Russell W C, Precious B
J Gen Virol. 1982 Nov;63 (Pt 1):69-79. doi: 10.1099/0022-1317-63-1-69.
The ability of adenovirus structural polypeptides to bind nucleic acids was assessed by separating the polypeptides on SDS-polyacrylamide gels, transferring them electrophoretically to nitrocellulose and probing with 32P-labelled nucleic acids. Polypeptides IVa2, V, VI and VII, as well as trace amounts of pVII and a polypeptide of apparent mol. wt. 40 X 10(3) were able to bind label under these conditions. Labelling was also detected with a smaller polypeptide, possibly related to the cleavage products of pVII and/or pVI. The binding of DNA to polypeptide VI appeared to be more sensitive to detergents than the others. No sequence specificity could be detected in the DNA binding.
通过在SDS-聚丙烯酰胺凝胶上分离腺病毒结构多肽,将其电泳转移至硝酸纤维素膜上并用32P标记的核酸进行探测,来评估腺病毒结构多肽与核酸结合的能力。在这些条件下,多肽IVa2、V、VI和VII,以及痕量的pVII和一种表观分子量为40×10³的多肽能够结合标记物。还检测到一种较小的多肽带有标记,它可能与pVII和/或pVI的裂解产物有关。与其他多肽相比,DNA与多肽VI的结合似乎对去污剂更敏感。在DNA结合中未检测到序列特异性。