Yu Zhong, Koningstein Gregory, Pop Ana, Luirink Joen
Department of Molecular Microbiology, Institute of Molecular Cell Biology, VU University, de Boelelaan 1085, 1081 HV Amsterdam, The Netherlands.
J Biol Chem. 2008 Dec 12;283(50):34635-42. doi: 10.1074/jbc.M804344200. Epub 2008 Oct 6.
Escherichia coli YidC is a polytopic inner membrane protein that plays an essential and versatile role in the biogenesis of inner membrane proteins. YidC functions in Sec-dependent membrane insertion but acts also independently as a separate insertase for certain small membrane proteins. We have used a site-specific cross-linking approach to show that the conserved third transmembrane segment of YidC contacts the transmembrane domains of both nascent Sec-dependent and -independent substrates, indicating a generic recognition of insertion intermediates by YidC. Our data suggest that specific residues of the third YidC transmembrane segment alpha-helix is oriented toward the transmembrane domains of nascent inner membrane proteins that, in contrast, appear quite flexibly positioned at this stage in biogenesis.
大肠杆菌YidC是一种多跨膜内膜蛋白,在内膜蛋白的生物合成中发挥着重要且多样的作用。YidC在依赖Sec的膜插入过程中发挥作用,但对于某些小的膜蛋白,它也可作为一种独立的插入酶发挥作用。我们采用位点特异性交联方法表明,YidC保守的第三个跨膜片段与新生的依赖Sec和不依赖Sec的底物的跨膜结构域接触,这表明YidC对插入中间体具有普遍的识别作用。我们的数据表明,YidC第三个跨膜片段α螺旋的特定残基朝向新生内膜蛋白的跨膜结构域,相比之下,这些跨膜结构域在生物合成的这一阶段似乎定位相当灵活。