Han Ying, Derré Isabelle
Department of Molecular Biophysics and Biochemistry, Yale University New Haven, CT, USA.
Department of Microbiology, Immunology and Cancer Biology, University of Virginia Charlottesville, VA, USA.
Front Cell Infect Microbiol. 2017 Mar 14;7:79. doi: 10.3389/fcimb.2017.00079. eCollection 2017.
is an obligate intracellular bacterium associated with trachoma and sexually transmitted diseases. During its intracellular developmental cycle, resides in a membrane bound compartment called the inclusion. A subset of Type III secreted effectors, the inclusion membrane proteins (Inc), are inserted into the inclusion membrane. Inc proteins are strategically positioned to promote inclusion interaction with host factors and organelles, a process required for bacterial replication, but little is known about Inc proteins function or host interacting partners. Moreover, it is unclear whether each Inc protein has a distinct function or if a subset of Inc proteins interacts with one another to perform their function. Here, we used IncD as a model to investigate Inc/Inc interaction in the context of Inc protein expression in . We developed a co-infection model system to display different tagged Inc proteins on the surface of the same inclusion. We also designed chimeric Inc proteins to delineate domains important for interaction. We showed that IncD can self-interact and that the full-length protein is required for dimerization and/or oligomerization. Altogether our approach can be generalized to any Inc protein and will help to characterize the molecular mechanisms by which Inc proteins interact with themselves and/or host factors, eventually leading to a better understanding of interaction with the mammalian host.
是一种与沙眼和性传播疾病相关的专性细胞内细菌。在其细胞内发育周期中,存在于一个称为包涵体的膜结合区室中。III型分泌效应子的一个子集,即包涵体膜蛋白(Inc),被插入到包涵体膜中。Inc蛋白的定位有助于促进包涵体与宿主因子和细胞器的相互作用,这是细菌复制所必需的过程,但对Inc蛋白的功能或宿主相互作用伙伴知之甚少。此外,尚不清楚每个Inc蛋白是否具有独特的功能,或者是否有一部分Inc蛋白相互作用以发挥其功能。在这里,我们以IncD为模型,在Inc蛋白在[细菌名称]中表达的背景下研究Inc/Inc相互作用。我们开发了一种共感染模型系统,以在同一包涵体表面展示不同标记的Inc蛋白。我们还设计了嵌合Inc蛋白来描绘对相互作用重要的结构域。我们表明IncD可以自我相互作用,并且全长蛋白是二聚化和/或寡聚化所必需的。总之,我们的方法可以推广到任何Inc蛋白,并将有助于阐明Inc蛋白与自身和/或宿主因子相互作用的分子机制,最终更好地理解[细菌名称]与哺乳动物宿主的相互作用。