Department of Biochemistry and Molecular Biology, Center for Structural Biology, McKnight Brain Institute, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Biological Science Imaging Resource, Department of Biological Sciences, Florida State University, Tallahassee, FL 32306, USA.
Viruses. 2021 Jan 13;13(1):101. doi: 10.3390/v13010101.
The capsid structures of most Adeno-associated virus (AAV) serotypes, already assigned to an antigenic clade, have been previously determined. This study reports the remaining capsid structures of AAV7, AAV11, AAV12, and AAV13 determined by cryo-electron microscopy and three-dimensional image reconstruction to 2.96, 2.86, 2.54, and 2.76 Å resolution, respectively. These structures complete the structural atlas of the AAV serotype capsids. AAV7 represents the first clade D capsid structure; AAV11 and AAV12 are of a currently unassigned clade that would include AAV4; and AAV13 represents the first AAV2-AAV3 hybrid clade C capsid structure. These newly determined capsid structures all exhibit the AAV capsid features including 5-fold channels, 3-fold protrusions, 2-fold depressions, and a nucleotide binding pocket with an ordered nucleotide in genome-containing capsids. However, these structures have viral proteins that display clade-specific loop conformations. This structural characterization completes our three-dimensional library of the current AAV serotypes to provide an atlas of surface loop configurations compatible with capsid assembly and amenable for future vector engineering efforts. Derived vectors could improve gene delivery success with respect to specific tissue targeting, transduction efficiency, antigenicity or receptor retargeting.
大多数腺相关病毒 (AAV) 血清型的衣壳结构已经被分配到一个抗原群中,之前已经确定。本研究通过冷冻电镜和三维图像重建,报告了 AAV7、AAV11、AAV12 和 AAV13 的剩余衣壳结构,分辨率分别为 2.96、2.86、2.54 和 2.76Å。这些结构完成了 AAV 血清型衣壳的结构图谱。AAV7 代表第一个 D 群衣壳结构;AAV11 和 AAV12 属于目前未分配的群,其中包括 AAV4;AAV13 代表第一个 AAV2-AAV3 杂交 C 群衣壳结构。这些新确定的衣壳结构都表现出 AAV 衣壳的特征,包括 5 倍通道、3 倍突起、2 倍凹陷和核苷酸结合口袋,其中包含有基因组的衣壳内的有序核苷酸。然而,这些结构的病毒蛋白显示出群特异性的环构象。这种结构特征完成了我们当前 AAV 血清型的三维文库,提供了一个与衣壳组装兼容的表面环构象图谱,适用于未来的载体工程努力。衍生的载体可以提高基因传递的成功率,具体表现在特定组织靶向、转导效率、抗原性或受体重靶向方面。