Literature DB >> 23329504

Pulse-chase analysis for studies of MHC class II biosynthesis, maturation, and peptide loading.

Tieying Hou1, Cornelia H Rinderknecht2, Andreas V Hadjinicolaou2, Robert Busch3, Elizabeth Mellins4.   

Abstract

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.

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Year:  2013        PMID: 23329504      PMCID: PMC4159250          DOI: 10.1007/978-1-62703-218-6_31

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  78 in total

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Journal:  Immunity       Date:  1996-01       Impact factor: 31.745

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Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-15       Impact factor: 11.205

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  6 in total

1.  Epitope Selection for HLA-DQ2 Presentation: Implications for Celiac Disease and Viral Defense.

Authors:  Shu-Chen Hung; Tieying Hou; Wei Jiang; Nan Wang; Shuo-Wang Qiao; I-Ting Chow; Xiaodan Liu; Sjoerd H van der Burg; David M Koelle; William W Kwok; Ludvig M Sollid; Elizabeth D Mellins
Journal:  J Immunol       Date:  2019-03-29       Impact factor: 5.422

2.  Monitoring of the Cytoskeleton-Dependent Intracellular Trafficking of Fluorescent Iron Oxide Nanoparticles by Nanoparticle Pulse-Chase Experiments in C6 Glioma Cells.

Authors:  Wiebke Willmann; Ralf Dringen
Journal:  Neurochem Res       Date:  2018-09-08       Impact factor: 3.996

3.  Accelerated turnover of MHC class II molecules in nonobese diabetic mice is developmentally and environmentally regulated in vivo and dispensable for autoimmunity.

Authors:  Alessandra De Riva; Mark C Varley; Leslie J Bluck; Anne Cooke; Michael J Deery; Robert Busch
Journal:  J Immunol       Date:  2013-05-15       Impact factor: 5.422

Review 4.  MHC Class II Protein Turnover In vivo and Its Relevance for Autoimmunity in Non-Obese Diabetic Mice.

Authors:  Alessandra De Riva; Robert Busch
Journal:  Front Immunol       Date:  2013-11-25       Impact factor: 7.561

5.  Allele-Independent Turnover of Human Leukocyte Antigen (HLA) Class Ia Molecules.

Authors:  Claudia Prevosto; M Farooq Usmani; Sarah McDonald; Aleksandra M Gumienny; Tim Key; Reyna S Goodman; J S Hill Gaston; Michael J Deery; Robert Busch
Journal:  PLoS One       Date:  2016-08-16       Impact factor: 3.240

6.  Cycloheximide Treatment Causes a ZVAD-Sensitive Protease-Dependent Cleavage of Human Tau in Drosophila Cells.

Authors:  Junhua Geng; Lu Xia; Wanjie Li; Changqi Zhao; Fei Dou
Journal:  J Alzheimers Dis       Date:  2016       Impact factor: 4.472

  6 in total

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