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Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)

Aquaporins are a large family of transmembrane channel proteins that facilitate the passive but highly selective transport of water and other small solutes across biological membranes. House dust mite (Dermatophagoides farinae) is the major source of household immunogens, and we have recently report...

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Autores principales: Wang, Li-lei, Yu, Li-li, Zhou, Ying, Wu, Mei-li, Teng, Fei-xiang, Wang, Nan, Cui, Yu-bao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396049/
https://www.ncbi.nlm.nih.gov/pubmed/32775433
http://dx.doi.org/10.1155/2020/6717390
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author Wang, Li-lei
Yu, Li-li
Zhou, Ying
Wu, Mei-li
Teng, Fei-xiang
Wang, Nan
Cui, Yu-bao
author_facet Wang, Li-lei
Yu, Li-li
Zhou, Ying
Wu, Mei-li
Teng, Fei-xiang
Wang, Nan
Cui, Yu-bao
author_sort Wang, Li-lei
collection PubMed
description Aquaporins are a large family of transmembrane channel proteins that facilitate the passive but highly selective transport of water and other small solutes across biological membranes. House dust mite (Dermatophagoides farinae) is the major source of household immunogens, and we have recently reported six cDNA sequence encoding aquaporins from this mite species. To better understand the structure and role of mite aquaporin, we constructed a tertiary structure for DerfAQP1 by homology modeling from the X-ray structure of malaria aquaporin PfAQP (Protein Data Bank code No. 3C02) and conducted molecular dynamics simulation. The simulation arranged seven water molecules in a single file through the pores of the DerfAQP1. Further, two conserved Asn-Pro-Ala motifs were located on Asn203 and Asn77; residues Arg206, Trp57, Met190, Gly200, and Asp207 constituted an extracellular vestibule of the pore; and residues His75, Val80, Ile65, and Ile182 constituted the cytoplasmic portions. The overall free energy profile for water transport through DerfAQP1 revealed an energy barrier of ~2.5 kcal/mol. These results contribute to the understanding of mite physiology and pathology.
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spelling pubmed-73960492020-08-07 Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae) Wang, Li-lei Yu, Li-li Zhou, Ying Wu, Mei-li Teng, Fei-xiang Wang, Nan Cui, Yu-bao Biomed Res Int Research Article Aquaporins are a large family of transmembrane channel proteins that facilitate the passive but highly selective transport of water and other small solutes across biological membranes. House dust mite (Dermatophagoides farinae) is the major source of household immunogens, and we have recently reported six cDNA sequence encoding aquaporins from this mite species. To better understand the structure and role of mite aquaporin, we constructed a tertiary structure for DerfAQP1 by homology modeling from the X-ray structure of malaria aquaporin PfAQP (Protein Data Bank code No. 3C02) and conducted molecular dynamics simulation. The simulation arranged seven water molecules in a single file through the pores of the DerfAQP1. Further, two conserved Asn-Pro-Ala motifs were located on Asn203 and Asn77; residues Arg206, Trp57, Met190, Gly200, and Asp207 constituted an extracellular vestibule of the pore; and residues His75, Val80, Ile65, and Ile182 constituted the cytoplasmic portions. The overall free energy profile for water transport through DerfAQP1 revealed an energy barrier of ~2.5 kcal/mol. These results contribute to the understanding of mite physiology and pathology. Hindawi 2020-07-23 /pmc/articles/PMC7396049/ /pubmed/32775433 http://dx.doi.org/10.1155/2020/6717390 Text en Copyright © 2020 Li-lei Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Li-lei
Yu, Li-li
Zhou, Ying
Wu, Mei-li
Teng, Fei-xiang
Wang, Nan
Cui, Yu-bao
Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)
title Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)
title_full Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)
title_fullStr Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)
title_full_unstemmed Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)
title_short Molecular Dynamics Simulations of Mite Aquaporin DerfAQP1 from the Dust Mite Dermatophagoides farinae (Acariformes: Pyroglyphidae)
title_sort molecular dynamics simulations of mite aquaporin derfaqp1 from the dust mite dermatophagoides farinae (acariformes: pyroglyphidae)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396049/
https://www.ncbi.nlm.nih.gov/pubmed/32775433
http://dx.doi.org/10.1155/2020/6717390
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