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Rho蛋白的第63位谷氨酰胺被大肠杆菌细胞毒素坏死因子-1脱酰胺化。

Gln 63 of Rho is deamidated by Escherichia coli cytotoxic necrotizing factor-1.

作者信息

Schmidt G, Sehr P, Wilm M, Selzer J, Mann M, Aktories K

机构信息

Institut für Pharmakologie und Toxikologie der Albert-Ludwigs-Universität Freiburg, Germany.

出版信息

Nature. 1997 Jun 12;387(6634):725-9. doi: 10.1038/42735.

Abstract

The actin cytoskeleton is regulated by GTP-hydrolysing proteins, the Rho GTPases, which act as molecular switches in diverse signal-transduction processes. Various bacterial toxins can inactivate Rho GTPases by ADP-ribosylation or glucosylation. Previous research has identified Rho proteins as putative targets for Escherichia coli cytotoxic necrotizing factors 1 and 2 (CNF1 and 2). These toxins induce actin assembly and multinucleation in culture cells. Here we show that treatment of RhoA with CNF1 inhibits the intrinsic GTPase activity of RhoA and completely blocks GTPase activity stimulated by the Rho-GTPase-activating protein (rhoGAP). Analysis by mass spectrometry and amino-acid sequencing of proteolytic peptides derived from CNF1-treated RhoA indicate that CNF1 induces deamidation of a glutamine residue at position 63 (Gln 63) to give constitutively active Rho protein.

摘要

肌动蛋白细胞骨架受GTP水解蛋白(Rho GTP酶)调控,Rho GTP酶在多种信号转导过程中起分子开关的作用。各种细菌毒素可通过ADP核糖基化或糖基化使Rho GTP酶失活。先前的研究已将Rho蛋白确定为大肠杆菌细胞毒性坏死因子1和2(CNF1和CNF2)的假定靶标。这些毒素可诱导培养细胞中的肌动蛋白组装和多核化。在此我们表明,用CNF1处理RhoA会抑制RhoA的内在GTP酶活性,并完全阻断由Rho GTP酶激活蛋白(rhoGAP)刺激的GTP酶活性。对来自CNF1处理的RhoA的蛋白水解肽进行质谱分析和氨基酸测序表明,CNF1诱导63位谷氨酰胺残基(Gln 63)脱酰胺,从而产生组成型活性Rho蛋白。

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