Wistuba A, Weger S, Kern A, Kleinschmidt J A
Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Heidelberg, Germany.
J Virol. 1995 Sep;69(9):5311-9. doi: 10.1128/JVI.69.9.5311-5319.1995.
The proteins encoded by the adeno-associated virus type 2 (AAV-2) rep and cap genes obtained during a productive infection of HeLa cells with AAV-2 and adenovirus type 2 were fractionated according to solubility, cellular localization, and sedimentation properties. The majority of Rep and Cap proteins accumulated in the nucleus, where they distributed into a soluble and an insoluble fraction. Analysis of the soluble nuclear fraction of capsid proteins by sucrose density gradients showed that they formed at least three steady-state pools: a monomer pool sedimenting at about 6S, a pool of oligomeric intermediates sedimenting between 10 and 15S, and a broad pool of assembly products with a peak between 60 and 110S, the known sedimentation positions of empty and full capsids. While the soluble nuclear monomer and oligomer pool contained predominantly only two capsid proteins, the 30 to 180S assembly products contained VP1, VP2, and VP3 in a stoichiometry similar to that of purified virions. They probably represent different intermediates in capsid assembly, DNA encapsidation, and capsid maturation. In contrast, the cytoplasmic fraction of capsid proteins showed a pattern of oligomers continuously increasing in size without a defined peak, suggesting that assembly of 60S particles occurs in the nucleus. Soluble nuclear Rep proteins were distributed over the whole sedimentation range, probably as a result of association with AAV DNA. Subfractions of the Rep proteins with defined sedimentation values were obtained in the soluble nuclear and cytoplasmic fractions. We were able to coimmunoprecipitate capsid proteins sedimenting between 60 and 110S with antibodies against Rep proteins, suggesting that they exist in common complexes possibly involved in AAV DNA packaging. Antibodies against the capsid proteins, however, precipitated Rep78 and Rep68 predominantly with a peak around 30S representing a second complex containing Rep and Cap proteins.
在用2型腺相关病毒(AAV - 2)和2型腺病毒对HeLa细胞进行生产性感染期间获得的2型腺相关病毒(AAV - 2)rep和cap基因所编码的蛋白质,根据其溶解性、细胞定位和沉降特性进行了分级分离。大多数Rep和Cap蛋白积聚在细胞核中,在那里它们分布到可溶和不可溶部分。通过蔗糖密度梯度对衣壳蛋白的可溶性核部分进行分析表明,它们形成了至少三个稳态池:一个沉降系数约为6S的单体池,一个沉降系数在10至15S之间的寡聚中间体池,以及一个沉降系数峰值在60至110S之间的宽泛的组装产物池,这是已知的空衣壳和完整衣壳的沉降位置。虽然可溶性核单体和寡聚体池中主要仅含有两种衣壳蛋白,但沉降系数为30至180S的组装产物中VP1、VP2和VP3的化学计量比与纯化病毒粒子相似。它们可能代表衣壳组装、DNA包装和衣壳成熟过程中的不同中间体。相比之下,衣壳蛋白的细胞质部分显示出寡聚体大小持续增加且无明确峰值的模式,这表明60S颗粒的组装发生在细胞核中。可溶性核Rep蛋白分布在整个沉降范围内,这可能是与AAV DNA结合的结果。在可溶性核部分和细胞质部分中获得了具有确定沉降值的Rep蛋白亚组分。我们能够用针对Rep蛋白的抗体共免疫沉淀沉降系数在60至110S之间的衣壳蛋白,这表明它们存在于可能参与AAV DNA包装的共同复合物中。然而,针对衣壳蛋白的抗体主要沉淀出沉降系数约为30S的Rep78和Rep68,代表含有Rep和Cap蛋白的第二种复合物。