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Methyl group assignment using pseudocontact shifts with PARAssign
A new version of the program PARAssign has been evaluated for assignment of NMR resonances of the 76 methyl groups in leucines, isoleucines and valines in a 25 kDa protein, using only the structure of the protein and pseudocontact shifts (PCS) generated with a lanthanoid tag at up to three attachmen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736784/ https://www.ncbi.nlm.nih.gov/pubmed/29181729 http://dx.doi.org/10.1007/s10858-017-0136-3 |
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author | Lescanne, Mathilde Skinner, Simon P. Blok, Anneloes Timmer, Monika Cerofolini, Linda Fragai, Marco Luchinat, Claudio Ubbink, Marcellus |
author_facet | Lescanne, Mathilde Skinner, Simon P. Blok, Anneloes Timmer, Monika Cerofolini, Linda Fragai, Marco Luchinat, Claudio Ubbink, Marcellus |
author_sort | Lescanne, Mathilde |
collection | PubMed |
description | A new version of the program PARAssign has been evaluated for assignment of NMR resonances of the 76 methyl groups in leucines, isoleucines and valines in a 25 kDa protein, using only the structure of the protein and pseudocontact shifts (PCS) generated with a lanthanoid tag at up to three attachment sites. The number of reliable assignments depends strongly on two factors. The principle axes of the magnetic susceptibility tensors of the paramagnetic centers should not be parallel so as to avoid correlated PCS. Second, the fraction of resonances in the spectrum of a paramagnetic sample that can be paired with the diamagnetic counterparts is critical for the assignment. With the data from two tag positions a reliable assignment could be obtained for 60% of the methyl groups and for many of the remaining resonances the number of possible assignments is limited to two or three. With a single tag, reliable assignments can be obtained for methyl groups with large PCS near the tag. It is concluded that assignment of methyl group resonances by paramagnetic tagging can be particularly useful in combination with some additional data, such as from mutagenesis or NOE-based experiments. Approaches to yield the best assignment results with PCS generating tags are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10858-017-0136-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5736784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-57367842017-12-29 Methyl group assignment using pseudocontact shifts with PARAssign Lescanne, Mathilde Skinner, Simon P. Blok, Anneloes Timmer, Monika Cerofolini, Linda Fragai, Marco Luchinat, Claudio Ubbink, Marcellus J Biomol NMR Article A new version of the program PARAssign has been evaluated for assignment of NMR resonances of the 76 methyl groups in leucines, isoleucines and valines in a 25 kDa protein, using only the structure of the protein and pseudocontact shifts (PCS) generated with a lanthanoid tag at up to three attachment sites. The number of reliable assignments depends strongly on two factors. The principle axes of the magnetic susceptibility tensors of the paramagnetic centers should not be parallel so as to avoid correlated PCS. Second, the fraction of resonances in the spectrum of a paramagnetic sample that can be paired with the diamagnetic counterparts is critical for the assignment. With the data from two tag positions a reliable assignment could be obtained for 60% of the methyl groups and for many of the remaining resonances the number of possible assignments is limited to two or three. With a single tag, reliable assignments can be obtained for methyl groups with large PCS near the tag. It is concluded that assignment of methyl group resonances by paramagnetic tagging can be particularly useful in combination with some additional data, such as from mutagenesis or NOE-based experiments. Approaches to yield the best assignment results with PCS generating tags are discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10858-017-0136-3) contains supplementary material, which is available to authorized users. Springer Netherlands 2017-11-27 2017 /pmc/articles/PMC5736784/ /pubmed/29181729 http://dx.doi.org/10.1007/s10858-017-0136-3 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Lescanne, Mathilde Skinner, Simon P. Blok, Anneloes Timmer, Monika Cerofolini, Linda Fragai, Marco Luchinat, Claudio Ubbink, Marcellus Methyl group assignment using pseudocontact shifts with PARAssign |
title | Methyl group assignment using pseudocontact shifts with PARAssign |
title_full | Methyl group assignment using pseudocontact shifts with PARAssign |
title_fullStr | Methyl group assignment using pseudocontact shifts with PARAssign |
title_full_unstemmed | Methyl group assignment using pseudocontact shifts with PARAssign |
title_short | Methyl group assignment using pseudocontact shifts with PARAssign |
title_sort | methyl group assignment using pseudocontact shifts with parassign |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736784/ https://www.ncbi.nlm.nih.gov/pubmed/29181729 http://dx.doi.org/10.1007/s10858-017-0136-3 |
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