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Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution

Adeno-associated virus is the leading viral vector for gene therapy. AAV-DJ is a recombinant variant developed for tropism to the liver. The AAV-DJ structure has been determined to 1.56 Å resolution through cryo-electron microscopy (cryo-EM). Only apoferritin is reported in preprints at 1.6 Å or hig...

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Autores principales: Xie, Qing, Yoshioka, Craig K., Chapman, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589773/
https://www.ncbi.nlm.nih.gov/pubmed/33092282
http://dx.doi.org/10.3390/v12101194
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author Xie, Qing
Yoshioka, Craig K.
Chapman, Michael S.
author_facet Xie, Qing
Yoshioka, Craig K.
Chapman, Michael S.
author_sort Xie, Qing
collection PubMed
description Adeno-associated virus is the leading viral vector for gene therapy. AAV-DJ is a recombinant variant developed for tropism to the liver. The AAV-DJ structure has been determined to 1.56 Å resolution through cryo-electron microscopy (cryo-EM). Only apoferritin is reported in preprints at 1.6 Å or higher resolution, and AAV-DJ nearly matches the highest resolutions ever attained through X-ray diffraction of virus crystals. However, cryo-EM has the advantage that most of the hydrogens are clear, improving the accuracy of atomic refinement, and removing ambiguity in hydrogen bond identification. Outside of secondary structures where hydrogen bonding was predictable a priori, the networks of hydrogen bonds coming from direct observation of hydrogens and acceptor atoms are quite different from those inferred even at 2.8 Å resolution. The implications for understanding viral assembly mean that cryo-EM will likely become the favored approach for high resolution structural virology.
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spelling pubmed-75897732020-10-29 Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution Xie, Qing Yoshioka, Craig K. Chapman, Michael S. Viruses Article Adeno-associated virus is the leading viral vector for gene therapy. AAV-DJ is a recombinant variant developed for tropism to the liver. The AAV-DJ structure has been determined to 1.56 Å resolution through cryo-electron microscopy (cryo-EM). Only apoferritin is reported in preprints at 1.6 Å or higher resolution, and AAV-DJ nearly matches the highest resolutions ever attained through X-ray diffraction of virus crystals. However, cryo-EM has the advantage that most of the hydrogens are clear, improving the accuracy of atomic refinement, and removing ambiguity in hydrogen bond identification. Outside of secondary structures where hydrogen bonding was predictable a priori, the networks of hydrogen bonds coming from direct observation of hydrogens and acceptor atoms are quite different from those inferred even at 2.8 Å resolution. The implications for understanding viral assembly mean that cryo-EM will likely become the favored approach for high resolution structural virology. MDPI 2020-10-20 /pmc/articles/PMC7589773/ /pubmed/33092282 http://dx.doi.org/10.3390/v12101194 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xie, Qing
Yoshioka, Craig K.
Chapman, Michael S.
Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution
title Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution
title_full Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution
title_fullStr Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution
title_full_unstemmed Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution
title_short Adeno-Associated Virus (AAV-DJ)—Cryo-EM Structure at 1.56 Å Resolution
title_sort adeno-associated virus (aav-dj)—cryo-em structure at 1.56 å resolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589773/
https://www.ncbi.nlm.nih.gov/pubmed/33092282
http://dx.doi.org/10.3390/v12101194
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