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Identifying an Abnormal Phosphorylated Adaptor by Viral Kinase Using Mass Spectrometry.
Su, Chenhe; Su, Chenhao; Zheng, Chunfu.
Afiliación
  • Su C; State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, NMPA Key Laboratory for Research and Evaluation of Innovative Drug, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan, China.
  • Su C; Department of Nephrology and Rheumatology, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
  • Zheng C; Department of Microbiology, Immunology and Infectious Diseases, University of Calgary, Calgary, AB, Canada.
Methods Mol Biol ; 2854: 29-34, 2025.
Article en En | MEDLINE | ID: mdl-39192115
ABSTRACT
Mass spectrometers are widely used to identify protein phosphorylation sites. The process usually involves selective isolation of phosphoproteins and subsequent fragmentation to identify both the peptide sequence and phosphorylation site. Immunoprecipitation could capture and purify the protein of interest, greatly reducing sample complexity before submitting it for mass spectrometry analysis. This chapter describes a method to identify an abnormal phosphorylated site of the adaptor protein by a viral kinase through immunoprecipitation followed by LC-MS/MS.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Inmunoprecipitación / Espectrometría de Masas en Tándem Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2025 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosfoproteínas / Inmunoprecipitación / Espectrometría de Masas en Tándem Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2025 Tipo del documento: Article