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Discovery of a novel inhibitor of macropinocytosis with antiviral activity

Abstract: Several viruses hijack various forms of endocytosis in order to infect host cells. Here, we report the discovery of a molecule with antiviral properties that we named virapinib, which limits viral entry by macropinocytosis. The identification of virapinib derives from a chemical screen using high-throughput microscopy, where we identified chemical entities capable of preventing infection with a pseudotype virus expressing the spike (S) protein from SARS-CoV-2. Subsequent experiments confirmed the capacity of virapinib to inhibit infection by SARS-CoV-2, as well as by additional viruses, such as mpox virus and TBEV. Mechanistic analyses revealed that the compound inhibited macropinocytosis, limiting this entry route for the viruses. Importantly, virapinib has no significant toxicity to host cells. In summary, we present the discovery of a molecule that inhibits macropinocytosis, thereby limiting the infectivity of viruses that use this entry route such as SARS-CoV2.

 Autoría: Porebski B., Christ W., Corman A., Haraldsson M., Barz M., Lidemalm L., Häggblad M., Ilmain J., Wright S.C., Murga M., Schlegel J., Jarvius M., Lapins M., Sezgin E., Bhabha G., Lauschke V.M., Carreras-Puigvert J., Lafarga M., Klingström J., Hühn D., Fernandez-Capetillo O.,

 Fuente: Molecular Therapy, 2024, 39(9), 3012-3024

 Editorial: Academic Press/Cell Press

 Año de publicación: 2024

 Nº de páginas: 13

 Tipo de publicación: Artículo de Revista

 DOI: 10.1016/j.ymthe.2024.06.038

 ISSN: 1525-0016,1525-0024

 Url de la publicación: https://doi.org/10.1016/j.ymthe.2024.06.038

Autoría

POREBSKI, BARTLOMIEJ

CHRIST, WANDA

CORMAN, ALBA

HARALDSSON, MARTIN

BARZ, MYRIAM

LIDEMALM, LOUISE

HÄGGBLAD, MARIA

ILMAIN, JULIANA

WRIGHT, SHANE C.

MURGA, MATILDE

SCHLEGEL, JAN

JARVIUS, MALIN

LAPINS, MARIS

SEZGIN, ERDINC

BHABHA, GIRA

LAUSCHKE, VOLKER M.

CARRERAS-PUIGVERT, JORDI

KLINGSTRÖM, JONAS

HÜHN, DANIELA