Purification of Recombinant ESCRT-III Proteins and Their Use in Atomic Force Microscopy and In Vitro Binding and Phosphorylation Assays.
Purification of Recombinant ESCRT-III Proteins and Their Use in Atomic Force Microscopy and In Vitro Binding and Phosphorylation Assays.
复制标题
重组 ESCRT-III 蛋白的纯化及其在原子力显微镜以及体外结合和磷酸化测定中的应用。
DOI:
10.1007/978-1-4939-9492-2_15
复制
发表时间:
2019
期刊:
影响因子:
--
通讯作者:
Capalbo L
中科院分区:
文献类型:
--
作者:
Capalbo L
The endosomal sorting complex required for transport (ESCRT)-III proteins are known to assemble into filaments that mediate membrane remodeling and fission in various biological processes, including the formation of endosomal multivesicular bodies, viral budding, cytokinesis, plasma membrane repair, nuclear pore quality control, nuclear envelope reformation, and neuron pruning. The study of the regulation and function of ESCRT-III proteins is therefore crucial to understand these events and requires a combination of in vivo and in vitro experimental techniques. Here we describe two protocols for the purification of human andDrosophilaESCRT-III proteins from bacteria and their use in in vitro phosphorylation assays and atomic force microscopy experiments on membrane lipid bilayers. These protocols can also be applied for the purification of other proteins that are insoluble when expressed in bacteria.
影响因子:
56.9
作者:
Guizetti, Julien;Schermelleh, Lothar;Gerlich, Daniel W.
通讯作者:
Gerlich, Daniel W.
DOI:
10.17863/cam.6710
发表时间:
2016
期刊:
--
影响因子:
--
作者:
Capalbo L
通讯作者:
Capalbo L
影响因子:
5.6
作者:
Bhutta MS;McInerny CJ;Gould GW
通讯作者:
Gould GW