Rollins C, Dahlquist F W
Cell. 1981 Aug;25(2):333-40. doi: 10.1016/0092-8674(81)90051-9.
The methyl-accepting chemotaxis proteins (MCPs) of Escherichia coli are integral membrane proteins that have been shown to undergo reversible methylation in response to the addition of attractants. We have shown that a second, rapid modification of MCPI and MCPII occurs, which is repellent-stimulated. This modification, which is not methylation, was detected because it causes a decrease in mobility of the MCPs on 7.5% SDS-polyacrylamide gels with a high acrylamide to bisacrylamide ratio. We have designated this modification as the CheB-modification, as it is dependent on the CheB gene product. The CheB-modification causes a decrease in the isoelectric point of MCPII by one or two charge groups. The CheB-modification is not necessary for the methylation, nor does it preclude methylation of the MCPs. Both the CheB-modified form and the unmodified, unmethylated forms of the MCPs are stable to treatment with base, which results in the hydrolysis of the methylesters (demethylation) of the MCPs. The potential role of CheB-modification in chemotaxis is discussed.
大肠杆菌的甲基接受趋化蛋白(MCPs)是整合膜蛋白,已证明其会因添加引诱剂而发生可逆甲基化。我们已表明,MCPI和MCPII会发生第二种快速修饰,这种修饰是由驱避剂刺激引起的。这种修饰不是甲基化,之所以能检测到,是因为它会导致MCPs在丙烯酰胺与双丙烯酰胺比例高的7.5%SDS -聚丙烯酰胺凝胶上的迁移率降低。我们将这种修饰命名为CheB修饰,因为它依赖于CheB基因产物。CheB修饰会使MCPII的等电点降低一或两个电荷基团。CheB修饰对于甲基化不是必需的,也不排除MCPs的甲基化。MCPs的CheB修饰形式和未修饰、未甲基化形式在用碱处理时都是稳定的,碱处理会导致MCPs的甲酯水解(去甲基化)。本文讨论了CheB修饰在趋化作用中的潜在作用。