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Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints
Structural restrictions are present even in the most sequence diverse portions of antibodies, the complementary determining region (CDR) loops. Previous studies identified robust rules that define canonical structures for five of the six CDR loops, however the heavy chain CDR 3 (HCDR3) defies standa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868311/ https://www.ncbi.nlm.nih.gov/pubmed/27182833 http://dx.doi.org/10.1371/journal.pone.0154811 |
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author | Finn, Jessica A. Koehler Leman, Julia Willis, Jordan R. Cisneros, Alberto Crowe, James E. Meiler, Jens |
author_facet | Finn, Jessica A. Koehler Leman, Julia Willis, Jordan R. Cisneros, Alberto Crowe, James E. Meiler, Jens |
author_sort | Finn, Jessica A. |
collection | PubMed |
description | Structural restrictions are present even in the most sequence diverse portions of antibodies, the complementary determining region (CDR) loops. Previous studies identified robust rules that define canonical structures for five of the six CDR loops, however the heavy chain CDR 3 (HCDR3) defies standard classification attempts. The HCDR3 loop can be subdivided into two domains referred to as the “torso” and the “head” domains and two major families of canonical torso structures have been identified; the more prevalent “bulged” and less frequent “non-bulged” torsos. In the present study, we found that Rosetta loop modeling of 28 benchmark bulged HCDR3 loops is improved with knowledge-based structural restraints developed from available antibody crystal structures in the PDB. These restraints restrict the sampling space Rosetta searches in the torso domain, limiting the φ and ψ angles of these residues to conformations that have been experimentally observed. The application of these restraints in Rosetta result in more native-like structure sampling and improved score-based differentiation of native-like HCDR3 models, significantly improving our ability to model antibody HCDR3 loops. |
format | Online Article Text |
id | pubmed-4868311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48683112016-05-26 Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints Finn, Jessica A. Koehler Leman, Julia Willis, Jordan R. Cisneros, Alberto Crowe, James E. Meiler, Jens PLoS One Research Article Structural restrictions are present even in the most sequence diverse portions of antibodies, the complementary determining region (CDR) loops. Previous studies identified robust rules that define canonical structures for five of the six CDR loops, however the heavy chain CDR 3 (HCDR3) defies standard classification attempts. The HCDR3 loop can be subdivided into two domains referred to as the “torso” and the “head” domains and two major families of canonical torso structures have been identified; the more prevalent “bulged” and less frequent “non-bulged” torsos. In the present study, we found that Rosetta loop modeling of 28 benchmark bulged HCDR3 loops is improved with knowledge-based structural restraints developed from available antibody crystal structures in the PDB. These restraints restrict the sampling space Rosetta searches in the torso domain, limiting the φ and ψ angles of these residues to conformations that have been experimentally observed. The application of these restraints in Rosetta result in more native-like structure sampling and improved score-based differentiation of native-like HCDR3 models, significantly improving our ability to model antibody HCDR3 loops. Public Library of Science 2016-05-16 /pmc/articles/PMC4868311/ /pubmed/27182833 http://dx.doi.org/10.1371/journal.pone.0154811 Text en © 2016 Finn et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Finn, Jessica A. Koehler Leman, Julia Willis, Jordan R. Cisneros, Alberto Crowe, James E. Meiler, Jens Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints |
title | Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints |
title_full | Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints |
title_fullStr | Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints |
title_full_unstemmed | Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints |
title_short | Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints |
title_sort | improving loop modeling of the antibody complementarity-determining region 3 using knowledge-based restraints |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868311/ https://www.ncbi.nlm.nih.gov/pubmed/27182833 http://dx.doi.org/10.1371/journal.pone.0154811 |
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