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A convenient protein library for spectroscopic calibrations
While several Raman, CD or FTIR spectral libraries are available for well-characterized proteins of known structure, proteins themselves are usually very difficult to acquire, preventing a convenient calibration of new instruments and new recording methods. The problem is particularly critical in th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369421/ https://www.ncbi.nlm.nih.gov/pubmed/32728409 http://dx.doi.org/10.1016/j.csbj.2020.07.001 |
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author | De Meutter, Joëlle Goormaghtigh, Erik |
author_facet | De Meutter, Joëlle Goormaghtigh, Erik |
author_sort | De Meutter, Joëlle |
collection | PubMed |
description | While several Raman, CD or FTIR spectral libraries are available for well-characterized proteins of known structure, proteins themselves are usually very difficult to acquire, preventing a convenient calibration of new instruments and new recording methods. The problem is particularly critical in the field of FTIR spectroscopy where numerous new methods are becoming available on the market. The present papers reports the construction of a protein library (cSP92) including commercially available products, that are well characterized experimentally for their purity and solubility in conditions compatible with the recording of FTIR spectra and whose high-resolution structure is available. Overall, 92 proteins were selected. These proteins cover well the CATH space at the level of classes and architectures. In terms of secondary structure content, an analysis of their high-resolution structure by DSSP shows that the mean content in the different secondary structures present in cSP92 is very similar to the mean content found in the PDB. The 92-protein set is analyzed in details for the distribution of helix length, number of strands in β- sheets, length of β-strands and amino acid content, all features that may be important for the interpretation of FTIR spectra. |
format | Online Article Text |
id | pubmed-7369421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73694212020-07-28 A convenient protein library for spectroscopic calibrations De Meutter, Joëlle Goormaghtigh, Erik Comput Struct Biotechnol J Research Article While several Raman, CD or FTIR spectral libraries are available for well-characterized proteins of known structure, proteins themselves are usually very difficult to acquire, preventing a convenient calibration of new instruments and new recording methods. The problem is particularly critical in the field of FTIR spectroscopy where numerous new methods are becoming available on the market. The present papers reports the construction of a protein library (cSP92) including commercially available products, that are well characterized experimentally for their purity and solubility in conditions compatible with the recording of FTIR spectra and whose high-resolution structure is available. Overall, 92 proteins were selected. These proteins cover well the CATH space at the level of classes and architectures. In terms of secondary structure content, an analysis of their high-resolution structure by DSSP shows that the mean content in the different secondary structures present in cSP92 is very similar to the mean content found in the PDB. The 92-protein set is analyzed in details for the distribution of helix length, number of strands in β- sheets, length of β-strands and amino acid content, all features that may be important for the interpretation of FTIR spectra. Research Network of Computational and Structural Biotechnology 2020-07-10 /pmc/articles/PMC7369421/ /pubmed/32728409 http://dx.doi.org/10.1016/j.csbj.2020.07.001 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article De Meutter, Joëlle Goormaghtigh, Erik A convenient protein library for spectroscopic calibrations |
title | A convenient protein library for spectroscopic calibrations |
title_full | A convenient protein library for spectroscopic calibrations |
title_fullStr | A convenient protein library for spectroscopic calibrations |
title_full_unstemmed | A convenient protein library for spectroscopic calibrations |
title_short | A convenient protein library for spectroscopic calibrations |
title_sort | convenient protein library for spectroscopic calibrations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369421/ https://www.ncbi.nlm.nih.gov/pubmed/32728409 http://dx.doi.org/10.1016/j.csbj.2020.07.001 |
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