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Mechanism of Termination of Bacteriophage DNA Packaging Investigated with Optical Tweezers
被引:0
|作者:
delToro, Damian J.
[1
]
Smith, Douglas E.
[1
]
机构:
[1] Univ Calif San Diego, Dept Phys, La Jolla, CA 92093 USA
来源:
关键词:
Optical tweezers;
Lambda;
terminase;
viral packaging;
dual trap;
COHESIVE END SITE;
PHAGE-LAMBDA;
PORTAL PROTEIN;
COSQ;
CHROMOSOME;
MUTATIONS;
NICKING;
SIGNAL;
D O I:
10.1117/12.930425
中图分类号:
O43 [光学];
学科分类号:
070207 ;
0803 ;
摘要:
The genomes of many dsDNA viruses are replicated by a mechanism that produces a long concatemer of multiple genomes. These viruses utilize multifunctional molecular motor complexes referred to as "terminases" that can excise a unit genome length of DNA and package it into preformed viral shells. Remarkably, the terminase motor can initiate packaging at the appropriate start point, translocate DNA, sense when a sufficient length has been packaged, and then switch into a mode where it arrests and cleaves the DNA to release a filled virus particle. We have recently developed an improved method to measure single phage lambda DNA packaging using dual-trap optical tweezers and pre-stalled motor-DNA-procapsid complexes. We are applying this method to test proposed mechanisms for the sensor that triggers termination; specifically a velocity-monitor model vs. energy-monitor model vs. capsid-filling monitor model.
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