Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK; School of Life Sciences & Department of Chemistry, University of Warwick, Gibbet Hill Campus, Coventry CV4 7AL, UK.
Structure. 2020 Apr 7;28(4):475-487.e3. doi: 10.1016/j.str.2020.01.012. Epub 2020 Feb 12.
Escherichia coli lipoprotein precursors at the inner membrane undergo three maturation stages before transport by the Lol system to the outer membrane. Here, we develop a pipeline to simulate the membrane association of bacterial lipoproteins in their four maturation states. This has enabled us to model and simulate 81 of the predicted 114 E. coli lipoproteins and reveal their interactions with the host lipid membrane. As part of this set we characterize the membrane contacts of LolB, the lipoprotein involved in periplasmic translocation. We also consider the means and bioenergetics for lipoprotein localization. Our calculations uncover a preference for LolB over LolA and therefore indicate how a lipoprotein may be favorably transferred from the inner to outer membrane. Finally, we reveal that LolC has a role in membrane destabilization, thereby promoting lipoprotein transfer to LolA.
大肠杆菌脂蛋白前体在内膜经历三个成熟阶段,然后通过 Lol 系统转运到外膜。在这里,我们开发了一个管道来模拟细菌脂蛋白在其四个成熟状态下的膜结合。这使我们能够对 114 个预测的大肠杆菌脂蛋白中的 81 个进行建模和模拟,并揭示它们与宿主脂质膜的相互作用。作为其中的一部分,我们对 LolB 进行了膜接触的特征分析,LolB 是参与周质易位的脂蛋白。我们还考虑了脂蛋白定位的方法和生物能量学。我们的计算揭示了 LolB 相对于 LolA 的偏好,因此表明了脂蛋白如何从内膜有利地转移到外膜。最后,我们揭示了 LolC 在膜去稳定化中起作用,从而促进脂蛋白向 LolA 的转移。