Department of Biochemistry, The University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.
J Mol Biol. 2010 Mar 26;397(2):361-74. doi: 10.1016/j.jmb.2010.01.058. Epub 2010 Feb 1.
Evidence that in vivo bacteriophage T3 DNA packaging includes capsid hyper-expansion that is triggered by lengthening of incompletely packaged DNA (ipDNA) is presented here. This evidence includes observation that some of the longer ipDNAs in T3-infected cells are packaged in ipDNA-containing capsids with hyper-expanded outer shells (HE ipDNA-capsids). In addition, artificially induced hyper-expansion is observed for the outer shell of a DNA-free capsid. Detection and characterization of HE ipDNA-capsids are based on two-dimensional, non-denaturing agarose gel electrophoresis, followed by structure determination with electron microscopy and protein identification with SDS-PAGE/mass spectrometry. After expulsion from HE ipDNA-capsids, ipDNA forms sharp bands during gel electrophoresis. The following hypotheses are presented: (1) T3 has evolved feedback-initiated, ATP-driven capsid contraction/hyper-expansion cycles that accelerate DNA packaging when packaging is slowed by increase in the packaging-resisting force of the ipDNA and (2) each gel electrophoretic ipDNA band reflects a contraction/hyper-expansion cycle.
现有的证据表明,噬菌体 T3 体内 DNA 包装包括衣壳超扩张,这是由不完全包装的 DNA(ipDNA)的延长触发的。这些证据包括观察到在 T3 感染的细胞中,一些较长的 ipDNA 被包装在含有超扩张外壳的 ipDNA 衣壳中(HE ipDNA-衣壳)。此外,还观察到人工诱导的无 DNA 衣壳的超扩张。HE ipDNA-衣壳的检测和表征基于二维、非变性琼脂糖凝胶电泳,随后通过电子显微镜进行结构测定和 SDS-PAGE/质谱法进行蛋白质鉴定。从 HE ipDNA-衣壳中排出后,ipDNA 在凝胶电泳中形成锐利的条带。提出了以下假设:(1)T3 已经进化出反馈启动的、ATP 驱动的衣壳收缩/超扩张循环,当 ipDNA 的包装阻力增加导致包装速度减慢时,这些循环可以加速 DNA 包装;(2)每个凝胶电泳 ipDNA 条带反映一个收缩/超扩张循环。