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Single-cell Proteomics: Progress and Prospects.
Kelly, Ryan T.
Afiliación
  • Kelly RT; Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah, USA. Electronic address: ryan.kelly@byu.edu.
Mol Cell Proteomics ; 19(11): 1739-1748, 2020 11.
Article en En | MEDLINE | ID: mdl-32847821
ABSTRACT
MS-based proteome profiling has become increasingly comprehensive and quantitative, yet a persistent shortcoming has been the relatively large samples required to achieve an in-depth measurement. Such bulk samples, typically comprising thousands of cells or more, provide a population average and obscure important cellular heterogeneity. Single-cell proteomics capabilities have the potential to transform biomedical research and enable understanding of biological systems with a new level of granularity. Recent advances in sample processing, separations and MS instrumentation now make it possible to quantify >1000 proteins from individual mammalian cells, a level of coverage that required an input of thousands of cells just a few years ago. This review discusses important factors and parameters that should be optimized across the workflow for single-cell and other low-input measurements. It also highlights recent developments that have advanced the field and opportunities for further development.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteómica / Análisis de la Célula Individual / RNA-Seq Límite: Humans Idioma: En Revista: Mol Cell Proteomics Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteómica / Análisis de la Célula Individual / RNA-Seq Límite: Humans Idioma: En Revista: Mol Cell Proteomics Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA Año: 2020 Tipo del documento: Article