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Study of polytopic membrane protein topological organization as a function of membrane lipid composition

机译:多孔膜蛋白拓扑组织作为膜脂组合物的函数研究

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摘要

A protocol is described using lipid mutants and thiol-specific chemical reagents to study lipid-dependent and host-specific membrane protein topogenesis by the substituted-cysteine accessibility method as applied to transmembrane domains (SCAMTM). SCAMTM is adapted to follow changes in membrane protein topology as a function of changes in membrane lipid composition. The strategy described can be adapted to any membrane system.

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