Wright P S, Saudek V, Owen T J, Harbeson S L, Bitonti A J
Marion Merrell Dow Research Institute, Cincinnati, OH 45215-6300.
Biochem J. 1993 Jul 1;293 ( Pt 1)(Pt 1):263-7. doi: 10.1042/bj2930263.
Integrin binding to proteins often involves recognition of domains containing the arginine-glycine-aspartate (RGD) motif. Different binding affinities and specificities of the integrin-ligand protein interactions involve additional protein domains. The n.m.r. structure of the snake-venom protein echistatin suggested that the C-terminal portion of the molecule might be important, in addition to the RGD domain, in binding to the integrin glycoprotein IIbIIIa (GPIIbIIIa) [Saudek, Atkinson and Pelton (1991) Biochem. 30, 7369-7372]. The synthetic C-terminal peptide, echistatin-(40-49), PRNPHKGPAT, (1) inhibited binding of GPIIbIIIa to immobilized echistatin (IC50 3-6 mM), but did not inhibit binding of GPIIbIIIa to immobilized fibrinogen (up to 5 mM peptide), (2) activated GPIIbIIIa binding to fibronectin and vitronectin, usual ligands for the activated integrin, (3) activated binding of GPIIbIIIa to collagen type I and type IV, proteins not usually regarded as ligands for the integrin, and (4) stimulated 125I-fibrinogen binding by human platelets. These findings argue for an interaction of this non-RGD domain in echistatin with GPIIbIIIa, leading to activation of the integrin and extension of the ligand specificity to include immobilized collagen.
整合素与蛋白质的结合通常涉及对含有精氨酸 - 甘氨酸 - 天冬氨酸(RGD)基序的结构域的识别。整合素 - 配体蛋白相互作用的不同结合亲和力和特异性涉及其他蛋白质结构域。蛇毒蛋白echistatin的核磁共振结构表明,除了RGD结构域外,该分子的C末端部分可能在与整合素糖蛋白IIbIIIa(GPIIbIIIa)的结合中起重要作用[Saudek,Atkinson和Pelton(1991年),生物化学杂志30,7369 - 7372]。合成的C末端肽echistatin-(40 - 49),PRNPHKGPAT,(1)抑制GPIIbIIIa与固定化echistatin的结合(IC50为3 - 6 mM),但不抑制GPIIbIIIa与固定化纤维蛋白原的结合(肽浓度高达5 mM时),(2)激活GPIIbIIIa与纤连蛋白和玻连蛋白的结合,这两种是活化整合素的常见配体,(3)激活GPIIbIIIa与I型和IV型胶原蛋白的结合,这两种蛋白通常不被视为整合素的配体,以及(4)刺激人血小板对125I - 纤维蛋白原的结合。这些发现表明echistatin中的这个非RGD结构域与GPIIbIIIa相互作用,导致整合素活化并将配体特异性扩展到包括固定化胶原蛋白。