Moll Wulf-Dieter, Guo Peixuan
Department of Comparative Pathobiology and Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.
J Nanosci Nanotechnol. 2007 Sep;7(9):3257-67. doi: 10.1166/jnn.2007.914.
The bacteriophage phi29 DNA-packaging motor, which translocates and compresses the DNA genome of the phage into its procapsid during virion assembly, involves an essential ring formed by the packaging RNA (pRNA). We attached electron-dense nanoparticles to pRNA by hybridizing a DNA oligonucleotide with a biotin or thiol modification to a 3'-extension of core pRNA, and by coupling streptavidin and biotinylated ferritin, or 5 nm and 10 nm colloidal gold particles, to these modifications. The pRNA conjugates bound to RNA-free phi29 procapsids, and such nanoparticle-bearing procapsids were isolated by ultracentrifugation and analyzed. Electron microscopy showed that ferritin and gold particles were specifically attached to the side of the phi29 procapsid harboring the connector, which is the pRNA binding site. The pRNA-ferritin conjugates bound to procapsids with the same efficiency as pRNA which lacked the high molecular mass label. However, full DNA packaging efficiency in an in vitro phage assembly assay was only reached after the label of such isolated procapsid-pRNA complexes had been released with RNase H. The results provide approaches to assembled ferritin or gold-containing nano-complexes via pRNA mediated assembly.
噬菌体phi29的DNA包装马达在病毒体组装过程中将噬菌体的DNA基因组转运并压缩到其原衣壳中,该过程涉及由包装RNA(pRNA)形成的一个必需环。我们通过将具有生物素或硫醇修饰的DNA寡核苷酸与核心pRNA的3'端延伸杂交,并将链霉亲和素和生物素化铁蛋白或5纳米和10纳米的胶体金颗粒偶联到这些修饰上,从而将电子致密纳米颗粒连接到pRNA上。pRNA缀合物与不含RNA的phi29原衣壳结合,通过超速离心分离出这种带有纳米颗粒的原衣壳并进行分析。电子显微镜显示,铁蛋白和金颗粒特异性地附着在phi29原衣壳带有连接体的一侧,而连接体是pRNA的结合位点。pRNA-铁蛋白缀合物与原衣壳的结合效率与缺乏高分子量标记的pRNA相同。然而,在体外噬菌体组装试验中,只有在用核糖核酸酶H释放这种分离的原衣壳-pRNA复合物的标记后,才能达到完全的DNA包装效率。这些结果提供了通过pRNA介导的组装来组装含 铁蛋白或金的纳米复合物的方法。