Department of Chemical and Physical Biology, Program on Biomolecular Recognition and Assembly, Centro de Investigaciones Biológicas-CSIC, C/Ramiro de Maeztu 9, 28040 Madrid, Spain.
Chembiochem. 2010 Nov 22;11(17):2347-57. doi: 10.1002/cbic.201000412.
One of the major objectives that bottom-up synthetic biology shares with chemical biology is to engineer extant biological molecules to implement novel functionalities in living systems. Proteins, due to their astonishing structural and functional versatility and to their central roles in the biology of cells, should be cornerstones of synthetic biology. In particular, protein amyloid cross-β assemblies constitute one of the most stable, conceptually simple and universal macromolecular architectures ever found in Nature and thus have enormous potential to be explored. This article focuses on the concepts behind the use of the amyloid cross-β-structural framework as a synthetic biology part, underlining recent basic findings and ideas. The pros and the cons associated with the polymorphism and the cellular toxicity of protein amyloids are also discussed, keeping in mind the possible suitability of these protein assemblies for scaffolding novel orthogonal macromolecular devices in vivo.
与化学生物学一样,自下而上的合成生物学的主要目标之一是设计现有的生物分子,以在生命系统中实现新的功能。由于蛋白质具有惊人的结构和功能多样性,以及在细胞生物学中的核心作用,它们应该是合成生物学的基石。特别是,蛋白质淀粉样纤维交叉-β 组装体构成了自然界中发现的最稳定、概念上最简单和最通用的大分子结构之一,因此具有巨大的探索潜力。本文重点介绍了将淀粉样纤维交叉-β 结构框架用作合成生物学部件的概念,强调了最近的基础发现和想法。还讨论了与蛋白质淀粉样纤维的多态性和细胞毒性相关的优缺点,同时考虑了这些蛋白质组装体在体内构建新型正交大分子器件的可能适用性。