A Bipartite Autoinhibitory Region within the B-domain Suppresses Function in Factor V*

Background: Factor V is an inactive procofactor. Removal of its B-domain drives activation through an undefined mechanism. Results: Basic and acidic regions within the B-domain impair factor Xa binding and cofactor function. Conclusion: Autoinhibitory B-domain segments maintain the procofactor state and their disruption activates FV. Significance: The study provides insights into how FV activation unfolds and defines an unexpected sequence-specific function of the B-domain. Activation of blood coagulation factor V (FV) is a key reaction of hemostasis. FV circulates in plasma as an inactive procofactor, and proteolytic removal of a large central B-domain converts it to an active cofactor (FVa) for factor Xa (FXa). Here we show that two short evolutionary conserved segments of the B-domain, together termed the procofactor regulatory region, serve an essential autoinhibitory function. This newly identified motif consists of a basic (963–1008) and an acidic (1493–1537) region and defines the minimal sequence requirements to maintain FV as a procofactor. Our data suggest that dismantling this autoinhibitory region via deletion or proteolysis is the driving force to unveil a high affinity binding site(s) for FXa. These findings document an unexpected sequence-specific role for the B-domain by negatively regulating FV function and preventing activity of the procofactor. These new mechanistic insights point to new ways in which the FV procofactor to cofactor transition could be modulated to alter hemostasis.

Complex reaction pathways, including blood clotting, often rely on regulated protein activation to elicit a biologic response. Coagulation factors generally circulate in blood as inactive precursors and transition to an active form after limited proteolysis subsequent to vascular damage. For serine protease zymogens involved in clotting, this mechanism is well described (1). Although precise cleavage sites are defined, the mechanism underpinning the conversion of FV to its active form (FVa) 3 has remained elusive. FV plays a pivotal role in blood coagulation. It is a large, heavily glycosylated, inactive procofactor protein that is homologous to factor VIII (FVIII) and shares the same domain organization (A1-A2-B-A3-C1-C2) (2,3). FV cannot participate to any significant degree in the macromolecular enzyme complex prothrombinase. It is converted to the active cofactor state after limited proteolysis within the B-domain. FVa is a nonenzymatic cofactor within the prothrombinase complex that greatly accelerates the ability of factor Xa (FXa) to rapidly convert prothrombin to thrombin (4). FV activation has been studied for more than three decades, yet how bond cleavage within the B-domain facilitates the conversion from an inactive to active state is only starting to become known.
The FV B-domain spans amino acids 710 -1545 and is not necessary for procoagulant activity ( Fig. 1) (5)(6)(7)(8). Thrombin, utilizing both exosites I and II, is considered a key physiologic activator and cleaves three peptide bonds (Arg 709 , Arg 1018 , and Arg 1545 ) to generate FVa (5-7, 9 -14). Prior studies of FV activation were largely based on correlating bond cleavage with the development of procoagulant activity (for review, see Ref. 3). Broadly, these studies found that variable amounts of cofactor activity are observed depending on which region of the B-domain is cleaved and which assay is used to evaluate activity. A clear consensus is that maximal activity correlates with cleavage at Arg 1545 (7,13,(15)(16)(17)(18)(19)(20)(21)(22). Although these studies have advanced the field, such correlative studies have not provided mechanistic insight into how FV activation unfolds.
The human FV B-domain (836 residues) is generally not well conserved among vertebrates, varies in size across species, and has no homology to any other known protein, including the FVIII B-domain (3,9,23). A longstanding assumption is that the B-domain, due to its size/high carbohydrate content, nonspecifically prevents activity of the procofactor. Initial evidence for this came from the Kane laboratory (17,24), who generated a FV derivative with a shortened B-domain (FVdes 811-1491 or FV-810). Using a transient expression system, they found that this FV derivative had partial but seemingly constitutive activity (17). Our laboratory, using purified FV-810 and a thrombin cleavage site variant, found that FV-810 functions in an identical way to FVa (25). These data imply that proteolysis within the B-domain, although necessary, is incidental to the mechanism by which cofactor function is realized. Instead, activation of FV must eliminate steric and/or conformational constraints contributed by the B-domain. Surprisingly, using a panel of B-domain-truncated variants, we found that specific B-domain sequences appear to play a critical role in stabilizing FV in an inactive procofactor state (26). One of these regions (963-1008) is unusually basic and is one of just a few sections of the B-domain that is conserved across the vertebrate lineage (3). Disruption of these sequences (termed here the basic region (BR)) by mutagenesis or deletion yielded derivatives with cofactor-like properties in the absence of proteolysis (26).
