Small Molecules for Dissecting Endomembrane Trafficking: A Cross-Systems View

被引:34
作者
Mishev, Kiril [1 ,2 ,3 ]
Dejonghe, Wim [1 ,2 ]
Russinova, Eugenia [1 ,2 ]
机构
[1] Univ Ghent VIB, Dept Plant Syst Biol, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Plant Biotechnol & Bioinformat, B-9052 Ghent, Belgium
[3] Bulgarian Acad Sci, Inst Plant Physiol & Genet, Sofia 1113, Bulgaria
来源
CHEMISTRY & BIOLOGY | 2013年 / 20卷 / 04期
关键词
GOLGI NETWORK/EARLY ENDOSOME; CHEMICAL GENETICS; SECRETORY PATHWAY; PLANT-CELLS; IDENTIFICATION; INHIBITOR; PROTEIN; AUTOPHAGY; RECEPTOR; TARGET;
D O I
10.1016/j.chembiol.2013.03.009
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
Endomembrane trafficking has a key role for ensuring homeostasis, growth and development, hormonal signaling, and adaptation of eukaryotes to the constantly changing environmental conditions. The complex organization of the endomembrane system implies the need for searching novel tools to specifically probe the regulatory components and dissect the tightly interconnected vesicle transport pathways. Here, we review the large-scale chemical genetic screens, which led to the identification of small molecules with an impact on various parts of the vesicle trafficking network. We discuss the similarities and differences in the organization of the endomembrane systems in yeasts, mammals, and plants based on studies of small molecules and their effects on trafficking hubs, routes, and conserved protein targets.
引用
收藏
页码:475 / 486
页数:12
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