activated by FXIIa. These data suggest a surface-dependent interaction between FXI and FP. FIGURE 1Open in figure viewerPowerPoint FP acts as a substrate for FXIa in the presence of DXS. A chromogenic assay was employed to determine the effect of FP on the autoactivation of 30 nM FXI by 0.6 μg/mL DXS. FXI autoactivation was measured by cleavage of 500 μM chromogenic substrate S-2288 over 90 minutes. (A) Controls: FXI only (blue), DXS only (purple), FP only (red), FXI + DXS (maroon), FP + FXI (no DXS, green), FP + DXS (no FXI, orange). (B) FXI autoactivation by DXS in the presence of a titration of physiological concentrations of FP (5–25 μg/mL). The maximum rate of reaction calculated using the first derivative. Optical density was read at 405 nm, at 12 second intervals at 37°C. Data are expressed as median ±interquartile range, constructed of one experiment run in triplicate. (C) SDS-PAGE reveals a substrate specificity change of FXIa toward FP. (D) Purified FXIa can cleave FP in the presence of DXS. Bands A, B, C, and D were analyzed by mass spectrometry and were revealed to be FP (Table S1). Abbreviations: DXS, dextran sulfate; FP, factor P; FXI, factor XI; FXIa, activated factor XI 3.2 FXIa is still able to cleave its natural substrate, FIX, in the presence of FP and DXS It was important to investigate the effect of FP on cleavage of FIX by FXIa in the presence of DXS to elucidate whether the changes in substrate specificity may implicate the activation of coagulation via the intrinsic pathway. Reactions of FXIa, FIX, FP, and DXS were incubated as a time course, for up to 60 minutes. The samples were analyzed using reducing SDS-PAGE. It was indicated that FXIa was able to cleave both FIX and FP in the presence of DXS (Figure 2). FIGURE 2Open in figure viewerPowerPoint FXIa can cleave its physiological substrate, FIX, and FP in the presence of DXS. Reactions of 100 μg/mL FIX, 100 μg/mL FXIa, 200 μg/mL FP, and 12.5 μg/mL DXS were incubated at 37°C for up to 60 minutes with samples taken intermittently after briefly mixing with a vortex. Reducing SDS-PAGE was performed to analyze FXIa substrate specificity. Activation of FIX was determined by the appearance of the FIXa light chain, cleavage of FP was determined by the appearance of the heaviest cleavage product at around 40 kDa. Abbreviations: DXS, dextran sulfate; FIX, factor IX; FIXa, activated factor IX; FP, factor P; FXI, factor XI; FXIa, activated factor XI 3.3 DXS modulates the kinetics of FXIa, but this is further modified in the presence of FP Subsequently, we explored FXIa activity in the presence and absence of DXS and FP (Table 1). The data were analyzed using the kcat model in GraphPad Prism. DXS alone reduced the turnover rate of S-2288, demonstrated by the decrease in maximum velocity (Vmax) of FXIa toward the substrate from 6.3 × 10−7 to 1.6 × 10−7 (M.s−1). This reduced turnover rate observed at concentrations above the Km is due to a significant reduction in kcat from 209.5 to 51.8 s−1, which was also compensated for by a significant decrease in Km 4.9×10−4 to 3.3×10−5 M. The decrease in both kcat and Km leads to an overall increase in kcat/Km. The addition of FP alone did not modulate FXIa activity; however, it reversed the reduction of kcat by DXS from 51.76 to 88.4 s−1 and partially reversed the decrease in Km from 2.1×10−4 M to 3.3×10−5. These data suggest that FP is most likely interfering with the interaction between FXIa and the polyanionic surface presented by DXS; however, the partial reversal of the reducing effect on Km supports a potential substrate specificity change of FXIa. TABLE 1. FP reduces the inhibitory effect of DXS on FXIa catalytic activity kcat ± SEM (s−1) Km ± SEM (M) Vmax (M.s−1) kcat/Km (s−1 M−1) FXIa 209.5 ± 3.8 4.9 × 10−4 ± 2.6 × 10−5 6.3 × 10−7 4.24 × 105 FXIa + FP 196.1 ± 5.6 4.3 × 