1. Academic Validation
  2. Exo1: a new chemical inhibitor of the exocytic pathway

Exo1: a new chemical inhibitor of the exocytic pathway

  • Proc Natl Acad Sci U S A. 2003 May 27;100(11):6469-74. doi: 10.1073/pnas.0631766100.
Yan Feng 1 Sidney Yu Troy K R Lasell Ashutosh P Jadhav Eric Macia Pierre Chardin Paul Melancon Michael Roth Timothy Mitchison Tomas Kirchhausen
Affiliations

Affiliation

  • 1 Institute of Chemistry and Cell Biology, Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA. yfeng@hms.harvard.edu
Abstract

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.

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  • HY-112670
    99.80%, Exocytic通路抑制剂