| Literature DB >> 31676211 |
Nicholas Callahan1, Jennifer Tullman2, Zvi Kelman3, John Marino2.
Abstract
Proteomic analysis can be a critical bottleneck in cellular characterization. The current paradigm relies primarily on mass spectrometry of peptides and affinity reagents (i.e., antibodies), both of which require a priori knowledge of the sample. An unbiased protein sequencing method, with a dynamic range that covers the full range of protein concentrations in proteomes, would revolutionize the field of proteomics, allowing a more facile characterization of novel gene products and subcellular complexes. To this end, several new platforms based on single-molecule protein-sequencing approaches have been proposed. This review summarizes four of these approaches, highlighting advantages, limitations, and challenges for each method towards advancing as a core technology for next-generation protein sequencing.Entities:
Keywords: peptide sequencing; proteomics; single-molecule analysis
Mesh:
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Year: 2019 PMID: 31676211 PMCID: PMC7373172 DOI: 10.1016/j.tibs.2019.09.005
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807