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Electrostatic influence on IL-1 transport through the GSDMD pore.
Xie, Wen Jun; Xia, Shiyu; Warshel, Arieh; Wu, Hao.
Afiliación
  • Xie WJ; Department of Chemistry, University of Southern California, Los Angeles, CA 90089.
  • Xia S; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.
  • Warshel A; Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, MA 02115.
  • Wu H; Department of Chemistry, University of Southern California, Los Angeles, CA 90089; warshel@usc.edu wu@crystal.harvard.edu.
Proc Natl Acad Sci U S A ; 119(6)2022 02 08.
Article en En | MEDLINE | ID: mdl-35115408
ABSTRACT
A variety of signals, including inflammasome activation, trigger the formation of large transmembrane pores by gasdermin D (GSDMD). There are primarily two functions of the GSDMD pore, to drive lytic cell death, known as pyroptosis, and to permit the release of leaderless interleukin-1 (IL-1) family cytokines, a process that does not require pyroptosis. We are interested in the mechanism by which the GSDMD pore channels IL-1 release from living cells. Recent studies revealed that electrostatic interaction, in addition to cargo size, plays a critical role in GSDMD-dependent protein release. Here, we determined computationally that to enable electrostatic filtering against pro-IL-1ß, acidic lipids in the membrane need to effectively neutralize positive charges in the membrane-facing patches of the GSDMD pore. In addition, we predicted that salt has an attenuating effect on electrostatic filtering and then validated this prediction using a liposome leakage assay. A calibrated electrostatic screening factor is necessary to account for the experimental observations, suggesting that ion distribution within the pore may be different from the bulk solution. Our findings corroborate the electrostatic influence of IL-1 transport exerted by the GSDMD pore and reveal extrinsic factors, including lipid and salt, that affect the electrostatic environment.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Interleucina-1 / Proteínas de Unión a Fosfato / Proteínas Citotóxicas Formadoras de Poros Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Interleucina-1 / Proteínas de Unión a Fosfato / Proteínas Citotóxicas Formadoras de Poros Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2022 Tipo del documento: Article