Oh Kenneth J, Cash Kevin J, Plaxco Kevin W
Department of Chemistry and Biochemistry, University of California, Santa Barbara, Santa Barbara, California 93106, USA.
Chemistry. 2009;15(10):2244-51. doi: 10.1002/chem.200701748.
Many polypeptides and small proteins can be readily engineered such that they only fold upon binding a specific target ligand. This approach couples target recognition with a considerable change in polymer structure and dynamics. Recent years have seen the development of a number of biosensors that couple these large changes to readily measurable optical (fluorescent) outputs. These sensors afford the detection of a wide variety of macromolecular targets including proteins, polypeptides, and nucleic acids. Here we describe the design of such biosensors, from the first iterations as protein engineering experiments, to the development of biosensors targeting a range of protein and nucleic acid targets.
许多多肽和小蛋白可以很容易地进行工程改造,使其仅在结合特定靶标配体时才折叠。这种方法将靶标识别与聚合物结构和动力学的显著变化结合起来。近年来,已经开发出了许多生物传感器,这些生物传感器将这些大的变化与易于测量的光学(荧光)输出耦合起来。这些传感器能够检测多种大分子靶标,包括蛋白质、多肽和核酸。在这里,我们描述了此类生物传感器的设计,从作为蛋白质工程实验的最初迭代,到针对一系列蛋白质和核酸靶标的生物传感器的开发。