Recent advances in top-down proteome sample processing ahead of MS analysis

被引:38
作者
Nickerson, Jessica L. [1 ]
Baghalabadi, Venus [1 ]
Rajendran, Subin R. C. K. [1 ,2 ]
Jakubec, Philip J. [1 ]
Said, Hammam [1 ]
McMillen, Teresa S. [1 ]
Dang, Ziheng [1 ]
Doucette, Alan A. [1 ]
机构
[1] Dalhousie Univ, Dept Chem, 6274 Coburg Rd, Halifax, NS B3H 4R2, Canada
[2] Verschuren Ctr Sustainabil Energy & Environm, Sydney, NS, Canada
关键词
crude analysis; monoclonal antibodies; protein purification; capillary electrophoresis; chromatography; top-down proteomics; CAPILLARY-ZONE-ELECTROPHORESIS; SIZE-EXCLUSION CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; PHASE LIQUID-CHROMATOGRAPHY; ION MOBILITY SPECTROMETRY; INTACT MEMBRANE-PROTEINS; FIELD-FLOW FRACTIONATION; SODIUM DODECYL-SULFATE; BOTTOM-UP PROTEOMICS; LARGE-SCALE ANALYSIS;
D O I
10.1002/mas.21706
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Top-down proteomics is emerging as a preferred approach to investigate biological systems, with objectives ranging from the detailed assessment of a single protein therapeutic, to the complete characterization of every possible protein including their modifications, which define the human proteoform. Given the controlling influence of protein modifications on their biological function, understanding how gene products manifest or respond to disease is most precisely achieved by characterization at the intact protein level. Top-down mass spectrometry (MS) analysis of proteins entails unique challenges associated with processing whole proteins while maintaining their integrity throughout the processes of extraction, enrichment, purification, and fractionation. Recent advances in each of these critical front-end preparation processes, including minimalistic workflows, have greatly expanded the capacity of MS for top-down proteome analysis. Acknowledging the many contributions in MS technology and sample processing, the present review aims to highlight the diverse strategies that have forged a pathway for top-down proteomics. We comprehensively discuss the evolution of front-end workflows that today facilitate optimal characterization of proteoform-driven biology, including a brief description of the clinical applications that have motivated these impactful contributions.
引用
收藏
页码:457 / 495
页数:39
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