A Promiscuous DNA Packaging Machine from Bacteriophage T4

被引:45
作者
Zhang, Zhihong [1 ]
Kottadiel, Vishal I. [1 ]
Vafabakhsh, Reza [2 ]
Dai, Li [1 ]
Chemla, Yann R. [2 ]
Ha, Taekjip [2 ,3 ]
Rao, Venigalla B. [1 ]
机构
[1] Catholic Univ Amer, Dept Biol, Washington, DC 20064 USA
[2] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[3] Howard Hughes Med Inst, Urbana, IL USA
来源
PLOS BIOLOGY | 2011年 / 9卷 / 02期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
PORTAL PROTEIN; FORCE GENERATION; GENETIC-CONTROL; ATPASE ACTIVITY; MOTOR; MORPHOGENESIS; GP17; T4; MECHANISM; TERMINASE;
D O I
10.1371/journal.pbio.1000592
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Complex viruses are assembled from simple protein subunits by sequential and irreversible assembly. During genome packaging in bacteriophages, a powerful molecular motor assembles at the special portal vertex of an empty prohead to initiate packaging. The capsid expands after about 10%-25% of the genome is packaged. When the head is full, the motor cuts the concatemeric DNA and dissociates from the head. Conformational changes, particularly in the portal, are thought to drive these sequential transitions. We found that the phage T4 packaging machine is highly promiscuous, translocating DNA into finished phage heads as well as into proheads. Optical tweezers experiments show that single motors can force exogenous DNA into phage heads at the same rate as into proheads. Single molecule fluorescence measurements demonstrate that phage heads undergo repeated initiations, packaging multiple DNA molecules into the same head. These results suggest that the phage DNA packaging machine has unusual conformational plasticity, powering DNA into an apparently passive capsid receptacle, including the highly stable virus shell, until it is full. These features probably led to the evolution of viral genomes that fit capsid volume, a strikingly common phenomenon in double-stranded DNA viruses, and will potentially allow design of a novel class of nanocapsid delivery vehicles.
引用
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页数:11
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