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Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6
Lipocalins represent the most important protein family of the mammalian respiratory allergens. Four of the seven named dog allergens are lipocalins: Can f 1, Can f 2, Can f 4, and Can f 6. We present the structure of Can f 6 along with data on the biophysical and biological activity of this protein...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746357/ https://www.ncbi.nlm.nih.gov/pubmed/31525203 http://dx.doi.org/10.1371/journal.pone.0213052 |
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author | Clayton, Gina M. White, Janice Lee, Schuyler Kappler, John W. Chan, Sanny K. |
author_facet | Clayton, Gina M. White, Janice Lee, Schuyler Kappler, John W. Chan, Sanny K. |
author_sort | Clayton, Gina M. |
collection | PubMed |
description | Lipocalins represent the most important protein family of the mammalian respiratory allergens. Four of the seven named dog allergens are lipocalins: Can f 1, Can f 2, Can f 4, and Can f 6. We present the structure of Can f 6 along with data on the biophysical and biological activity of this protein in comparison with other animal lipocalins. The Can f 6 structure displays the classic lipocalin calyx-shaped ligand binding cavity within a central β-barrel similar to other lipocalins. Despite low sequence identity between the different dog lipocalin proteins, there is a high degree of structural similarity. On the other hand, Can f 6 has a similar primary sequence to cat, horse, mouse lipocalins as well as a structure that may underlie their cross reactivity. Interestingly, the entrance to the ligand binding pocket is capped by a His instead of the usually seen Tyr that may help select its natural ligand binding partner. Our highly pure recombinant Can f 6 is able to bind to human IgE (hIgE) demonstrating biological antigenicity. |
format | Online Article Text |
id | pubmed-6746357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67463572019-09-27 Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 Clayton, Gina M. White, Janice Lee, Schuyler Kappler, John W. Chan, Sanny K. PLoS One Research Article Lipocalins represent the most important protein family of the mammalian respiratory allergens. Four of the seven named dog allergens are lipocalins: Can f 1, Can f 2, Can f 4, and Can f 6. We present the structure of Can f 6 along with data on the biophysical and biological activity of this protein in comparison with other animal lipocalins. The Can f 6 structure displays the classic lipocalin calyx-shaped ligand binding cavity within a central β-barrel similar to other lipocalins. Despite low sequence identity between the different dog lipocalin proteins, there is a high degree of structural similarity. On the other hand, Can f 6 has a similar primary sequence to cat, horse, mouse lipocalins as well as a structure that may underlie their cross reactivity. Interestingly, the entrance to the ligand binding pocket is capped by a His instead of the usually seen Tyr that may help select its natural ligand binding partner. Our highly pure recombinant Can f 6 is able to bind to human IgE (hIgE) demonstrating biological antigenicity. Public Library of Science 2019-09-16 /pmc/articles/PMC6746357/ /pubmed/31525203 http://dx.doi.org/10.1371/journal.pone.0213052 Text en © 2019 Clayton 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 Clayton, Gina M. White, Janice Lee, Schuyler Kappler, John W. Chan, Sanny K. Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 |
title | Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 |
title_full | Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 |
title_fullStr | Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 |
title_full_unstemmed | Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 |
title_short | Structural characteristics of lipocalin allergens: Crystal structure of the immunogenic dog allergen Can f 6 |
title_sort | structural characteristics of lipocalin allergens: crystal structure of the immunogenic dog allergen can f 6 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746357/ https://www.ncbi.nlm.nih.gov/pubmed/31525203 http://dx.doi.org/10.1371/journal.pone.0213052 |
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