Here we expand on these findings and show that although the BR is necessary, it is not sufficient to suppress cofactor function.
Rather, it appears to work in concert with sequences at the C-terminal end of the B-domain (1493-1537, Fig. 1). This region, termed here the acidic region (AR), is similar to the a3 region of FVIII and, like the BR, is conserved across species. Overall the data support the novel idea that these discrete sequences (BRϩAR), together defined as the procofactor regulatory region (PRR), are the minimal, autoinhibitory elements required to maintain FV as an inactive procofactor.
Construction of rFV Variants-Construction of FV-810 and FV-1033 has previously been described (25,26). Specific oligonucleotides used to generate FV-B226 were as follows: forward primer A, 5Ј-GAAGAGGTGGGAATACTTC-3Ј, encoding for amino acid residues 320 -325; reverse primer B, 5Ј-GTGGCC-ACTCTGCTTTCCAGGATCCTCTATAGGGTCTTCAG-3Ј, in which the first 21 bases correspond to full-length FV cDNA, encoding for residues 964 -970 and the last 19 bases to residues 805-810; forward primer C, 5Ј-CTGAAGACCCTATAGAG-GATCCTGGAAAGCAGAGTGGCCAC-3Ј, in which the first 19 bases correspond to residues 805-810 and the last 21 bases correspond to full-length FV cDNA residues 964 -970; reverse primer D, 5Ј-TCTGTCCATGATAAGAAATGG-3Ј, corresponding to the full-length FV cDNA sequence encoding for residues 1871-1877. The resulting DNA fragment was TOPOcloned (Invitrogen), digested with Bsu36I and SnaBI, gel-purified, and subcloned into pED-FV digested with the same enzymes (25). To ensure the absence of polymerase-induced errors, the entire modified cDNA was sequenced. The remaining FV constructs outlined in the manuscript were prepared in the same type of way using appropriately modified primers. The FV cDNA sequence of Gallus gallus (chicken) was derived from the Ensembl genome data base (Version 35). The base pairs encoding the chicken B-domain were synthesized (GenScript) and flanked by HpaI and SnaBI restriction sites to facilitate cloning.
Expression and Purification of rFV-Transfection of the plasmids encoding FV constructs into baby hamster kidney cells, selection of stable clones, and expression/purification of rFV derivatives were performed as described (25,33). Protein purity was assessed by SDS-PAGE using precast 4 -12% gradient gels (Invitrogen) under reducing conditions (50 mM dithiothreitol) using the MOPS buffer system followed by staining with Coomassie Brilliant Blue R-250.
FV-specific Prothrombin Time (PT)-based Clotting Assay-FV (600 nM) derivatives were prepared in assay buffer. For experiments in which pretreatment with thrombin was intended, FV derivatives were incubated at 37°C for 15 min with 10 -60 nM thrombin. All thrombin-dependent activation reactions were quenched by the addition of a 1.2-fold molar excess of hirudin. Samples were diluted to less than 3 nM in assay buffer with 0.1% BSA, and the specific clotting activity using FV-deficient plasma (George King Biomedical, Overland Park, KS) and TriniClot PT Excel (Tcoag, Wicklow, Ireland) was assayed as described (21). The data are presented as the mean values Ϯ S.D.
