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维生素K依赖性羧化作用。一种基于凝血酶原前肽γ-羧化识别位点序列的合成肽在体外是羧化酶的活性底物。

Vitamin K-dependent carboxylation. A synthetic peptide based upon the gamma-carboxylation recognition site sequence of the prothrombin propeptide is an active substrate for the carboxylase in vitro.

作者信息

Ulrich M M, Furie B, Jacobs M R, Vermeer C, Furie B C

机构信息

Center for Hemostasis and Thrombosis Research, New England Medical Center, Boston, Massachusetts 02111.

出版信息

J Biol Chem. 1988 Jul 15;263(20):9697-702.

PMID:3133366
Abstract

The vitamin K-dependent blood-clotting proteins contain a gamma-carboxylation recognition site in the propeptide, between the signal peptide and the mature protein, that directs gamma-carboxylation of specific glutamic acid residues. To develop a better substrate for the in vitro assay of the vitamin K-dependent gamma-carboxylase and to understand the substrate recognition requirements of the carboxylase, we prepared synthetic peptides based upon the structure of human proprothrombin. These peptides were employed as substrates for in vitro carboxylation using a partially purified form of the bovine liver carboxylase. A 28-residue peptide (HVFLAPQQARSLLQRVRRANTFLEEVRK), based on residues -18 to +10 in proprothrombin, includes the complete propeptide and the first 10 residues of acarboxyprothrombin. Carboxylation of this peptide is characterized by a Km of 3.6 microM. In contrast, FLEEL is carboxylated with a Km of about 2200 microM. A 10-residue peptide (ANTFLEEVRK), based on residues +1 to +10 in prothrombin, and a 20-residue peptide (ARSLLQRVRRANTFLEEVRK), based on residues -10 to +10 in proprothrombin, are also poor substrates for the carboxylase. Replacement of phenylalanine with alanine at residue 3 (equivalent to position -16 in proprothrombin) in the 28-residue peptide significantly alters the Km to 200 microM. A synthetic propeptide (HVFLAPQQARSLLQRVRRY), homologous to residues -18 to -1 in proprothrombin, inhibited carboxylation of the 28-residue peptide substrate with a Ki of 3.5 microM, but modestly stimulated the carboxylation of the 5- and 10-residue peptide substrates. These results indicate that an intact carboxylation recognition site is required for efficient in vitro carboxylation and that this site includes critical residues in region -18 to -11 of proprothrombin. The carboxylation recognition site in the propeptide binds directly to the carboxylase or to a closely associated protein.

摘要

维生素K依赖的凝血蛋白在信号肽和成熟蛋白之间的前肽中含有一个γ-羧化识别位点,该位点指导特定谷氨酸残基的γ-羧化。为了开发一种更好的用于维生素K依赖的γ-羧化酶体外测定的底物,并了解羧化酶的底物识别要求,我们基于人凝血酶原的结构制备了合成肽。这些肽被用作底物,使用部分纯化的牛肝羧化酶进行体外羧化。一种基于凝血酶原中-18至+10位残基的28个残基的肽(HVFLAPQQARSLLQRVRRANTFLEEVRK),包括完整的前肽和脱羧凝血酶原的前10个残基。该肽的羧化特征为Km为3.6μM。相比之下,FLEEL羧化的Km约为2200μM。一种基于凝血酶原中+1至+10位残基的10个残基的肽(ANTFLEEVRK)和一种基于凝血酶原中-10至+10位残基的20个残基的肽(ARSLLQRVRRANTFLEEVRK)也是羧化酶的不良底物。在28个残基的肽中,将第3位残基(相当于凝血酶原中-16位)的苯丙氨酸替换为丙氨酸,显著改变Km至200μM。一种与凝血酶原中-18至-1位残基同源的合成前肽(HVFLAPQQARSLLQRVRRY),以3.5μM的Ki抑制28个残基的肽底物的羧化,但适度刺激5个和10个残基的肽底物的羧化。这些结果表明,有效的体外羧化需要完整的羧化识别位点,并且该位点包括凝血酶原中-18至-11区域的关键残基。前肽中的羧化识别位点直接与羧化酶或紧密相关的蛋白质结合。

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