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侵袭素的鉴定:一种使肠道细菌能够穿透培养的哺乳动物细胞的蛋白质。

Identification of invasin: a protein that allows enteric bacteria to penetrate cultured mammalian cells.

作者信息

Isberg R R, Voorhis D L, Falkow S

出版信息

Cell. 1987 Aug 28;50(5):769-78. doi: 10.1016/0092-8674(87)90335-7.

Abstract

Bacterial strains harboring the Yersinia pseudotuberculosis inv locus were analyzed in order to investigate the mechanism of host cell penetration by an invasive pathogen. The inv locus was found to be necessary for Y. pseudotuberculosis to enter HEp-2 cells and sufficient to convert E. coli into a microorganism able to penetrate cultured cells. Both E. coli and Y. pseudotuberculosis strains harboring inv mutations were defective for entry into HEp-2 cells. Furthermore, molecular clones containing inv, and little additional DNA, converted E. coli into a microorganism that was indistinguishable from the parental Yersinia strain with regard to the entry of cultured cells. Data from in vitro protein synthesis indicated that a 103 kd protein was synthesized from inv, saturating the coding capacity of the locus. The nucleotide sequence shows an open reading frame corresponding to a protein of similar size. This protein, called invasin, is necessary for the microorganisms to penetrate HEp-2 cells, and is compartmentalized on the outer surface of the bacterium.

摘要

为了研究侵袭性病原体穿透宿主细胞的机制,对携带假结核耶尔森氏菌inv位点的细菌菌株进行了分析。发现inv位点对于假结核耶尔森氏菌进入HEp-2细胞是必需的,并且足以将大肠杆菌转化为能够穿透培养细胞的微生物。携带inv突变的大肠杆菌和假结核耶尔森氏菌菌株进入HEp-2细胞均存在缺陷。此外,含有inv且几乎没有额外DNA的分子克隆将大肠杆菌转化为一种在进入培养细胞方面与亲本耶尔森氏菌菌株无法区分的微生物。体外蛋白质合成数据表明,inv合成了一种103kd的蛋白质,该位点的编码能力已饱和。核苷酸序列显示了一个对应于类似大小蛋白质的开放阅读框。这种蛋白质称为侵袭素,是微生物穿透HEp-2细胞所必需的,并且定位于细菌的外表面。

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