Prothrombin Activation-Steady state initial velocities of prothrombin cleavage were determined discontinuously at 25°C as described (32). Progress curves of prothrombin activation were performed using the following reaction conditions. PCPS (50 M), DAPA (3 M), and prothrombin (1.4 M) were incubated with the various rFV(a) derivatives (0.1 nM) in assay buffer, and the reaction was initiated with FXa (1.0 nM). At various time points, aliquots of the reaction mixture were quenched, and thrombin generation was determined using the chromogenic substrate S2238 as described (32).
Fluorescence Measurements-Steady state fluorescence intensity and/or anisotropy was measured at 25°C in a PTI QuantaMaster fluorescence spectrophotometer (Photon Technology International) using ex ϭ 480 nm and em ϭ 520 nm with long pass filters (KV500, CVI Melles Griot) in the emission beam. Reaction mixtures (2.5 ml) in a 1 ϫ 1-cm 2 quartz cuvette contained 20 or 30 nM OG 488 -FXa and 50 M PCPS in assay buffer to which increasing concentrations of FV/V(a) derivative (0.5-100 nM) were added. Fluorescence anisotropy or intensity measurements, including controls, were performed as described (29,34).
Data Analysis-Data were analyzed according to the indicated equations by nonlinear least squares regression analysis using the Marquardt Algorithm (35), and the quality of each fit was assessed by the criteria described (36). Dissociation constants (K d ), stoichiometries (n), and the maximum increase in anisotropy at saturating rFV were obtained for the membranedependent interaction between FXa and rFV from the dependence of the anisotropy with increasing concentrations of rFV(a), which was corrected for the overall change in fluorescence intensity (37,38).

Role of the BR in Preserving the Procofactor State-
We have previously shown that removal of FV-B-domain residues 902-1033 and more specifically 963-1008, termed here the basic region or BR, drives the expression of FVa procoagulant function (26). The BR appears to stabilize the inactive FV procofactor state through a mechanism that is not well understood. To examine if the BR is sufficient to keep FV inactive, we produced a new panel of recombinant FV variants. Using a constitutively active FV derivative, FV-810 (residues 811-1491 deleted), as a scaffold (25), different extensions of the BR were inserted after residue 811, and the functional properties of the new variants (FV-B226, FV-B208, and FV-B199) were evaluated. Because these new FV variants are very similar, only FV-B199 is shown in Fig. 1. These variants have residues 964 -1033 (FV-B226), 964 -1015 (FV-B208), and 964 -1007 (FV-B199) added back to FV-810. Each variant migrated on SDS-PAGE with the expected mobility either before or after treatment with thrombin (Fig. 2).
Consistent with previous studies (25,26), FV-810-like FVa exhibits high specific activity before or after treatment with thrombin in a one-stage PT-based clotting assay using FV-deficient plasma ( Fig. 3A and Table 1). In contrast, FV-B226, FV-B208, or FV-B199 with variable BRs inserted reduced the specific activity to a level comparable with PD-FV. Treatment of these procofactor-like derivatives or PD-FV with thrombin resulted in a substantial increase in specific activity, with levels comparable with FV-810 ( Fig. 3A and Table 1). Additionally, progress curves of prothrombin conversion to thrombin using FXa-FV(a) yielded results consistent with the clotting assay. Unlike FV-810, the procofactor-like derivatives and PD-FV had very little activity and displayed progress curves of thrombin generation characterized by a substantial lag (Fig. 3B). Conver- sion of the FV variants to FVa by thrombin resulted in maximal cofactor activity and yielded rates of prothrombin activation comparable with FV-810 and FVa (Fig. 3C).
