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
相关论文
共 39 条
  • [11] Energy functions for protein design
    Gordon, DB
    Marshall, SA
    Mayo, SL
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 1999, 9 (04) : 509 - 513
  • [12] Exact rotamer optimization for protein design
    Gordon, DB
    Hom, GK
    Mayo, SL
    Pierce, NA
    [J]. JOURNAL OF COMPUTATIONAL CHEMISTRY, 2003, 24 (02) : 232 - 243
  • [13] Combining computational and experimental screening for rapid optimization of protein properties
    Hayes, RJ
    Bentzien, J
    Ary, ML
    Hwang, MY
    Jacinto, JM
    Vielmetter, J
    Kundu, A
    Dahiyat, BI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (25) : 15926 - 15931
  • [14] IMPROVED GREEN FLUORESCENCE
    HEIM, R
    CUBITT, AB
    TSIEN, RY
    [J]. NATURE, 1995, 373 (6516) : 663 - 664
  • [15] Engineering green fluorescent protein for improved brightness, longer wavelengths and fluorescence resonance energy transfer
    Hein, R
    Tsien, RY
    [J]. CURRENT BIOLOGY, 1996, 6 (02) : 178 - 182
  • [16] General method for sequence-independent site-directed chimeragenesis
    Hiraga, K
    Arnold, FH
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2003, 330 (02) : 287 - 296
  • [17] Creating randomized amino acid libraries with the QuikChange® Multi Site-Directed Mutagenesis Kit
    Hogrefe, HH
    Cline, J
    Youngblood, GL
    Allen, RM
    [J]. BIOTECHNIQUES, 2002, 33 (05) : 1158 - +
  • [18] Selecting and screening recombinant antibody libraries
    Hoogenboom, HR
    [J]. NATURE BIOTECHNOLOGY, 2005, 23 (09) : 1105 - 1116
  • [19] Local complexity of amino acid interactions in a protein core
    Jain, RK
    Ranganathan, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (01) : 111 - 116
  • [20] Design of a novel globular protein fold with atomic-level accuracy
    Kuhlman, B
    Dantas, G
    Ireton, GC
    Varani, G
    Stoddard, BL
    Baker, D
    [J]. SCIENCE, 2003, 302 (5649) : 1364 - 1368