z-logo
open-access-imgOpen Access
Exo1: A new chemical inhibitor of the exocytic pathway
Author(s) -
Yan Feng,
Sidney Yu,
Troy K. R. Lasell,
Ashutosh P. Jadhav,
Eric Macia,
Pierre Teilhard de Chardin,
Paul Melançon,
Michael G. Roth,
Timothy J. Mitchison,
Tomas Kirchhausen
Publication year - 2003
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0631766100
Subject(s) - brefeldin a , endoplasmic reticulum , golgi apparatus , adp ribosylation factor , microbiology and biotechnology , guanine nucleotide exchange factor , secretory pathway , biology , chemistry , biochemistry , gtpase
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 (ARF) 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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom