Computationally designed libraries of fluorescent proteins evaluated by preservation and diversity of function

被引:68
作者
Treynor, Thomas P.
Vizcarra, Christina L.
Nedelcu, Daniel
Mayo, Stephen L.
机构
[1] CALTECH, Howard Hughes Med Inst, Div Biol, Pasadena, CA 91125 USA
[2] CALTECH, Howard Hughes Med Inst, Div Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
GFP; library design; protein design; protein engineering; high-throughput screening;
D O I
10.1073/pnas.0609647103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To determine which of seven library design algorithms best introduces new protein function without destroying it altogether, seven combinatorial libraries of green fluorescent protein variants were designed and synthesized. Each was evaluated by distributions of emission intensity and color compiled from measurements made in vivo. Additional comparisons were made with a library constructed by error-prone PCR. Among the designed libraries, fluorescent function was preserved for the greatest fraction of samples in a library designed by using a structure-based computational method developed and described here. A trend was observed toward greater diversity of color in designed libraries that better preserved fluorescence. Contrary to trends observed among libraries constructed by error-prone PCR, preservation of function was observed to increase with a library's average mutation level among the four libraries designed with structure-based computational methods.
引用
收藏
页码:48 / 53
页数:6
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