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-Structure paper
タイトル | Structure of the gene therapy vector, adeno-associated virus with its cell receptor, AAVR. |
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ジャーナル・号・ページ | Elife, Vol. 8, Year 2019 |
掲載日 | 2019年5月22日 |
著者 | Nancy L Meyer / Guiqing Hu / Omar Davulcu / Qing Xie / Alex J Noble / Craig Yoshioka / Drew S Gingerich / Andrew Trzynka / Larry David / Scott M Stagg / Michael Stewart Chapman / |
PubMed 要旨 | Adeno-associated virus (AAV) vectors are preeminent in emerging clinical gene therapies. Generalizing beyond the most tractable genetic diseases will require modulation of cell specificity and immune ...Adeno-associated virus (AAV) vectors are preeminent in emerging clinical gene therapies. Generalizing beyond the most tractable genetic diseases will require modulation of cell specificity and immune neutralization. Interactions of AAV with its cellular receptor, AAVR, are key to understanding cell-entry and trafficking with the rigor needed to engineer tissue-specific vectors. -electron tomography shows ordered binding of part of the flexible receptor to the viral surface, with distal domains in multiple conformations. Regions of the virus and receptor in close physical proximity can be identified by cross-linking/mass spectrometry. -electron microscopy with a two-domain receptor fragment reveals the interactions at 2.4 Å resolution. AAVR binds between AAV's spikes on a plateau that is conserved, except in one clade whose structure is AAVR-incompatible. AAVR's footprint overlaps the epitopes of several neutralizing antibodies, prompting a re-evaluation of neutralization mechanisms. The structure provides a roadmap for experimental probing and manipulation of viral-receptor interactions. |
リンク | Elife / PubMed:31115336 / PubMed Central |
手法 | EM (単粒子) / EM (サブトモグラム平均) / EM (トモグラフィー) |
解像度 | 2.4 - 20.0 Å |
構造データ | EMDB-0553, PDB-6nz0: EMDB-0621: EMDB-0622: EMDB-0623: EMDB-0624: |
化合物 | ChemComp-MG: ChemComp-HOH: |
由来 |
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キーワード | VIRUS / AAV / AAVR / receptor / coreceptor / KIAA0319L / PKD / parvovirus |