Although activity measurements are informative, they can be misleading, as feedback reactions during the assay could compromise data interpretation. To address this, we evaluated the ability of each of the FV variants to bind membrane-bound FXa using fluorescence measurements. Consistent with previous observations (25,26), FVa and FV-810 bound with high affinity to active site-blocked, membrane-bound FXa (Fig. 4, A and B, Table 1). In contrast, the interaction of FV-B226, FV-B208, FV-B199, or PD-FV with membrane bound-FXa was dramatically reduced compared with FV-810 as no saturable binding was observed (Fig. 4A, Table 1). Binding parameters for these proteins could not accurately be assessed; however, a lower limit estimate of the affinities indicates that they are at least Ͼ50-fold reduced compared with FV-810. Treatment of FV-B226, FV-B208, or FV-B199 with thrombin followed by assessment of direct binding yielded dissociation constants similar to thrombin-treated FV-810 and FVa (Fig. 4B), indicating that once activated each of the variants can assemble within prothrombinase. The binding data and functional measurements demonstrate that the BR is a necessary segment of the B-domain and plays a crucial role in keeping FV in an inactive, procofactor-like state. It appears to do so by obscuring FXa binding either directly or allosterically despite Ͼ75% of the B-domain being absent. Remarkably, the insertion of as little as 44 BR residues (e.g. FV-B199) had a major influence on FXa binding, shifting the functional status from cofactor-like to procofactor-like.
Contribution of Additional B-domain Sequences to Maintaining FV as a Procofactor-The findings suggest that a small B-domain harboring the BR (e.g. FV-B199) contains the necessary structural features to maintain the FV procofactor state. However, residual B-domain sequences apart from the BR could also play an important stabilizing role. Using FV-B199 as a scaffold, we removed sequences on either the C-terminal side (residues 1492-1538; FV-B152) or N-terminal side (residues 716 -810; FV-B104) of the B-domain (see Fig. 1). Residues flanking Arg 709 and Arg 1545 were left intact to retain efficient  processing by thrombin. FV-B152 or FV-B104 migrated on SDS-PAGE as expected and were cleaved by thrombin to yield FVa (Fig. 2).
Elimination of ϳ100 residues (716 -810) from FV-B199 on the N-terminal side of the B-domain (FV-B104; see Fig. 1) was without functional consequence as FV-B104 remained a procofactor as assessed by clotting, purified component assays, and direct binding measurements to FXa (Fig. 3, A and B, supplemental Fig. S1 and Table 1). After treatment with thrombin, FV-B104 exhibited functional properties similar to FV-810 (Fig.  3, A and C). In contrast, removing sequences C-terminal to the BR (residues 1492-1538; FV-B152, see Fig. 1) converted an otherwise inactive FV derivative (e.g. FV-B199) to an active cofactor even in the presence of the BR. The overall activity of FV-B152 was similar to FV-810, and it bound FXa with high affinity (Fig. 3, A-C, supplemental Fig. S1 and Table 1). These findings indicate that in addition to the BR, C-terminal B-domain sequences 1493-1537 also contribute to stabilizing FV in an inactive procofactor state. Inspection of this region of the B-domain reveals that 1493-1537 is highly acidic (termed herein the acidic region), is generally conserved across the vertebrate lineage (see supplemental Fig. S2), and is similar to the a3 region of FVIII at the beginning of its light chain. Overall, these data suggest that the BR works in concert with the AR to suppress cofactor function. Thus the BR and AR, consisting of ϳ100 residues and together defined here as the procofactor regulatory region, are the minimal, autoinhibitory elements required to maintain FV as a procofactor. Elimination of either the BR (e.g. FV-810) or AR (e.g. FV-B152) removes critical structural motifs that otherwise keep FV functionally inert. Furthermore, the juxtaposition in the primary sequence of the BR and AR in FV-B199 and FV-B104 (see Fig. 1) suggest that these segments act as independent motifs and do not appear to be influenced in a major way by the rest of the B-domain.
Specificity of the BR and Fine Mapping-Considering the functional importance of the PRR, it is not surprising that most, if not all, of available FV sequences across the vertebrate lineage have a conserved BR and AR, albeit with weaker conservation in lower vertebrates (see supplemental Fig. S2). An exception to this is FV derived from the venom of certain Australian snakes (39 -41). Venom FV from Pseudonaja textilis (ptex-FV) has a B-domain of just 46 residues that lacks the BR but contains a region similar to AR. Consistent with the importance of an intact PRR in keeping FV inactive, we have shown that ptex-FV is constitutively active and does not require processing/removal of its B-domain (42,43).
