tipNrich: A Tip-Based N-Terminal Proteome Enrichment Method
- Authors
- Lee, Seonjeong; Ju, Shinyeong; Kim, Seok Jin; Choi, Jin-Oh; Kim, Kihyun; Kim, Darae; Jeon, Eun-Seok; Lee, Cheolju
- Issue Date
- 2021-10-26
- Publisher
- AMER CHEMICAL SOC
- Citation
- ANALYTICAL CHEMISTRY, v.93, no.42, pp.14088 - 14098
- Abstract
- The mass spectrometry-based analysis of protein post-translational modifications requires large amounts of sample, complicating the analysis of samples with limited amounts of proteins such as clinical biopsies. Here, we present a tip-based N-terminal analysis method, tipNrich. The entire procedure is processed in a single pipette tip to minimize sample loss, which is so highly optimized to analyze small amounts of proteins, even femtomole-scale of a single protein. With tipNrich, we investigated various single proteins purified from different organisms using a low-resolution mass spectrometer and identified several N-terminal peptides with different Nt-modifications such as ragged N-termini. Furthermore, we applied matrix-assisted laser desorption ionization time-of-flight mass spectrometry to our method for shortening the analysis time. Moreover, we showed that our method could be utilized in disease diagnosis as exemplified by the characterization of wild-type transthyretin amyloidosis patients compared to the healthy individuals based on N-terminome profiling. In summary, tipNrich will satisfy the need of identifying N-terminal peptides even with highly scarce amounts of proteins and of having faster processing time to check the quality of protein products or to characterize N-terminal proteoform-related diseases.
- Keywords
- CLEAVAGE SITES; HUMAN PLASMA; TRANSTHYRETIN; PROTEINS; PEPTIDES; MALDI; TOOL; IDENTIFICATION; GLYCOSYLATION; PURIFICATION; CLEAVAGE SITES; HUMAN PLASMA; TRANSTHYRETIN; PROTEINS; PEPTIDES; MALDI; TOOL; IDENTIFICATION; GLYCOSYLATION; PURIFICATION
- ISSN
- 0003-2700
- URI
- https://pubs.kist.re.kr/handle/201004/116250
- DOI
- 10.1021/acs.analchem.1c01722
- Appears in Collections:
- KIST Article > 2021
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