Marshall Shannon A, Lazar Greg A, Chirino Arthur J, Desjarlais John R
Xencor, 111 W. Lemon Avenue, Monrovia, CA 91016, USA.
Drug Discov Today. 2003 Mar 1;8(5):212-21. doi: 10.1016/s1359-6446(03)02610-2.
An increasing number of engineered protein therapeutics are currently being developed, tested in clinical trials and marketed for use. Many of these proteins arose out of hit-and-miss efforts to discover specific mutations, fusion partners or chemical modifications that confer desired properties. Through these efforts, several useful strategies have emerged for rational optimization of therapeutic candidates. The controlled manipulation of the physical, chemical and biological properties of proteins enabled by structure-based simulation is now being used to refine established rational engineering approaches and to advance new strategies. These methods provide clear, hypothesis-driven routes to solve problems that plague many proteins and to create novel mechanisms of action. We anticipate that rational protein engineering will shape the field of protein therapeutics dramatically by improving existing products and enabling the development of novel therapeutic agents.
目前,越来越多的工程蛋白疗法正在研发、进行临床试验并上市使用。这些蛋白中的许多都是通过偶然发现特定突变、融合伙伴或化学修饰以赋予所需特性的尝试而产生的。通过这些努力,出现了几种用于合理优化候选治疗药物的有用策略。基于结构的模拟使对蛋白质的物理、化学和生物学特性进行可控操作,现在正被用于完善既定的合理工程方法并推进新策略。这些方法提供了清晰的、基于假设的途径,以解决困扰许多蛋白质的问题并创造新的作用机制。我们预计,合理的蛋白质工程将通过改进现有产品并推动新型治疗药物的开发,极大地塑造蛋白质治疗领域。