Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Lee, Seonjeong | - |
dc.contributor.author | Ju, Shinyeong | - |
dc.contributor.author | Kim, Seok Jin | - |
dc.contributor.author | Choi, Jin-Oh | - |
dc.contributor.author | Kim, Kihyun | - |
dc.contributor.author | Kim, Darae | - |
dc.contributor.author | Jeon, Eun-Seok | - |
dc.contributor.author | Lee, Cheolju | - |
dc.date.accessioned | 2024-01-19T13:32:35Z | - |
dc.date.available | 2024-01-19T13:32:35Z | - |
dc.date.created | 2022-01-10 | - |
dc.date.issued | 2021-10-26 | - |
dc.identifier.issn | 0003-2700 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/116250 | - |
dc.description.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. | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | CLEAVAGE SITES | - |
dc.subject | HUMAN PLASMA | - |
dc.subject | TRANSTHYRETIN | - |
dc.subject | PROTEINS | - |
dc.subject | PEPTIDES | - |
dc.subject | MALDI | - |
dc.subject | TOOL | - |
dc.subject | IDENTIFICATION | - |
dc.subject | GLYCOSYLATION | - |
dc.subject | PURIFICATION | - |
dc.title | tipNrich: A Tip-Based N-Terminal Proteome Enrichment Method | - |
dc.type | Article | - |
dc.identifier.doi | 10.1021/acs.analchem.1c01722 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | ANALYTICAL CHEMISTRY, v.93, no.42, pp.14088 - 14098 | - |
dc.citation.title | ANALYTICAL CHEMISTRY | - |
dc.citation.volume | 93 | - |
dc.citation.number | 42 | - |
dc.citation.startPage | 14088 | - |
dc.citation.endPage | 14098 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000711718700010 | - |
dc.identifier.scopusid | 2-s2.0-85117453099 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | CLEAVAGE SITES | - |
dc.subject.keywordPlus | HUMAN PLASMA | - |
dc.subject.keywordPlus | TRANSTHYRETIN | - |
dc.subject.keywordPlus | PROTEINS | - |
dc.subject.keywordPlus | PEPTIDES | - |
dc.subject.keywordPlus | MALDI | - |
dc.subject.keywordPlus | TOOL | - |
dc.subject.keywordPlus | IDENTIFICATION | - |
dc.subject.keywordPlus | GLYCOSYLATION | - |
dc.subject.keywordPlus | PURIFICATION | - |
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