Electrostatic steering and ionic tethering in the formation of thrombin-hirudin complexes: The role of the thrombin anion-binding exosite-I

被引:46
作者
Myles, T
Le Bonniec, BF
Betz, A
Stone, SR
机构
[1] Univ Cambridge, Ctr Mrc, Dept Haematol, Cambridge CB2 2QH, England
[2] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3168, Australia
关键词
D O I
10.1021/bi0023549
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electrostatic interactions between the thrombin anion-binding exosite-I (ABE-I) and the hirudin C-terminal tail play an important role in the formation of the thrombin-hirudin inhibitor complex and serves as a model for the interactions of thrombin with its many other ligands. The role of each solvent exposed basic residue in ABE-I (Arg(35), Lys(36), Arg(67), Arg(73), Arg(75) Arg(77a), LyS(81), LyS(109), Lys(110), and Lys(149e)) in electrostatic steering and ionic tethering in the formation of thrombin-hirudin inhibitor complexes was explored by site directed mutagenesis. The contribution to the binding energy (DeltaG(b)(o)) by each residue varied from 1.9 kJ mol(-1) (Lys(110)) to 15.3 kJ mol(-1) (Arg(73)) and were in general agreement to their observed interactions with hirudin residues in the thrombin-hirudin crystal structure [Rydel, T. J., Tulinsky, A., Bode, W., and Huber, R. (1991) J. Mol. Biol. 221, 583-601]. Coupling energies (Delta DeltaG(int)(o)) were calculated for the major ion-pair interactions involved in ionic tethering using complementary hirudin mutants (h-D55N, h-E57Q, and h-E58Q). Cooperativity was seen for the h-Asp(55)/Arg(73) ion pair (Delta DeltaG(int)(o) 2.4 kJ mol(-1)); however, low coupling energies for h-Asp(55)/Lys(149e) (Delta DeltaG(int)(o) 0.6 kJ mol-L) and h-Glu(58)/ Arg(77a) (Delta DeltaG(int)(o) 0.9 kJ mol(-1)) suggest these are not major interactions, as anticipated by the crystal structure. Interestingly, high coupling energies were seen for the intermolecular ion-pair h-Glu(57)/Arg(75) ( Delta DeltaG(int)(o), 2.3 kJ mol(-1)) and for the solvent bridge h-Glu(57)/Arg(77a) (Delta DeltaG(int)(o), 2.7 kJ mol(-1)) indicating that h-Glu(57) interacts directly with both Arg(75) and Arg(77a) in the thrombin-hirudin inhibitor complex. The remaining ABE-I residues that do not form major contacts in tethering the C-terminal tail of hirudin make small but collectively important contributions to the overall positive electrostatic field generated by ABE-I important in electrostatic steering.
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页码:4972 / 4979
页数:8
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