共 56 条
Solution Structure of the ESCRT-I and -II Supercomplex: Implications for Membrane Budding and Scission
被引:73
作者:

Boura, Evzen
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h-index: 0
机构:
NIDDK, Mol Biol Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Rozycki, Bartosz
论文数: 0 引用数: 0
h-index: 0
机构:
NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Chung, Hoi Sung
论文数: 0 引用数: 0
h-index: 0
机构:
NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Herrick, Dawn Z.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Virginia, Dept Chem, Biophys Program, Charlottesville, VA 22904 USA
Univ Virginia, Ctr Membrane Biol, Charlottesville, VA 22904 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Canagarajah, Bertram
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h-index: 0
机构:
NIDDK, Mol Biol Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Cafiso, David S.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Virginia, Dept Chem, Biophys Program, Charlottesville, VA 22904 USA
Univ Virginia, Ctr Membrane Biol, Charlottesville, VA 22904 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Eaton, William A.
论文数: 0 引用数: 0
h-index: 0
机构:
NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Hummer, Gerhard
论文数: 0 引用数: 0
h-index: 0
机构:
NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA

Hurley, James H.
论文数: 0 引用数: 0
h-index: 0
机构:
NIDDK, Mol Biol Lab, NIH, Bethesda, MD 20892 USA NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
机构:
[1] NIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
[2] NIDDK, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[3] Univ Virginia, Dept Chem, Biophys Program, Charlottesville, VA 22904 USA
[4] Univ Virginia, Ctr Membrane Biol, Charlottesville, VA 22904 USA
来源:
基金:
美国国家卫生研究院;
关键词:
MULTIVESICULAR BODY BIOGENESIS;
ENDOSOME-ASSOCIATED COMPLEX;
SINGLE-MOLECULE FRET;
SORTING COMPLEX;
UBIQUITINATED PROTEINS;
TRAFFICKING COMPLEX;
GLUE DOMAIN;
MACHINERY;
TRANSPORT;
DYNAMICS;
D O I:
10.1016/j.str.2012.03.008
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:
The ESCRT-I and ESCRT-II supercomplex induces membrane buds that invaginate into the lumen of endosomes, a process central to the lysosomal degradation of ubiquitinated membrane proteins. The solution conformation. of the membrane-budding ESCRT-I-II supercomplex from yeast was refined against small-angle X-ray scattering (SAXS), single-molecule Forster resonance energy transfer (smFRET), and double electron-electron resonance (DEER) spectra. These refinements yielded an ensemble of 18 ESCRT-I-II supercomplex structures that range from compact to highly extended. The crescent shapes of the ESCRT-I-II supercomplex structures provide the basis for a detailed mechanistic model, in which ESCRT-I-II stabilizes membrane buds and coordinates cargo sorting by lining the pore of the nascent bud necks. The hybrid refinement used here is general and should be applicable to other dynamic multiprotein assmeblies.
引用
收藏
页码:874 / 886
页数:13
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