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A Sample Preparation Procedure for Isobaric Labeling-Based Single-Cell Proteomics.
Marín-Vicente, Consuelo; Calvo, Enrique; Rodríguez, José Manuel; Villa Del Campo, Cristina; Sierra, Rocío; Végvári, Ákos; Zubarev, Roman A; Torres, Miguel; Vázquez, Jesús.
Afiliación
  • Marín-Vicente C; Cardiovascular Proteomics Group, Spanish National Centre for Cardiovascular Research (CNIC), Madrid, Spain. cmarin@cnic.es.
  • Calvo E; Genetic Control of Development and Organ Regeneration Group, Spanish National Centre for Cardiovascular Research (CNIC), Madrid, Spain. cmarin@cnic.es.
  • Rodríguez JM; Proteomics Unit, Spanish National Centre for Cardiovascular Research (CNIC), Madrid, Spain.
  • Villa Del Campo C; CIBER de Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain.
  • Sierra R; Proteomics Unit, Spanish National Centre for Cardiovascular Research (CNIC), Madrid, Spain.
  • Végvári Á; Genetic Control of Development and Organ Regeneration Group, Spanish National Centre for Cardiovascular Research (CNIC), Madrid, Spain.
  • Zubarev RA; Genetic Control of Development and Organ Regeneration Group, Spanish National Centre for Cardiovascular Research (CNIC), Madrid, Spain.
  • Torres M; Division of Chemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
  • Vázquez J; Division of Chemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Methods Mol Biol ; 2817: 33-43, 2024.
Article en En | MEDLINE | ID: mdl-38907145
ABSTRACT
Mass spectrometry-based proteomics has traditionally been limited by the amount of input material for analysis. Single-cell proteomics has emerged as a challenging discipline due to the ultra-high sensitivity required. Isobaric labeling-based multiplex strategies with a carrier proteome offer an approach to overcome the sensitivity limitations. Following this as the basic strategy, we show here the general workflow for preparing cells for single-cell mass spectrometry-based proteomics. This protocol can also be applied to manually isolated cells when large cells, such as cardiomyocytes, are difficult to isolate properly with conventional fluorescence-activated cell sorting (FACS) sorter methods.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteómica / Análisis de la Célula Individual Límite: Animals / Humans Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: España Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteómica / Análisis de la Célula Individual Límite: Animals / Humans Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: España Pais de publicación: Estados Unidos