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In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1
N-Terminal methyltransferase 1 (NTMT1) catalyzes the N-terminal methylation of proteins with a specific N-terminal motif after methionine removal. Aberrant N-terminal methylation has been implicated in several cancers and developmental diseases. Together with motif sequence and signal peptide analys...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889141/ https://www.ncbi.nlm.nih.gov/pubmed/31857877 http://dx.doi.org/10.1039/c9sc02550b |
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author | Jia, Kaimin Huang, Gaochao Wu, Wei Shrestha, Ruben Wu, Bingbing Xiong, Yulan Li, Ping |
author_facet | Jia, Kaimin Huang, Gaochao Wu, Wei Shrestha, Ruben Wu, Bingbing Xiong, Yulan Li, Ping |
author_sort | Jia, Kaimin |
collection | PubMed |
description | N-Terminal methyltransferase 1 (NTMT1) catalyzes the N-terminal methylation of proteins with a specific N-terminal motif after methionine removal. Aberrant N-terminal methylation has been implicated in several cancers and developmental diseases. Together with motif sequence and signal peptide analyses, activity-based substrate profiling of NTMT1 utilizing (E)-hex-2-en-5-ynyl-S-adenosyl-l-methionine (Hey-SAM) revealed 72 potential targets, which include several previously confirmed ones and many unknowns. Target validation using normal and NTMT1 knock-out (KO) HEK293FT cells generated by CRISPR-Cas9 demonstrated that Obg-like ATPase 1 (OLA1), a protein involved in many critical cellular functions, is methylated in vivo by NTMT1. Additionally, Hey-SAM synthesis achieved ≥98% yield for SAH conversion. |
format | Online Article Text |
id | pubmed-6889141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-68891412019-12-19 In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1 Jia, Kaimin Huang, Gaochao Wu, Wei Shrestha, Ruben Wu, Bingbing Xiong, Yulan Li, Ping Chem Sci Chemistry N-Terminal methyltransferase 1 (NTMT1) catalyzes the N-terminal methylation of proteins with a specific N-terminal motif after methionine removal. Aberrant N-terminal methylation has been implicated in several cancers and developmental diseases. Together with motif sequence and signal peptide analyses, activity-based substrate profiling of NTMT1 utilizing (E)-hex-2-en-5-ynyl-S-adenosyl-l-methionine (Hey-SAM) revealed 72 potential targets, which include several previously confirmed ones and many unknowns. Target validation using normal and NTMT1 knock-out (KO) HEK293FT cells generated by CRISPR-Cas9 demonstrated that Obg-like ATPase 1 (OLA1), a protein involved in many critical cellular functions, is methylated in vivo by NTMT1. Additionally, Hey-SAM synthesis achieved ≥98% yield for SAH conversion. Royal Society of Chemistry 2019-08-09 /pmc/articles/PMC6889141/ /pubmed/31857877 http://dx.doi.org/10.1039/c9sc02550b Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Jia, Kaimin Huang, Gaochao Wu, Wei Shrestha, Ruben Wu, Bingbing Xiong, Yulan Li, Ping In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1 |
title |
In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1
|
title_full |
In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1
|
title_fullStr |
In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1
|
title_full_unstemmed |
In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1
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title_short |
In vivo methylation of OLA1 revealed by activity-based target profiling of NTMT1
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title_sort | in vivo methylation of ola1 revealed by activity-based target profiling of ntmt1 |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889141/ https://www.ncbi.nlm.nih.gov/pubmed/31857877 http://dx.doi.org/10.1039/c9sc02550b |
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