Exo1: A new chemical inhibitor of the exocytic pathway

被引:126
作者
Feng, Y [1 ]
Yu, S
Lasell, TKR
Jadhav, AP
Macia, E
Chardin, P
Melancon, P
Roth, M
Mitchison, T
Kirchhausen, T
机构
[1] Harvard Univ, Sch Med, Inst Chem & Cell Biol, Dept Cell Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Ctr Blood Res, Boston, MA 02115 USA
[3] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75235 USA
[4] Univ Alberta, Dept Cell Biol, Edmonton, AB T6H 2H7, Canada
[5] CNRS, Inst Pharmacol Mol & Cellulaire, UMR 6097, F-06560 Valbonne, France
关键词
Golgi; ADP-ribosylation factor; endoplasmic reticulum (ER); imaging-based screen; Bars50;
D O I
10.1073/pnas.0631766100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A phenotypic screen was used to search for drug-like molecules that can interfere with specific steps in membrane traffic. 2-(4-Fluorobenzoylamino)-benzoic acid methyl ester (Exo1), identified in this screen, induces a rapid collapse of the Golgi to the endoplasmic reticulum, thus acutely inhibiting the traffic emanating from the endoplasmic reticulum. Like Brefeldin A (BFA), Exo1 induces the rapid release of ADP-ribosylation factor (ARIF) 1 from Golgi membranes but has less effect on the organization of the trans-Golgi network. Our data indicate that Exo1 acts by a different mechanism from BFA. Unlike BFA, Exo1 does not induce the ADP-ribosylation of CtBP/Bars50 and does not interfere with the activity of guanine nucleotide exchange factors specific for Golgi-based ARFs. Thus, Exo1 allows the fatty acid exchange activity of Bars50 to be distinguished from ARF1 activity in the control of Golgi tubulation.
引用
收藏
页码:6469 / 6474
页数:6
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