4.6 Article

Completion of the AAV Structural Atlas: Serotype Capsid Structures Reveals Clade-Specific Features

期刊

VIRUSES-BASEL
卷 13, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/v13010101

关键词

AAV; serotype; capsid; cryo-EM; genome packaging; gene delivery

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资金

  1. NIH [GM082946, S10 OD018142-01, S10 RR025080-01, U24 GM116788]
  2. University of Florida COM

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This study reports the capsid structures of four additional AAV serotypes, completing the structural atlas of AAV capsids. These structures exhibit AAV capsid features and show classification-specific protein loop conformations. The comprehensive characterization of these structures provides valuable insights for future vector engineering efforts to improve gene delivery success.
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 angstrom 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.

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