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Identification of LMAN1- and SURF4-Dependent Secretory Cargoes.
Tang, Vi T; Abbineni, Prabhodh S; Veiga Leprevost, Felipe da; Basrur, Venkatesha; Khoriaty, Rami; Emmer, Brian T; Nesvizhskii, Alexey I; Ginsburg, David.
Afiliação
  • Tang VT; Department of Molecular and Integrative Physiology and Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Abbineni PS; Life Sciences Institute, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Veiga Leprevost FD; Department of Microbiology and Immunology, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois 60153, United States.
  • Basrur V; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Khoriaty R; Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Emmer BT; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Nesvizhskii AI; Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • Ginsburg D; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan 48109, United States.
J Proteome Res ; 22(11): 3439-3446, 2023 11 03.
Article em En | MEDLINE | ID: mdl-37844105
ABSTRACT
Most proteins secreted into the extracellular space are first recruited from the endoplasmic reticulum into coat protein complex II (COPII)-coated vesicles or tubules that facilitate their transport to the Golgi apparatus. Although several secreted proteins have been shown to be actively recruited into COPII vesicles and tubules by the cargo receptors LMAN1 and SURF4, the full cargo repertoire of these receptors is unknown. We now report mass spectrometry analysis of conditioned media and cell lysates from HuH7 cells CRISPR targeted to inactivate the LMAN1 or SURF4 gene. We found that LMAN1 has limited clients in HuH7 cells, whereas SURF4 traffics a broad range of cargoes. Analysis of putative SURF4 cargoes suggests that cargo recognition is governed by complex mechanisms rather than interaction with a universal binding motif..
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Retículo Endoplasmático / Proteínas de Membrana Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas de Transporte / Retículo Endoplasmático / Proteínas de Membrana Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article