Membrane Budding

被引：229

作者：

Hurley, James H. ^{[1
]}

Boura, Evzen ^{[1
]}

Carlson, Lars-Anders ^{[1
]}

Rozycki, Bartosz ^{[2
]}

机构：

[1] NIDDKD, Mol Biol Lab, NIH, Bethesda, MD 20892 USA

[2] NIDDKD, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

来源：

CELL | 2010年 / 143卷 / 06期

基金：

美国国家卫生研究院;

关键词：

HUMAN-IMMUNODEFICIENCY-VIRUS; ESCRT-III PROTEIN; VESICULAR-STOMATITIS-VIRUS; PLASMA-MEMBRANE; MATRIX PROTEIN; PHASE-SEPARATION; STRUCTURAL BASIS; LIPID RAFTS; INTRALUMENAL VESICLES; COAT PROTEINS;

D O I：

10.1016/j.cell.2010.11.030

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Membrane budding is a key step in vesicular transport, multivesicular body biogenesis, and enveloped virus release. These events range from those that are primarily protein driven, such as the formation of coated vesicles, to those that are primarily lipid driven, such as microdomain-dependent biogenesis of multivesicular bodies. Other types of budding reside in the middle of this spectrum, including caveolae biogenesis, HIV-1 budding, and ESCRT-catalyzed multivesicular body formation. Some of these latter events involve budding away from cytosol, and this unusual topology involves unique mechanisms. This Review discusses progress toward understanding the structural and energetic bases of these different membrane-budding paradigms.

引用

收藏

页码：875 / 887

页数：13

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