首页> 外文期刊>Acta crystallographica. Section D, Structural biology >Cryo‐EM structure of adeno‐associated virus 4 at 2.2?? resolution
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Cryo‐EM structure of adeno‐associated virus 4 at 2.2?? resolution

机译:腺相关病毒 4 在 2.2??分辨率

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Adeno‐associated virus (AAV) is the vector of choice for several approved gene‐therapy treatments and is the basis for many ongoing clinical trials. Various strains of AAV exist (referred to as serotypes), each with their own transfection characteristics. Here, a high‐resolution cryo‐electron microscopy structure (2.2??) of AAV serotype 4 (AAV4) is presented. The receptor responsible for transduction of the AAV4 clade of AAV viruses (including AAV11, AAV12 and AAVrh32.33) is unknown. Other AAVs interact with the same cell receptor, adeno‐associated virus receptor (AAVR), in one of two different ways. AAV5‐like viruses interact exclusively with the polycystic kidney disease‐like 1 (PKD1) domain of AAVR, while most other AAVs interact primarily with the PKD2 domain. A comparison of the present AAV4 structure with prior corresponding structures of AAV5, AAV2 and AAV1 in complex with AAVR provides a foundation for understanding why the AAV4‐like clade is unable to interact with either PKD1 or PKD2 of AAVR. The conformation of the AAV4 capsid in variable regions I, III, IV and V on the viral surface appears to be sufficiently different from AAV2 to ablate binding with PKD2. Differences between AAV4 and AAV5 in variable region VII appear to be sufficient to exclude binding with PKD1.
机译:腺相关病毒(AAV)应承担的向量选择几个通过基因疗法治疗是许多正在进行的基础临床试验(称为血清型),每个国家都有他们自己的转染特点。低温高分辨率的电子显微镜AAV血清型的结构(2.2 ?)4 (AAV4)提出了。转导的AAV4 AAV病毒的进化枝(包括AAV11 AAV12和AAVrh32.33)未知的。受体,腺相关病毒受体应承担(AAVR),在两种不同的方式之一。只与多囊肾交互疾病类1 (PKD1) AAVR领域,虽然大多数其他装甲防护主要是与PKD2交互域。前结构与相应的结构AAV5, AAV2 AAV1与AAVR提供复杂理解为什么AAV4检测的基础进化枝无法与PKD1或交互PKD2 AAVR。变量地区,III, IV和V的病毒表面似乎相当不同与PKD2 AAV2切除绑定。AAV4与AAV5变量地区七世似乎足以排除绑定PKD1。

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