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Misincorporation Proteomics Technologies: A Review

Proteinopathies are diseases caused by factors that affect proteoform conformation. As such, a prevalent hypothesis is that the misincorporation of noncanonical amino acids into a proteoform results in detrimental structures. However, this hypothesis is missing proteomic evidence, specifically the d...

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Autores principales: Steele, Joel R., Italiano, Carly J., Phillips, Connor R., Violi, Jake P., Pu, Lisa, Rodgers, Kenneth J., Padula, Matthew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924376/
https://www.ncbi.nlm.nih.gov/pubmed/33494504
http://dx.doi.org/10.3390/proteomes9010002
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author Steele, Joel R.
Italiano, Carly J.
Phillips, Connor R.
Violi, Jake P.
Pu, Lisa
Rodgers, Kenneth J.
Padula, Matthew P.
author_facet Steele, Joel R.
Italiano, Carly J.
Phillips, Connor R.
Violi, Jake P.
Pu, Lisa
Rodgers, Kenneth J.
Padula, Matthew P.
author_sort Steele, Joel R.
collection PubMed
description Proteinopathies are diseases caused by factors that affect proteoform conformation. As such, a prevalent hypothesis is that the misincorporation of noncanonical amino acids into a proteoform results in detrimental structures. However, this hypothesis is missing proteomic evidence, specifically the detection of a noncanonical amino acid in a peptide sequence. This review aims to outline the current state of technology that can be used to investigate mistranslations and misincorporations whilst framing the pursuit as Misincorporation Proteomics (MiP). The current availability of technologies explored herein is mass spectrometry, sample enrichment/preparation, data analysis techniques, and the hyphenation of approaches. While many of these technologies show potential, our review reveals a need for further development and refinement of approaches is still required.
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spelling pubmed-79243762021-03-03 Misincorporation Proteomics Technologies: A Review Steele, Joel R. Italiano, Carly J. Phillips, Connor R. Violi, Jake P. Pu, Lisa Rodgers, Kenneth J. Padula, Matthew P. Proteomes Review Proteinopathies are diseases caused by factors that affect proteoform conformation. As such, a prevalent hypothesis is that the misincorporation of noncanonical amino acids into a proteoform results in detrimental structures. However, this hypothesis is missing proteomic evidence, specifically the detection of a noncanonical amino acid in a peptide sequence. This review aims to outline the current state of technology that can be used to investigate mistranslations and misincorporations whilst framing the pursuit as Misincorporation Proteomics (MiP). The current availability of technologies explored herein is mass spectrometry, sample enrichment/preparation, data analysis techniques, and the hyphenation of approaches. While many of these technologies show potential, our review reveals a need for further development and refinement of approaches is still required. MDPI 2021-01-21 /pmc/articles/PMC7924376/ /pubmed/33494504 http://dx.doi.org/10.3390/proteomes9010002 Text en © 2021 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 (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Review
Steele, Joel R.
Italiano, Carly J.
Phillips, Connor R.
Violi, Jake P.
Pu, Lisa
Rodgers, Kenneth J.
Padula, Matthew P.
Misincorporation Proteomics Technologies: A Review
title Misincorporation Proteomics Technologies: A Review
title_full Misincorporation Proteomics Technologies: A Review
title_fullStr Misincorporation Proteomics Technologies: A Review
title_full_unstemmed Misincorporation Proteomics Technologies: A Review
title_short Misincorporation Proteomics Technologies: A Review
title_sort misincorporation proteomics technologies: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924376/
https://www.ncbi.nlm.nih.gov/pubmed/33494504
http://dx.doi.org/10.3390/proteomes9010002
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