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...

Full description

Saved in:
Bibliographic Details
Published inTranslational oncology Vol. 27; p. 101556
Main Authors Petrosius, Valdemaras, Schoof, Erwin M.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.2023
Neoplasia Press
Elsevier
Online AccessGet full text

Cover

Loading…
More Information
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. [Display omitted]
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