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Detection of Nα-terminally formylated native proteins by a pan-N-formyl methionine-specific antibodyopen access

Authors
Kim, DasomSeok, Ok-HeeJu, ShinyeongKim, Sang-YoonKim, Jeong-MokLee, CheoljuHwang, Cheol-Sang
Issue Date
May-2023
Publisher
American Society for Biochemistry and Molecular Biology Inc.
Keywords
anti-fMet antibody; fMet/N-degron; mitochondrial methionyl-tRNA formyltransferase; N-formyl methionine; peptide deformylase; protein synthesis
Citation
Journal of Biological Chemistry, v.299, no.5, pp.1 - 11
Indexed
SCIE
SCOPUS
Journal Title
Journal of Biological Chemistry
Volume
299
Number
5
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/192037
DOI
10.1016/j.jbc.2023.104652
ISSN
0021-9258
Abstract
N-formyl methionine (fMet)-containing proteins are produced in bacteria, eukaryotic organelles mitochondria and plastids, and even in cytosol. However, Nα-terminally formylated proteins have been poorly characterized because of the lack of appropriate tools to detect fMet independently of downstream proximal sequences. Using a fMet-Gly-Ser-Gly-Cys peptide as an antigen, we generated a pan-fMet-specific rabbit polyclonal antibody called anti-fMet. The raised anti-fMet recognized universally and sequence context–independently Nt-formylated proteins in bacterial, yeast, and human cells as determined by a peptide spot array, dot blotting, and immunoblotting. We anticipate that the anti-fMet antibody will be broadly used to enable an understanding of the poorly explored functions and mechanisms of Nt-formylated proteins in various organisms.
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