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Endosomal Sorting Complex Required for Transport (ESCRT) Complexes Induce Phase-separated Microdomains in Supported Lipid Bilayers

机译:运输(ESCRT)复合物所需的内体分选复合物在支持的脂质双层中诱导相分离的微区。

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摘要

The endosomal sorting complex required for transport (ESCRT) system traffics ubiquitinated cargo to lysosomes via an unusual membrane budding reaction that is directed away from the cytosol. Here, we show that human ESCRT-II self-assembles into clusters of 10–100 molecules on supported lipid bilayers. The ESCRT-II clusters are functional in that they bind to ubiquitin and the ESCRT-III subunit VPS20 at nanomolar concentrations on membranes with the same stoichiometries observed in solution and in crystals. The clusters only form when cholesterol is included in the lipid mixture at >10 mol %. The clusters induce the formation of ordered membrane domains that exclude the dye 1,1′-dioctadecyl-3,3,3′,3′-tetramethylindodicarbo-cyanine perchlorate. These results show that ESCRT complexes are capable of inducing lateral lipid phase separation under conditions where the lipids themselves do not spontaneously phase-separate. This property could facilitate ESCRT-mediated membrane budding.
机译:运输所需的内体分选复合物(ESCRT)系统会通过一种异常的膜出芽反应将泛素化的货物运输到溶酶体,该膜芽接反应直接远离细胞质。在这里,我们显示了人类ESCRT-II在支持的脂质双层上自组装成10-100个分子的簇。 ESCRT-II簇具有功能性,因为它们以纳摩尔浓度结合膜上的泛素和ESCRT-III亚基VPS20,在溶液和晶体中观察到的化学计量相同。仅当脂质混合物中胆固醇的含量> 10 mol%时才会形成团簇。簇诱导形成有序的膜结构域,该结构域排除了染料1,1'-二十八烷基-3,3,3',3'-四甲基茚二碳-花青高氯酸盐。这些结果表明,在脂质本身不自发相分离的条件下,ESCRT复合物能够诱导脂质侧向相分离。该性质可以促进ESCRT介导的膜出芽。

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