To test specificity and functionality, we examined whether B-domains from select vertebrates, which have divergent PRRs, preserve the human FV procofactor state. As expected, exchanging only the human FV B-domain (836 residues) with that of ptex-FV (46 residues, no BR; FV-B-Ptex) yielded a FV derivative that was constitutively active, as determined by clotting assay, and it exhibited high affinity binding to FXa ( Table 1   and supplemental Fig. S3). Surprisingly, however, B-domains from lower vertebrates, which harbor a PRR, did not suppress cofactor activity. For example, a human FV derivative harboring only the chicken B-domain (FV-B-Ch) or pufferfish B-domain (FV-B-Fish) displayed a high specific clotting activity and high affinity FXa binding in the absence of thrombin activation (Table 1 and supplemental Figs. S3 and S4). These data imply that the mechanism for maintaining the procofactor state of FV in lower vertebrates is fundamentally different, or alternatively, a high level of specificity mediates the autoinhibitory function of the PRR. Lending some support to the latter, when we placed only 44 residues of the human BR within the chicken B-domain (FV-B-Ch ϩhBR ), the procofactor state was reestablished (supplemental Figs. S3 and S4). This procofactor-like species could be fully processed and activated by thrombin to FVa (supplemental Fig. S4). These data suggest that either other factors may serve to inhibit the function of FV in these lower vertebrates or that the mode of inhibition of the PRR is highly specific and a major contributor to this specificity is the BR.
We next mapped the human BR further to define the extent to which specific portions stabilize FV. Using a previously described procofactor-like variant (FV-1033, Fig. 5A) as a scaffold (26), short segments of the BR were retained, and the remaining sequence was replaced with unrelated FVIII B-domain sequence. Three variants were expressed and purified (FV-B8-BR1, FV-B8-BR2, and FV-B8-BR3; Fig. 5B), and they are schematically shown in Fig. 5A with the original FV BR residues highlighted in blue and FVIII B-domain residues shown in green. This approach allowed us to focus on the individual role of stretches of 10 -12 BR residues.
Previous analysis of a FV variant in which the entire basic sequence was exchanged for FVIII B-domain residues (FV-B8 -46) demonstrated that this derivative has cofactor-like properties similar to FV-810 (26). Assessment of the specific clotting activities of the newly generated FV-B8-BR variants revealed a gradual decline in cofactor activity depending on which BR sequence was preserved. Maintaining residues 971-980 (BR1), while exchanging the rest of the BR for FVIII B-domain sequence resulted in a cofactor-like FV variant (FV-B8-BR1; Fig. 6A). However, preserving the second (BR2; residues 983-994) or third (BR3; residues 997-1008) subset of the BR reduced the specific activity, thereby generating an intermediate (FV-B8-BR2) or more procofactor-like FV variant (FV-B8-BR3). These findings were confirmed in a purified system where we monitored the conversion of prothrombin to thrombin (Fig.  6B). Upon treatment with thrombin, the FV variants displayed a high specific activity by clotting assay (Fig. 6A). Furthermore, in the purified component assay, FV-B8-BR3 displayed a high level of activity, whereas there was only a very modest change in activity of FV-B8-BR2 after thrombin treatment (Fig. 6C). Based on these observations, we conclude that the C-terminal portion (residues 997-1008) of the BR has the most influence in suppressing cofactor function, thereby maintaining the procofactor state.

DISCUSSION
It has been recognized for more than 30 years that the large central B-domain of FV is responsible for the lack of activity in the precursor (3). Due to its size/high carbohydrate content, it has been generally assumed that the B-domain nonspecifically prevents activity of the procofactor. Here we show that the B-domain harbors an autoinhibitory motif that is essential for the regulation of FV function. Termed the procofactor regulatory region, the motif consists of two evolutionary conserved segments of the B-domain, one which is highly basic (BR) and one that has a concentration of ARs. These regions work together to obscure a high affinity binding site for FXa. The unraveling of the autoinhibitory PRR via B-domain proteolysis is the central driving force converting the inactive procofactor (FV) to the active cofactor state (FVa).
