Coping With Complexity: Machine Learning Optimization of Cell-Free Protein Synthesis

被引:41
|
作者
Caschera, Filippo [1 ,2 ]
Bedau, Mark A. [1 ,3 ]
Buchanan, Andrew [1 ]
Cawse, James [1 ,4 ]
de Lucrezia, Davide [5 ,6 ]
Gazzola, Gianluca [1 ,7 ]
Hanczyc, Martin M. [1 ,2 ]
Packard, Norman H. [1 ,5 ,8 ]
机构
[1] ProtoLife Inc, San Francisco, CA 94104 USA
[2] Univ So Denmark, Dept Chem & Phys, Odense, Denmark
[3] Reed Coll, Portland, OR 97202 USA
[4] Cawse & Effect, Pittsfield, MA USA
[5] European Ctr Living Technol, Venice, Italy
[6] Explora Srl, Rome, Italy
[7] Rutgers State Univ, Rutgers Ctr Operat Res, New Brunswick, NJ 08903 USA
[8] Santa Fe Inst, Santa Fe, NM 87501 USA
关键词
design of experiments; protein expression; complexity; optimization; HIGH-THROUGHPUT; SYNTHESIS SYSTEM; ATP REGENERATION; RNA-POLYMERASE; MESSENGER-RNA; EXPRESSION; TRANSLATION; COLI; DISCOVERY; GLUCOSE;
D O I
10.1002/bit.23178
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biological systems contain complex metabolic pathways with many nonlinearities and synergies that make them difficult to predict from first principles. Protein synthesis is a canonical example of such a pathway. Here we show how cell-free protein synthesis may be improved through a series of iterated high-throughput experiments guided by a machine-learning algorithm implementing a form of evolutionary design of experiments (Evo-DoE). The algorithm predicts fruitful experiments from statistical models of the previous experimental results, combined with stochastic exploration of the experimental space. The desired experimental response, or evolutionary fitness, was defined as the yield of the target product, and new experimental conditions were discovered to have similar to 350% greater yield than the standard. An analysis of the best experimental conditions discovered indicates that there are two distinct classes of kinetics, thus showing how our evolutionary design of experiments is capable of significant innovation, as well as gradual improvement. Biotechnol. Bioeng. 2011; 108: 2218-2228. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:2218 / 2228
页数:11
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