Self‐association of EPEC intimin mediated by the β‐barrel‐containing anchor domain: a role in clustering of the Tir receptor
Self‐association of EPEC intimin mediated by the β‐barrel‐containing anchor domain: a role in clustering of the Tir receptor
复制标题
含有 β-桶的锚结构域介导的 EPEC intimin 自缔合:在 Tir 受体聚集中的作用
作者:
T. Touzé;Richard D Hayward;J. Eswaran;J. Leong;V. Koronakis
Outer membrane intimin directs attachment of enteropathogenic Escherichia coli (EPEC) via its Tir receptor in mammalian target cell membranes. Phosphorylation of Tir triggers local actin polymerization and the formation of ‘pedestal‐like’ pseudopods. We demonstrate that the intimin protein contains three domains, a flexible N‐terminus (residues 40–188), a central membrane‐integrated β‐barrel (189–549), and a tightly folded Tir‐binding domain (550–939). Intimin was shown by electron microscopy to form ring‐like structures with a ∼7 nm external diameter and an electron dense core, and to form channels of 50picoSiemens conductance in planar lipid bilayers. Gel filtration, multiangle light scattering and cross‐linking showed that this central β‐barrel membrane‐anchoring domain directs intimin dimerization. Isothermal titration calorimetry revealed a high affinity, single‐binding site interaction of 2 : 1 stoichiometry between dimeric intimin and Tir, and modelling suggests that this interaction determines a reticular array‐like superstructure underlying receptor clustering. In support of this model, actin rearrangement induced in Tir‐primed cultured cells by intimin‐containing proteoliposomes was dependent on the concentration of both intimin and Tir, and co‐localized with clustered phosphorylated Tir.
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影响因子:
2.9
作者:
SREERAMA, N;WOODY, RW
通讯作者:
WOODY, RW
DOI:
10.1073/pnas.87.20.7839
发表时间:
1990-10-01
影响因子:
11.1
作者:
JERSE, AE;YU, J;KAPER, JB
通讯作者:
KAPER, JB
影响因子:
2.9
作者:
Sreerama, N;Woody, RW
通讯作者:
Woody, RW
DOI:
--
发表时间:
1991
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Sen,K;Nikaido,H
通讯作者:
Nikaido,H