Keeping FV as an inactive procofactor undoubtedly plays a critical regulatory role rooted in the tight regulation of thrombin generation. Having a potent regulatory motif such as the PRR that provides "on-site" repression of cofactor activity is thus of central importance for maintaining normal hemostasis. Due to its significance, it is not surprising that the ϳ100 amino acids that make up the PRR are generally conserved across vertebrate evolution (supplemental Fig. S2) even though there is weak homology among B-domains from mammals (Ͻ50% sequence identity) and lower vertebrates (Ͻ20%) (3,44). Surprisingly, even the length of the B-domain varies across the vertebrate lineage, from 836 residues in humans to 471 in pufferfish. However, common threads of these B-domains include high carbohydrate content, large size, and the presence of the PRR. Results of the current study suggest that the large size of the B-domain likely has little, if any, impact in keeping FV inactive. For example, we found that Ͼ85% of the B-domain is dispensable with respect to the inhibition of FV cofactor activity. Functional measurements revealed that FV-B104, consisting of just 104 amino acids and essentially only harbors the PRR, is a procofactor. Although further work would need to be done, it is possible that other factors apart from the PRR especially in lower vertebrates may serve to inhibit the function of FV.
Within the PRR, both the BR and AR play critical roles in keeping FV inactive as elimination of either shifts the functional status to the cofactor-like state. The BR and AR are separated in the primary sequence of human FV by ϳ480 amino acids. Interestingly, approximately half of this region has 31 copies of 9amino acid tandem repeats (9,45,46). However, lower vertebrates such as lizard, chicken, and pufferfish do not have any repeat segments, and the length separating the BR and AR is very short at Ͻ55 residues in these species. In this study we essentially recapitulated this type of orientation with human FV as juxtaposition of the BR and AR (e.g. FV-B199 and FV-B104, see Fig. 1) had no effect on PRR function. This suggests that the BR and AR are likely specialized motifs that function together independent of the vast majority of the B-domain. Interestingly, the region separating the BR and AR has increased in size during the course of evolution; however, this part of the B-domain has no known function. This region in mammals is heavily glycosylated and could play a role in intracellular trafficking or influence the circulating half-life of FV (47,48).
We speculate that the PRR functions as an autoinhibitory motif within the large B-domain and is a modular effector of cofactor function. Throughout biology, a prevalent mechanism employed for negatively regulating otherwise constitutively active proteins is the incorporation of cis-acting inhibitory sequences (49,50). A hallmark of this autoinhibition mechanism is the identification of the protein fragment(s) that inhibits or represses the mature, active protein. For FV, our data support the idea that the PRR solely serves this function (see Fig. 7). The autoinhibitory effect of the PRR could be mediated by direct masking of a functional region or could occur by an indirect/allosteric mechanism. In either scenario, the underpinnings of this inhibition likely derive from altering the interaction with FXa. Notably, FXa binding is significantly inhibited or essentially undetectable in all FV derivatives that harbor an intact PRR. The FXa binding site is thought to reside on the A2 domain with contributions from the A3. Largely driven by mutagenesis studies, it appears that several key residues in the A2 contribute in a major way to the binding energy (51). This is consistent with reports suggesting that a region surrounding the activated protein C cleavage site at Arg 506 is involved in FXa binding (52)(53)(54). In principle, relief of the autoinhibitory interaction could occur by several mechanisms; however for FV, proteolysis within the B-domain is the driving force. Cleavage at Arg 709 , Arg 1018 , and Arg 1545 ultimately dismantles the PRR consequently exposing the FXa binding site (Fig. 7). At present, it is not clear which of the individual cleavage sites has the most impact on destabilizing the PRR. However, cleavage at Arg 1545 , which is adjacent to the AR, must have a significant impact. Support for this comes from the longstanding observation in the field that cleavage of FV by a protease in Russell's viper venom at Arg 1545 results in full activation (7,13,(15)(16)(17)(18)(19)(20).
