Exo1: A New Chemical Inhibitor of the Exocytic Pathway

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...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2003-05, Vol.100 (11), p.6469-6474
Hauptverfasser: Feng, Yan, Yu, Sidney, Troy K. R. Lasell, Jadhav, Ashutosh P., Macia, Eric, Chardin, Pierre, Melancon, Paul, Roth, Michael, Mitchison, Timothy, Kirchhausen, Tomas
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Sprache:eng
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Zusammenfassung: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.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.0631766100