Single-Cell Multiomics Analysis for Drug Discovery

被引:17
|
作者
Nassar, Sam F. [1 ,2 ]
Raddassi, Khadir [3 ]
Wu, Terence [4 ]
机构
[1] Brandeis Univ, Dept Biol, Waltham, MA 02453 USA
[2] IsoPlexis, Branford, CT 06405 USA
[3] Yale Sch Med, Dept Neurol, New Haven, CT 06511 USA
[4] Yale Univ, West Campus Analyt Core, West Haven, CT 06516 USA
关键词
multiomics; genomics; metabolomics; proteomics; transcriptomics; single-cell; mass spectrometry; IsoLight; COVID-19; DECISION-MAKING PROCESS; MASS CYTOMETRY; STRUCTURAL MODIFICATION; RECENT INNOVATIONS; FLOW-CYTOMETRY; PROTEOMICS; RESPONSES; SUPPORT; METABOLOMICS; SPECTROMETRY;
D O I
10.3390/metabo11110729
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Given the heterogeneity seen in cell populations within biological systems, analysis of single cells is necessary for studying mechanisms that cannot be identified on a bulk population level. There are significant variations in the biological and physiological function of cell populations due to the functional differences within, as well as between, single species as a result of the specific proteome, transcriptome, and metabolome that are unique to each individual cell. Single-cell analysis proves crucial in providing a comprehensive understanding of the biological and physiological properties underlying human health and disease. Omics technologies can help to examine proteins (proteomics), RNA molecules (transcriptomics), and the chemical processes involving metabolites (metabolomics) in cells, in addition to genomes. In this review, we discuss the value of multiomics in drug discovery and the importance of single-cell multiomics measurements. We will provide examples of the benefits of applying single-cell omics technologies in drug discovery and development. Moreover, we intend to show how multiomics offers the opportunity to understand the detailed events which produce or prevent disease, and ways in which the separate omics disciplines complement each other to build a broader, deeper knowledge base.
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页数:14
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