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氨基末端带正电荷残基在确定膜蛋白拓扑结构中的作用。

Role of NH2-terminal positively charged residues in establishing membrane protein topology.

作者信息

Parks G D, Lamb R A

机构信息

Howard Hughes Medical Institute, Northwestern University, Evanston, Illinois 60208-3500.

出版信息

J Biol Chem. 1993 Sep 5;268(25):19101-9.

PMID:8103052
Abstract

The paramyxovirus HN polypeptide is a model type II membrane protein, containing an internal uncleaved signal/anchor (S/A) and is oriented in the membrane with an NH2-terminal cytoplasmic domain and COOH-terminal ectodomain (Ncyt topology). To test the role of NH2-terminal positively charged residues in directing the HN membrane topology, the 3 arginine (Arg) residues within the 17-amino-acid NH2-terminal domain were systematically converted to a glutamine or glutamate, and the topology of the mutant proteins was examined after expression in CV-1 cells. The data indicate that: (i) each of the NH2-terminal Arg residues contributes to the signal directing proper HN topology, since substitutions in any of the three positions resulted in approximately 13-23% inversion into the Nexo form; (ii) substitutions in the Arg directly flanking the signal/anchor domain resulted in slightly more inversion than those which were located more distally; and (iii) substitution with a negatively charged glutamate led to more inversion than did replacement with an uncharged glutamine. The effect of a single Arg to Glu substitution on the HN topology was enhanced when present in the context of a truncated NH2-terminal cytoplasmic tail (3 residues). A comparison of the sequences flanking the signal/anchor of well documented type III proteins showed that the majority of these proteins contain a negatively charged residue flanking the NH2-terminal side. An exception to this rule is the NB protein which contains a single positively charged Arg residue in this position. A chimeric protein containing the NB ectodomain and the HN S/A and HN ectodomain lead to a significant fraction (70%) of the chimeric protein adopting type II topology suggesting that the positive charge flanking the S/A domain is important for establishing type II topology. These data are discussed in the context of the loop model for the biogenesis of integral membrane proteins and the possible signals necessary for establishing differing orientations.

摘要

副粘病毒HN多肽是一种典型的II型膜蛋白,含有一个内部未切割的信号/锚定序列(S/A),在膜中的取向为NH2末端胞质结构域和COOH末端胞外结构域(Ncyt拓扑结构)。为了测试NH2末端带正电荷残基在指导HN膜拓扑结构中的作用,将17个氨基酸的NH2末端结构域内的3个精氨酸(Arg)残基系统地转换为谷氨酰胺或谷氨酸,并在CV-1细胞中表达后检查突变蛋白的拓扑结构。数据表明:(i)每个NH2末端Arg残基都有助于指导正确的HN拓扑结构信号,因为在三个位置中的任何一个位置进行替换都会导致约13-23%的蛋白转变为Nexo形式;(ii)紧邻信号/锚定结构域的Arg替换导致的转变略多于位于更远端的Arg替换;(iii)用带负电荷的谷氨酸替换比用不带电荷的谷氨酰胺替换导致更多的转变。当单个Arg被Glu替换存在于截短的NH2末端胞质尾巴(3个残基)的情况下,对HN拓扑结构的影响会增强。对已充分记录的III型蛋白的信号/锚定序列侧翼序列的比较表明,这些蛋白中的大多数在NH2末端侧翼含有一个带负电荷的残基。该规则的一个例外是NB蛋白,它在这个位置含有一个带正电荷的单个Arg残基。含有NB胞外结构域、HN S/A和HN胞外结构域的嵌合蛋白导致相当一部分(70%)的嵌合蛋白采用II型拓扑结构,这表明S/A结构域侧翼的正电荷对于建立II型拓扑结构很重要。在整合膜蛋白生物发生的环模型以及建立不同取向所需的可能信号的背景下讨论了这些数据。

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