Goubin G, Hill M
J Virol. 1979 Feb;29(2):799-804. doi: 10.1128/JVI.29.2.799-804.1979.
Covalently closed circular molecules of viral DNA synthesized in virus-infected cells are composed mainly of monomers sedimenting at 22 to 27S in neutral sucrose gradients. These monomers are detected by annealing with complementary DNA or transfection assay. However, 11% of the infectious circles sediment faster than monomers. There is a peak at 32S which may correspond to dimer molecules. Traces of infectivity (about 3%) found between 32S and 65S suggest the presence of higher oligomers. In alkaline sucrose gradients, covalently closed monomers are found at 64 to 71S. Infectivity of these monomers is reduced by alkali treatment to less than one-tenth, and, perhaps for this reason, no infectious dimers or higher oligomers are observed. It has been shown that upon resedimentation the dimers of 95 can be separated from monomers and detected by hybridization.
在病毒感染细胞中合成的病毒DNA共价闭合环状分子主要由在中性蔗糖梯度中沉降系数为22至27S的单体组成。这些单体通过与互补DNA退火或转染试验来检测。然而,11%的感染性环状分子沉降速度比单体快。在32S处有一个峰值,可能对应于二聚体分子。在32S和65S之间发现的微量感染性(约3%)表明存在更高的寡聚体。在碱性蔗糖梯度中,共价闭合单体出现在64至71S处。这些单体经碱处理后感染性降低至不到十分之一,也许正因如此,未观察到感染性二聚体或更高的寡聚体。已经表明,经再沉降后,95的二聚体可与单体分离并通过杂交检测到。