Serwer P, Watson R H, Hayes S J
J Virol. 1985 Jul;55(1):232-7. doi: 10.1128/JVI.55.1.232-237.1985.
Like other double-stranded DNA bacteriophages, bacteriophage T3 assembles a DNA-free procapsid that subsequently packages the bacteriophage DNA. By agarose gel electrophoresis, it has been found that the T3 procapsid has a negative electrophoretic mobility (mu) that progressively increases in magnitude by as much as 3% after assembly of the procapsid. This increase is (i) caused by an increase in the solid support-free mu (muo) of the procapsid, not a decrease in its radius, and (ii) not prevented by either genetically or chemically (use of proflavine) blocking DNA packaging. However, inhibition of the formation of high-energy compounds with a mixture of cyanide and fluoride ions does block the time-dependent increase in the magnitude of muo. This increase appears to be accompanied by addition of an unidentified T3 protein to the procapsid.
与其他双链DNA噬菌体一样,噬菌体T3组装一个不含DNA的前衣壳,随后装入噬菌体DNA。通过琼脂糖凝胶电泳发现,T3前衣壳具有负电泳迁移率(μ),在前衣壳组装后其大小会逐渐增加多达3%。这种增加是由于:(i)前衣壳的无固体支持物迁移率(μo)增加,而非其半径减小;(ii)无论是通过基因手段还是化学手段(使用原黄素)阻断DNA包装均不能阻止这种增加。然而,用氰化物和氟离子混合物抑制高能化合物的形成确实会阻断μo大小随时间的增加。这种增加似乎伴随着一种未鉴定的T3蛋白添加到前衣壳中。