Recent advances in the field of single-cell proteomics
•Optimization of sample preparation and implementation of ion mobility approaches played a pivotal role in the rise of single-cell proteomics.•The field is rapidly advancing with improvements in both quantified proteome depth and sample throughput.•With the emergence of scp-MS the complete character...
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Published in | Translational oncology Vol. 27; p. 101556 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.01.2023
Neoplasia Press Elsevier |
Online Access | Get full text |
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Summary: | •Optimization of sample preparation and implementation of ion mobility approaches played a pivotal role in the rise of single-cell proteomics.•The field is rapidly advancing with improvements in both quantified proteome depth and sample throughput.•With the emergence of scp-MS the complete characterization of the central dogma of biology (i.e. DNA to RNA to Protein) at single cell level is on the horizon.•The field of scp-MS has reached a point of real biological application.
The field of single-cell omics is rapidly progressing. Although DNA and RNA sequencing-based methods have dominated the field to date, global proteome profiling has also entered the main stage. Single-cell proteomics was facilitated by advancements in different aspects of mass spectrometry (MS)-based proteomics, such as instrument design, sample preparation, chromatography and ion mobility. Single-cell proteomics by mass spectrometry (scp-MS) has moved beyond being a mere technical development, and is now able to deliver actual biological application and has been successfully applied to characterize different cell states. Here, we review some key developments of scp-MS, provide a background to the field, discuss the various available methods and foresee possible future directions.
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1936-5233 1936-5233 |
DOI: | 10.1016/j.tranon.2022.101556 |