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Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods
With the accumulation of next generation sequencing data, there is increasing interest in the study of intra-species difference in molecular biology, especially in relation to disease analysis. Furthermore, the dynamics of the protein is being identified as a critical factor in its function. Althoug...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821635/ https://www.ncbi.nlm.nih.gov/pubmed/24132151 http://dx.doi.org/10.3390/ijms141020635 |
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author | Pi, Jaewoo Sael, Lee |
author_facet | Pi, Jaewoo Sael, Lee |
author_sort | Pi, Jaewoo |
collection | PubMed |
description | With the accumulation of next generation sequencing data, there is increasing interest in the study of intra-species difference in molecular biology, especially in relation to disease analysis. Furthermore, the dynamics of the protein is being identified as a critical factor in its function. Although accuracy of protein structure prediction methods is high, provided there are structural templates, most methods are still insensitive to amino-acid differences at critical points that may change the overall structure. Also, predicted structures are inherently static and do not provide information about structural change over time. It is challenging to address the sensitivity and the dynamics by computational structure predictions alone. However, with the fast development of diverse mass spectrometry coupled experiments, low-resolution but fast and sensitive structural information can be obtained. This information can then be integrated into the structure prediction process to further improve the sensitivity and address the dynamics of the protein structures. For this purpose, this article focuses on reviewing two aspects: the types of mass spectrometry coupled experiments and structural data that are obtainable through those experiments; and the structure prediction methods that can utilize these data as constraints. Also, short review of current efforts in integrating experimental data in the structural modeling is provided. |
format | Online Article Text |
id | pubmed-3821635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-38216352013-11-11 Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods Pi, Jaewoo Sael, Lee Int J Mol Sci Review With the accumulation of next generation sequencing data, there is increasing interest in the study of intra-species difference in molecular biology, especially in relation to disease analysis. Furthermore, the dynamics of the protein is being identified as a critical factor in its function. Although accuracy of protein structure prediction methods is high, provided there are structural templates, most methods are still insensitive to amino-acid differences at critical points that may change the overall structure. Also, predicted structures are inherently static and do not provide information about structural change over time. It is challenging to address the sensitivity and the dynamics by computational structure predictions alone. However, with the fast development of diverse mass spectrometry coupled experiments, low-resolution but fast and sensitive structural information can be obtained. This information can then be integrated into the structure prediction process to further improve the sensitivity and address the dynamics of the protein structures. For this purpose, this article focuses on reviewing two aspects: the types of mass spectrometry coupled experiments and structural data that are obtainable through those experiments; and the structure prediction methods that can utilize these data as constraints. Also, short review of current efforts in integrating experimental data in the structural modeling is provided. Molecular Diversity Preservation International (MDPI) 2013-10-15 /pmc/articles/PMC3821635/ /pubmed/24132151 http://dx.doi.org/10.3390/ijms141020635 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Pi, Jaewoo Sael, Lee Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods |
title | Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods |
title_full | Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods |
title_fullStr | Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods |
title_full_unstemmed | Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods |
title_short | Mass Spectrometry Coupled Experiments and Protein Structure Modeling Methods |
title_sort | mass spectrometry coupled experiments and protein structure modeling methods |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821635/ https://www.ncbi.nlm.nih.gov/pubmed/24132151 http://dx.doi.org/10.3390/ijms141020635 |
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