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柯萨奇病毒-腺病毒受体蛋白可作为A、C、D、E和F亚组腺病毒血清型的细胞附着蛋白发挥作用。

The coxsackievirus-adenovirus receptor protein can function as a cellular attachment protein for adenovirus serotypes from subgroups A, C, D, E, and F.

作者信息

Roelvink P W, Lizonova A, Lee J G, Li Y, Bergelson J M, Finberg R W, Brough D E, Kovesdi I, Wickham T J

机构信息

GenVec Inc., Rockville, Maryland 20852, USA.

出版信息

J Virol. 1998 Oct;72(10):7909-15. doi: 10.1128/JVI.72.10.7909-7915.1998.

Abstract

Attachment of an adenovirus (Ad) to a cell is mediated by the capsid fiber protein. To date, only the cellular fiber receptor for subgroup C serotypes 2 and 5, the so-called coxsackievirus-adenovirus receptor (CAR) protein, has been identified and cloned. Previous data suggested that the fiber of the subgroup D serotype Ad9 also recognizes CAR, since Ad9 and Ad2 fiber knobs cross-blocked each other's cellular binding. Recombinant fiber knobs and 3H-labeled Ad virions from serotypes representing all six subgroups (A to F) were used to determine whether the knobs cross-blocked the binding of virions from different subgroups. With the exception of subgroup B, all subgroup representatives cross-competed, suggesting that they use CAR as a cellular fiber receptor as well. This result was confirmed by showing that CAR, produced in a soluble recombinant form (sCAR), bound to nitrocellulose-immobilized virions from the different subgroups except subgroup B. Similar results were found for blotted fiber knob proteins. The subgroup F virus Ad41 has both short and long fibers, but only the long fiber bound sCAR. The sCAR protein blocked the attachment of all virus serotypes that bound CAR. Moreover, CHO cells expressing human CAR, in contrast to untransformed CHO cells, all specifically bound the sCAR-binding serotypes. We conclude therefore that Ad serotypes from subgroups A, C, D, E, and F all use CAR as a cellular fiber receptor.

摘要

腺病毒(Ad)与细胞的附着是由衣壳纤维蛋白介导的。迄今为止,仅鉴定并克隆了C亚组2型和5型血清型的细胞纤维受体,即所谓的柯萨奇病毒-腺病毒受体(CAR)蛋白。先前的数据表明,D亚组血清型Ad9的纤维也识别CAR,因为Ad9和Ad2纤维钮相互交叉阻断了彼此的细胞结合。使用来自代表所有六个亚组(A至F)的血清型的重组纤维钮和3H标记的Ad病毒粒子来确定这些钮是否交叉阻断来自不同亚组的病毒粒子的结合。除了B亚组外,所有亚组代表都存在交叉竞争,这表明它们也使用CAR作为细胞纤维受体。通过显示以可溶性重组形式(sCAR)产生的CAR与除B亚组外的不同亚组的硝酸纤维素固定的病毒粒子结合,证实了这一结果。对于印迹的纤维钮蛋白也发现了类似的结果。F亚组病毒Ad41具有短纤维和长纤维,但只有长纤维与sCAR结合。sCAR蛋白阻断了所有与CAR结合的病毒血清型的附着。此外,与未转化的CHO细胞相比,表达人CAR的CHO细胞均特异性结合sCAR结合血清型。因此,我们得出结论,A、C、D、E和F亚组的Ad血清型均使用CAR作为细胞纤维受体。

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