Altering the Energy Landscape of Virus Self-Assembly to Generate Kinetically Trapped Nanoparticles

被引:19
作者
Burns, Kevin [1 ]
Mukherjee, Santanu [1 ]
Keef, Thomas [2 ]
Johnson, Jennifer M. [1 ]
Zlotnick, Adam [1 ,3 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73104 USA
[2] Univ York, Dept Math, York YO10 5DD, N Yorkshire, England
[3] Indiana Univ, Dept Mol & Cellular Biochem, Bloomington, IN 47405 USA
基金
英国工程与自然科学研究理事会;
关键词
CHLOROTIC MOTTLE VIRUS; SPHERICAL VIRUS; COAT PROTEIN; POLYMORPHISM; POLYMER; CAPSIDS;
D O I
10.1021/bm901160b
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
Controlling self-assembly is critical to the advancement of nanotechnology. A rugged or crenated assembly energy surface call redirect assembly off path. By using a defined starting point and in energy Surface made rough by 11 strong association energy, we can impose entirely new assembly paths and products Normally, the coat protein (CP) of the Cowpea Chlorotic Mottle Virus (CCMV)assembles into virus-like 28 nm diameter icosahedral particles Here, we have started with the coat protein trapped in a rod-like structure in complex with DNA When these 17 nm diameter rods tire placed under the same; condition, low pH, that normally leads to assembly of 28 nm diameter particles, we instead obtain 17 nm capsids. The extrusion of all-pentamer capsids from the hexagonal lattice of the rod demonstrates the importance of the starting state for controlled assembly.
引用
收藏
页码:439 / 442
页数:4
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