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A组链球菌M6蛋白细胞相关区域的分离与特性分析

Isolation and characterization of the cell-associated region of group A streptococcal M6 protein.

作者信息

Pancholi V, Fischetti V A

机构信息

Rockefeller University, New York, New York 10021.

出版信息

J Bacteriol. 1988 Jun;170(6):2618-24. doi: 10.1128/jb.170.6.2618-2624.1988.

Abstract

DNA sequence analysis of the complete M6 protein gene revealed 19 hydrophobic amino acids at the C terminus which could act as a membrane anchor and an adjacent proline- and glycine-rich region likely to be located in the cell wall. To define this region within the cell wall and its role in attaching the molecule to the cell, we isolated the cell-associated fragment of the M protein. Assuming that the cell-associated region of the M protein would be embedded within the wall and thus protected from trypsin digestion, cells were digested with this enzyme, and the wall-associated M protein fragment was released by phage lysin digestion of the peptidoglycan. With antibody probes prepared to synthetic peptides of C-terminal sequences, a cell wall-associated M protein fragment (molecular weight, 16,000) was identified and purified. Amino acid sequence analysis placed the N terminus of the 16,000-molecular-weight fragment at residue 298 within the M sequence. Amino acid composition of this peptide was consistent with a C-terminal sequence lacking the membrane anchor. Antibody studies of nitrous acid-extracted whole bacteria suggested that, in addition to the peptidoglycan-associated region, a 65-residue helical segment of the C-terminal domain of the M protein is embedded within the carbohydrate moiety of the cell wall. Since no detectable amino sugars were associated with the wall-associated fragment, the C-terminal region of the M6 molecule is likely to be intercalated within the cross-linked peptidoglycan and not covalently linked to it. Because the C-terminal region of the M molecule is highly homologous to the C-terminal end of protein A from staphylococci and protein G from streptococci, it is likely that the mechanism of attachment of these proteins to the cell wall is conserved.

摘要

对完整的M6蛋白基因进行DNA序列分析发现,其C末端有19个疏水氨基酸,可作为膜锚定结构,且相邻的富含脯氨酸和甘氨酸的区域可能位于细胞壁中。为了确定细胞壁内的这一区域及其在将分子附着到细胞上的作用,我们分离了M蛋白的细胞相关片段。假定M蛋白的细胞相关区域会嵌入细胞壁内,从而免受胰蛋白酶消化,用该酶消化细胞,通过噬菌体溶素对肽聚糖的消化释放出与壁相关的M蛋白片段。用针对C末端序列合成肽制备的抗体探针,鉴定并纯化了一种与细胞壁相关的M蛋白片段(分子量为16,000)。氨基酸序列分析将16,000分子量片段的N末端定位在M序列中的第298位残基处。该肽的氨基酸组成与缺少膜锚定结构的C末端序列一致。对亚硝酸提取的全菌进行的抗体研究表明,除了与肽聚糖相关的区域外,M蛋白C末端结构域的一个65个残基的螺旋片段嵌入细胞壁的碳水化合物部分内。由于与壁相关片段未检测到氨基糖,M6分子的C末端区域可能插入交联的肽聚糖内,而非与之共价连接。因为M分子的C末端区域与葡萄球菌的蛋白A和链球菌的蛋白G的C末端高度同源,这些蛋白附着到细胞壁的机制可能是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd7/211179/b40ba531580a/jbacter00184-0213-a.jpg

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