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Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry

Co-culture system, in which two or more distinct cell types are cultured together, is advantageous in that it can mimic the environment of the in vivo niche of the cells. In this study, we presented a strategy to analyze the secretome of a specific cell type under the co-culture condition in serum-s...

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Autores principales: Shin, Sungho, Lee, Seonjeong, Choi, Sunyoung, Park, Narae, Kwon, Yumi, Jeong, Jaehoon, Ju, Shinyeong, Chang, Yunsil, Park, Kangsik, Ha, Chulwon, Lee, Cheolju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223471/
https://www.ncbi.nlm.nih.gov/pubmed/35742968
http://dx.doi.org/10.3390/ijms23126527
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author Shin, Sungho
Lee, Seonjeong
Choi, Sunyoung
Park, Narae
Kwon, Yumi
Jeong, Jaehoon
Ju, Shinyeong
Chang, Yunsil
Park, Kangsik
Ha, Chulwon
Lee, Cheolju
author_facet Shin, Sungho
Lee, Seonjeong
Choi, Sunyoung
Park, Narae
Kwon, Yumi
Jeong, Jaehoon
Ju, Shinyeong
Chang, Yunsil
Park, Kangsik
Ha, Chulwon
Lee, Cheolju
author_sort Shin, Sungho
collection PubMed
description Co-culture system, in which two or more distinct cell types are cultured together, is advantageous in that it can mimic the environment of the in vivo niche of the cells. In this study, we presented a strategy to analyze the secretome of a specific cell type under the co-culture condition in serum-supplemented media. For the cell-specific secretome analysis, we expressed the mouse mutant methionyl-tRNA synthetase for the incorporation of the non-canonical amino acid, azidonorleucine into the newly synthesized proteins in cells of which the secretome is targeted. The azidonorleucine-tagged secretome could be enriched, based on click chemistry, and distinguished from any other contaminating proteins, either from the cell culture media or the other cells co-cultured with the cells of interest. In order to have more reliable true-positive identifications of cell-specific secretory bodies, we established criteria to exclude any identified human peptide matched to bovine proteins. As a result, we identified a maximum of 719 secreted proteins in the secretome analysis under this co-culture condition. Last, we applied this platform to profile the secretome of mesenchymal stem cells and predicted its therapeutic potential on osteoarthritis based on secretome analysis.
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spelling pubmed-92234712022-06-24 Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry Shin, Sungho Lee, Seonjeong Choi, Sunyoung Park, Narae Kwon, Yumi Jeong, Jaehoon Ju, Shinyeong Chang, Yunsil Park, Kangsik Ha, Chulwon Lee, Cheolju Int J Mol Sci Article Co-culture system, in which two or more distinct cell types are cultured together, is advantageous in that it can mimic the environment of the in vivo niche of the cells. In this study, we presented a strategy to analyze the secretome of a specific cell type under the co-culture condition in serum-supplemented media. For the cell-specific secretome analysis, we expressed the mouse mutant methionyl-tRNA synthetase for the incorporation of the non-canonical amino acid, azidonorleucine into the newly synthesized proteins in cells of which the secretome is targeted. The azidonorleucine-tagged secretome could be enriched, based on click chemistry, and distinguished from any other contaminating proteins, either from the cell culture media or the other cells co-cultured with the cells of interest. In order to have more reliable true-positive identifications of cell-specific secretory bodies, we established criteria to exclude any identified human peptide matched to bovine proteins. As a result, we identified a maximum of 719 secreted proteins in the secretome analysis under this co-culture condition. Last, we applied this platform to profile the secretome of mesenchymal stem cells and predicted its therapeutic potential on osteoarthritis based on secretome analysis. MDPI 2022-06-10 /pmc/articles/PMC9223471/ /pubmed/35742968 http://dx.doi.org/10.3390/ijms23126527 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shin, Sungho
Lee, Seonjeong
Choi, Sunyoung
Park, Narae
Kwon, Yumi
Jeong, Jaehoon
Ju, Shinyeong
Chang, Yunsil
Park, Kangsik
Ha, Chulwon
Lee, Cheolju
Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry
title Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry
title_full Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry
title_fullStr Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry
title_full_unstemmed Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry
title_short Characterization of the Secretome of a Specific Cell Expressing Mutant Methionyl-tRNA Synthetase in Co-Culture Using Click Chemistry
title_sort characterization of the secretome of a specific cell expressing mutant methionyl-trna synthetase in co-culture using click chemistry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223471/
https://www.ncbi.nlm.nih.gov/pubmed/35742968
http://dx.doi.org/10.3390/ijms23126527
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