Sarkar Mayukh K, Husnain Seyyed I, Jakubowski Simon J, Christie Peter J
Department of Microbiology and Molecular Genetics, University of Texas Medical School at Houston, Houston, TX, USA.
Methods Mol Biol. 2013;966:187-204. doi: 10.1007/978-1-62703-245-2_12.
The bacterial type IV secretion systems (T4SSs) deliver DNA and protein substrates to bacterial and eukaryotic target cells generally by a mechanism requiring direct contact between donor and target cells. Recent advances in defining the architectures of T4SSs have been made through isolation of machine subassemblies for further biochemical and ultrastructural analysis. Here, we describe a protocol for isolation and characterization of VirB protein complexes from the paradigmatic VirB/VirD4 T4SS of Agrobacterium tumefaciens. This protocol can be adapted for isolation of T4SS subassemblies from other gram-negative bacteria as well as gram-positive bacteria. The biological importance of isolated T4SS subcomplexes can be assessed by assaying for copurification of trapped or cross-linked substrates. This can be achieved with a modified form of the chromatin immunoprecipitation (ChIP) assay termed transfer DNA immunoprecipitation (TrIP). Here, a TrIP protocol is described for recovery of formaldehyde-cross-linked DNA substrate-channel subunit complexes from cells employing T4SSs for conjugative DNA transfer.
细菌IV型分泌系统(T4SSs)通常通过一种需要供体细胞与靶细胞直接接触的机制,将DNA和蛋白质底物递送至细菌和真核靶细胞。通过分离机器亚组件以进行进一步的生化和超微结构分析,在确定T4SSs的结构方面取得了最新进展。在这里,我们描述了一种从根癌土壤杆菌典型的VirB/VirD4 T4SS中分离和鉴定VirB蛋白复合物的方案。该方案可适用于从其他革兰氏阴性菌以及革兰氏阳性菌中分离T4SS亚组件。分离的T4SS亚复合物的生物学重要性可通过检测捕获或交联底物的共纯化来评估。这可以通过一种称为转移DNA免疫沉淀(TrIP)的染色质免疫沉淀(ChIP)分析的改良形式来实现。在这里,描述了一种TrIP方案,用于从利用T4SSs进行接合DNA转移的细胞中回收甲醛交联的DNA底物-通道亚基复合物。