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蛋白S的凝血酶敏感区域介导了与凝血因子Xa的磷脂依赖性相互作用。

The thrombin-sensitive region of protein S mediates phospholipid-dependent interaction with factor Xa.

作者信息

Yegneswaran Subramanian, Hackeng Tilman M, Dawson Philip E, Griffin John H

机构信息

Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

J Biol Chem. 2008 Nov 28;283(48):33046-52. doi: 10.1074/jbc.M806527200. Epub 2008 Sep 10.

Abstract

To test the hypothesis that factor Xa (fXa) interacts with protein S, fXa was labeled active-site specifically with a dansyl (D) dye via a Glu-Gly-Arg (EGR) tether to yield DEGR-fXa(i). When protein S was added to phosphatidylcholine/phosphatidylserine (PC/PS, 4:1) vesicle-bound DEGR-fXa(i), the anisotropy of the dansyl moiety was altered from 0.219 +/- 0.002 to 0.245 +/- 0.003. This change in dansyl anisotropy was not observed when DEGR-Xa(i) was titrated with protein S in the absence of PC/PS vesicles, or in the presence of 100% PC vesicles, or when PC/PS vesicle-bound DEGR-fXa(i) was titrated with thrombin-cleaved protein S. The protein S-dependent dansyl fluorescence change was specific for fXa because it was not observed for two homologous and similarly labeled DEGR-fIXa(i) and DEGR-fVIIa(i). Furthermore, protein S specifically and saturably altered the fluorescence anisotropy of PC/PS-bound active site-labeled LWB-FPR-fXa(i) (Kd = 33 nm) and was photocross-linked to PC/PS-bound LWB-FPR-fXa(i) analog, independently confirming the above results. Chemically synthesized microprotein S, comprising residues 1-116 of protein S and including the gamma-carboxyglutamic-rich domain, the thrombin-sensitive region (TSR), and the first epidermal growth factor-like domain (EGF1) of protein S, altered the anisotropy of PC/PS-bound DEGR-fXa(i) from 0.219 to 0.242, similar to the effect of the protein S titration (Kd = 303 nm), suggesting that microprotein S binds to DEGR-fXa(i). To identify individual protein S domain(s) that binds DEGR-fXa(i), the EGF1 and TSR domains were chemically synthesized and studied. The TSR altered the anisotropy of DEGR-fXa(i) by approximately 16% (Kd = 3.9 microm), but the EGF1 domain had no effect on the signal. In controls, the TSR domain did not alter the anisotropy of DEGR-fIXa(i) and DEGR-fVIIa(i), respectively. These data demonstrate that membrane-bound fXa binding to protein S involves the TSR of protein S.

摘要

为了验证因子Xa(fXa)与蛋白S相互作用的假说,通过Glu-Gly-Arg(EGR)连接子用丹磺酰(D)染料特异性标记fXa的活性位点,以产生DEGR-fXa(i)。当将蛋白S添加到磷脂酰胆碱/磷脂酰丝氨酸(PC/PS,4:1)囊泡结合的DEGR-fXa(i)中时,丹磺酰部分的各向异性从0.219±0.002变为0.245±0.003。当在没有PC/PS囊泡的情况下、在存在100% PC囊泡的情况下用蛋白S滴定DEGR-Xa(i)时,或者当用凝血酶切割的蛋白S滴定PC/PS囊泡结合的DEGR-fXa(i)时,未观察到丹磺酰各向异性的这种变化。蛋白S依赖性的丹磺酰荧光变化对fXa具有特异性,因为对于两种同源且类似标记的DEGR-fIXa(i)和DEGR-fVIIa(i)未观察到这种变化。此外,蛋白S特异性且饱和地改变了PC/PS结合的活性位点标记的LWB-FPR-fXa(i)(Kd = 33 nm)的荧光各向异性,并与PC/PS结合的LWB-FPR-fXa(i)类似物发生光交联,独立地证实了上述结果。化学合成的微蛋白S,包含蛋白S的1至116位残基,包括富含γ-羧基谷氨酸的结构域、凝血酶敏感区(TSR)和蛋白S的第一个表皮生长因子样结构域(EGF1),将PC/PS结合的DEGR-fXa(i)的各向异性从0.219改变为0.242,类似于蛋白S滴定的效果(Kd = 303 nm),表明微蛋白S与DEGR-fXa(i)结合。为了鉴定与DEGR-fXa(i)结合的单个蛋白S结构域,对EGF1和TSR结构域进行了化学合成并进行了研究。TSR使DEGR-fXa(i)的各向异性改变了约16%(Kd = 3.9微米),但EGF1结构域对信号没有影响。在对照中,TSR结构域分别未改变DEGR-fIXa(i)和DEGR-fVIIa(i)的各向异性。这些数据表明,膜结合的fXa与蛋白S的结合涉及蛋白S的TSR。

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