Indirect estimation of the area density of Atg8 on the phagophore

被引:21
作者
Xie, Zhiping [1 ,2 ]
Nair, Usha [1 ,2 ]
Geng, Jiefei [1 ,2 ]
Szefler, Maciej B. [4 ]
Rothman, Edward D. [4 ]
Klionsky, Daniel J. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Stat, Ann Arbor, MI 48109 USA
关键词
autophagy; lysosome; stress; vacuole; yeast; AUTOPHAGOSOME FORMATION; PROTEIN LIPIDATION; COMPLEX; YEAST; MICROSCOPY; CYTOPLASM; PATHWAYS; REQUIRES; FUSION; AUT7P;
D O I
10.4161/auto.5.2.7201
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Atg8 is a ubiquitin-like protein that controls the expansion of the phagophore during autophagosome formation. It is recruited to the phagophore during the expansion stage and released upon the completion of the autophagosome. One possible model explaining the function of Atg8 is that it acts as an adaptor of a coat complex. Here, we tested the coat-adaptor model by estimating the area density of Atg8 molecules on the phagophore. We developed a computational process to simulate the random sectioning of vesicles heterogeneous in size. This method can be applied to estimate the original sizes of intracellular vesicles from sizes of their random sections obtained through transmission electron microscopy. Using this method, we found that the estimated area density of Atg8 is comparable with that of proteins that form the COPII coat.
引用
收藏
页码:217 / 220
页数:4
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