Due to the nature of how the PRR inhibits cofactor function, it is likely that there are multiple ways in which FV could be activated. As long as the PRR is sufficiently disrupted or disengaged from the core heavy/light region, the protein should bind FXa and function in prothrombinase. Clear examples of this from our work are FV-810 (lacks AR) and FV-B152 (lacks BR), which have altered PRRs and are constitutively active. Furthermore, numerous proteases have been identified that process FV to varying functional states in a manner different from thrombin (for review, see Ref. 3). The use of sequence-specific B-domain regions to suppress cofactor activity is in stark contrast to the mechanism underlying FVIII activation. For example, B-domainless FVIII remains a procofactor, and processing between the A1 and A2 domain at Arg 372 is absolutely required for the development of FVIIIa activity (3,23). Furthermore, FVIII association with von Willebrand factor also contributes to maintaining the procofactor state as it obscures functional membrane binding sites (55). The clear differences in the mechanism by which FVIII and FV are kept inactive are also evident from naturally occurring mutations. For FVIII, missense mutations have been identified (e.g. Arg 372 and Arg 1689 ) that alter the rate and/or extent of FVIII activation and cause hemophilia A. Although FV deficiency is rarer, there are no known missense mutations for FV that alter its activation (56). We speculate that because there are multiple routes to disrupt the PRR, a single amino acid change would unlikely be so unfavorable as to substantially impact FV activation. The observation that FV and FVIII employ differential mechanisms to maintain the procofactor state is surprising considering the clear evolutionary link between the two proteins (57,58). However, it is possible that there were different selective pressures on FV and FVIII that necessitated a diverse and/or stringent mechanism of control of cofactor activity development. The observation that FVIII must be cleaved at very specific sites and dissociate from von Willebrand factor (unlike FV) to express activity suggests that this could be the case (59).
The ability of the PRR to regulate the FV procofactor to cofactor transition through an autoinhibitory mechanism provides an unexpected twist to the problem of FV activation. Structural information would provide much needed insight into how the PRR maintains FV as an inactive procofactor. However, apart from electron microscope images of FV that show the B-domain as an appendage stemming from a globular core, presumed to be the heavy/light chain (60 -65), there is no structural information. Although the structure of inactivated bovine FVa lacking the A2 domain is available, little can be gleaned in terms of FV activation (66). Due to its large size and high carbohydrate content, detailed structural information of the FV B-domain may not be possible. However, information obtained in this study identifying the PRR as the core functional unit of the B-domain possibly makes structural studies of this region within grasp. High resolution structural information may reveal whether the PRR is keeping FV inactive directly or allosterically. This information may also shed light on where FXa engages the heavy/light chain region, as the PRR appears to obscure its binding. Furthermore, this information could also be used to develop therapeutic probes that target the autoinhibitory PRR or even mimic the PRR to suppress cofactor function. The identification of the sequence-specific function of the PRR makes the development of these types of stabilizing or destabilizing probes to modulate FV/FVa function possible.
In summary, work in this study unexpectedly shows that there are well conserved, discrete segments of the FV B-domain, termed the procofactor regulatory region, that serves an essential autoinhibitory function. The PRR is a cis-acting motif that through a direct or allosteric mechanism plays a key role in keeping FV inactive. Mechanisms that counteract the autoinhibitory function of the PRR drive FV activation. The predominant way this occurs after the initiation of coagulation is via discrete proteolysis within the B-domain. Cleavage at these sites must destabilize or facilitate the disengagement of the PRR to enable FXa to bind to the heavy/light chain region and thus allow for prothrombinase assembly. These insights are unique and could not have been uncovered by correlating B-domain cleavage with activity development. The findings detailed here also provide the starting point for unraveling new mechanistic details of FV activation and point to novel strategies for modulation of FV/FVa function for therapeutic purposes.