Pulse-Chase Analysis for Studies of MHC Class II Biosynthesis, Maturation, and Peptide Loading.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 1 6 2019
pubmed: 31 5 2019
medline: 23 1 2020
Statut: ppublish

Résumé

Pulse-chase analysis is a commonly used technique for studying the synthesis, processing, and transport of proteins. Cultured cells expressing proteins of interest are allowed to take up radioactively labeled amino acids for a brief interval ("pulse"), during which all newly synthesized proteins incorporate the label. The cells are then returned to nonradioactive culture medium for various times ("chase"), during which proteins may undergo conformational changes, trafficking, or degradation. Proteins of interest are isolated (usually by immunoprecipitation) and resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and the fate of radiolabeled molecules is examined by autoradiography. This chapter describes a pulse-chase protocol suitable for studies of major histocompatibility complex (MHC) class II biosynthesis and maturation. We discuss how results are affected by the recognition by certain anti-class II antibodies of distinct class II conformations associated with particular biosynthetic states. Our protocol can be adapted to follow the fate of many other endogenously synthesized proteins, including viral or transfected gene products, in cultured cells.

Identifiants

pubmed: 31147950
doi: 10.1007/978-1-4939-9450-2_23
doi:

Substances chimiques

Antibodies 0
Detergents 0
Histocompatibility Antigens Class II 0
Peptides 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

315-341

Subventions

Organisme : NIAID NIH HHS
ID : F32 AI082900
Pays : United States
Organisme : Arthritis Research UK
Pays : United Kingdom

Auteurs

Tieying Hou (T)

Program in Immunology, Department of Pediatrics, Stanford University Medical School, Stanford, CA, USA.
Department of Pathology, MD Anderson Cancer Center, Houston, TX, USA.

Cornelia Rinderknecht (C)

Program in Immunology, Department of Pediatrics, Stanford University Medical School, Stanford, CA, USA.
Department of Translational Immunology, Genentech, South San Francisco, CA, USA.

Debopam Ghosh (D)

Program in Immunology, Department of Pediatrics, Stanford University Medical School, Stanford, CA, USA.

Andreas V Hadjinicolaou (AV)

Program in Immunology, Department of Pediatrics, Stanford University Medical School, Stanford, CA, USA.
MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.

Robert Busch (R)

Department of Life Sciences, University of Roehampton, London, UK. robert.busch@roehampton.ac.uk.

Elizabeth D Mellins (ED)

Program in Immunology, Department of Pediatrics, Stanford University Medical School, Stanford, CA, USA. mellins@stanford.edu.

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Classifications MeSH