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Searching for the Pareto frontier in multi-objective protein design

机译:在多目标蛋白质设计中寻找帕累托前沿

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摘要

The goal of protein engineering and design is to identify sequences that adopt three-dimensional structures of desired function. Often, this is treated as a single-objective optimization problem, identifying the sequence–structure solution with the lowest computed free energy of folding. However, many design problems are multi-state, multi-specificity, or otherwise require concurrent optimization of multiple objectives. There may be tradeoffs among objectives, where improving one feature requires compromising another. The challenge lies in determining solutions that are part of the Pareto optimal set—designs where no further improvement can be achieved in any of the objectives without degrading one of the others. Pareto optimality problems are found in all areas of study, from economics to engineering to biology, and computational methods have been developed specifically to identify the Pareto frontier. We review progress in multi-objective protein design, the development of Pareto optimization methods, and present a specific case study using multi-objective optimization methods to model the tradeoff between three parameters, stability, specificity, and complexity, of a set of interacting synthetic collagen peptides.
机译:蛋白质工程和设计的目标是鉴定采用所需功能的三维结构的序列。通常,这被视为单目标优化问题,确定具有最低折叠自由能的序列结构解决方案。但是,许多设计问题是多状态,多特异性的,否则需要同时优化多个目标。在目标之间可能需要权衡取舍,其中改进一项功能需要折衷另一项功能。挑战在于确定解决方案,这些解决方案是Pareto最优方案的一部分-在设计中,如果不降低其他任何一个目标,就无法在任何目标上实现进一步的改进。从经济学到工程学到生物学,在所有研究领域中都发现了帕累托最优性问题,并且专门开发了计算方法来识别帕累托前沿。我们回顾了多目标蛋白质设计的进展,帕累托优化方法的发展,并提出了使用多目标优化方法对一组相互作用的合成蛋白的三个参数(稳定性,特异性和复杂性)进行权衡的具体案例研究胶原蛋白肽。

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