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腺相关病毒 (AAV-DJ)-冷冻电镜结构解析至 1.56 Å 分辨率。

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

机构信息

Department of Biochemistry & Molecular Biology, Oregon Health & Science University, Portland, OR 97239, USA.

Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.

出版信息

Viruses. 2020 Oct 20;12(10):1194. doi: 10.3390/v12101194.

Abstract

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.

摘要

腺相关病毒是基因治疗的主要病毒载体。AAV-DJ 是为了靶向肝脏而开发的重组变体。通过冷冻电镜(cryo-EM)确定了 AAV-DJ 的结构分辨率为 1.56Å。在预印本中,只有脱铁铁蛋白的分辨率为 1.6Å 或更高,而 AAV-DJ 几乎与通过病毒晶体 X 射线衍射获得的最高分辨率相匹配。然而,冷冻电镜具有大多数氢原子清晰的优势,这提高了原子精修的准确性,并消除了氢键识别中的歧义。在二级结构中,氢键是可以先验预测的,而来自直接观察氢原子和受体原子的氢键网络与即使在 2.8Å 分辨率下推断的网络有很大的不同。这对于理解病毒组装的意义意味着,冷冻电镜可能成为高分辨率结构病毒学的首选方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46bd/7589773/c9759e248aa0/viruses-12-01194-g001.jpg

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