10−4 ± 3.7 × 10−5 5.9 × 10−7 4.61 × 105 FXIa + DXS 51.8 ± 4.3 3.3 × 10−5 ± 1.5 × 10−5 1.6 × 10−7 1.59 × 106 FXIa + FP + DXS 88.4 ± 6.9 2.1 × 10−4 ± 5.9 × 10−4 2.7 × 10−7 4.14 × 105 Note Michaelis-Menten kinetic analysis was performed to determine how FP affected FXIa catalytic activity in the presence and absence of DXS. Reactions of 25 µg/mL FP and 3 nM FXIa were incubated ±0.6 µg/mL DXS with a twofold titration of S-2288 (0.05–3 mM). FXIa catalytic activity was measured by cleavage of S-2288 over 3 h. Optical density was read at 405 nm, at 12-s intervals at 37°C. Kinetic analysis was performed using the kcat model on GraphPad Prism. Catalytic activity defined by amount of pNA released per second (M.s−1). Data represented as mean ± SEM constructed of one experiment run in triplicate. Abbreviations: DXS, dextran sulfate; FP, factor P; FXIa, activated factor XI; kcat, first-order rate constant; Km, Michaelis constant; pNA, p-nitroaniline; SEM, standard error of the mean. 3.4 FXI and FXIa bind to FP with high affinity Binding studies were performed using SPR to determine if there was a direct interaction between FXIa and FP. FP was immobilized to the sensor surface and FXI and FXIa were titrated over the surface using the OneStep protocol, with a maximum concentration of 50 nM. We found that both FXI and FXIa bind to FP with a KD (equilibrium dissociation constant) of 16.1 nM and 350 pM, respectively (Figure 3A, B). These data suggest that FP can bind to both activated and zymogen FXI but with a preference to the active enzyme due to a higher-affinity interaction. FIGURE 3Open in figure viewerPowerPoint FXI and FXIa bind to FP with high affinity. Kinetic analyses were performed by SPR with human FP immobilized to the sensor surface to 79.55 RU. (A) 50 nM FXI was injected and bound to FP with a KD of 16.1 nM. (B) 50 nM FXIa was injected and bound to FP with a KD of 350 pM. Data are expressed as mean ± SEM constructed of one experiment run in triplicate. Abbreviations: FP, factor P; FXI, factor XI; FXIa, activated factor XI; KD, equilibrium dissociation constant; SPR, surface plasmon resonance 3.5 FP modulates FX generation by the intrinsic pathway in purified reactions The purpose of this experiment was to measure FXIa activation of FIX; however, due to the low catalytic activity of FIXa toward chromogenic substrates, this was performed indirectly by observing FX activation by FIXa. The FX concentration (300 nM) is at the concentration of the Km of FIXa toward FX, and the concentration of the chromogenic substrate S-2765 (700 µM) is at the Vmax of FXa; FX cleaving the substrate is not the rate-limiting factor. The rate-limiting factors of this assay would therefore be FXIa activation of FIX, or FIXa activation of FX. The effect of FP on the resulting activation of FX by FIXa was explored, in the presence and absence of HK and phospholipids. In the absence of phospholipids (Figure 4A), HK appeared to have little effect on the cleavage of S-2765 in the absence of FP. However, in reactions including FP with HK, the cleavage of S-2765 was significantly reduced when compared to all other assay conditions without phospholipids (P ≤ .05). The addition of 100 µM of phospholipids enhances FXa generation in all conditions (Figure 4B); however, there is a similar trend where FP reduces the cleavage of the chromogenic substrate in the presence and absence of HK (P ≤ .05). FIGURE 4Open in figure viewerPowerPoint FP modulates downstream effects of FXIa by leading to reduced cleavage of chromogenic substrate S-2765 by FXa. Reactions of 125 pM FXIa, 100 nM FIX, 300 nM FX, 125 pM HK, 100 μM PL, and 25 μg/mL FP were analyzed using a chromogenic assay to determine FX activation downstream of FXIa activation of FIX. FXa catalytic activity was measur
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