Torres Francisco E, Kuhn Peter, De Bruyker Dirk, Bell Alan G, Wolkin Michal V, Peeters Eric, Williamson James R, Anderson Gregory B, Schmitz Gregory P, Recht Michael I, Schweizer Sandra, Scott Lincoln G, Ho Jackson H, Elrod Scott A, Schultz Peter G, Lerner Richard A, Bruce Richard H
Scripps-PARC Institute for Advanced Biomedical Sciences, Palo Alto Research Center, 3333 Coyote Hill Road, Palo Alto, CA 94304, USA.
Proc Natl Acad Sci U S A. 2004 Jun 29;101(26):9517-22. doi: 10.1073/pnas.0403573101. Epub 2004 Jun 21.
We report the fabrication of enthalpy arrays and their use to detect molecular interactions, including protein-ligand binding, enzymatic turnover, and mitochondrial respiration. Enthalpy arrays provide a universal assay methodology with no need for specific assay development such as fluorescent labeling or immobilization of reagents, which can adversely affect the interaction. Microscale technology enables the fabrication of 96-detector enthalpy arrays on large substrates. The reduction in scale results in large decreases in both the sample quantity and the measurement time compared with conventional microcalorimetry. We demonstrate the utility of the enthalpy arrays by showing measurements for two protein-ligand binding interactions (RNase A + cytidine 2'-monophosphate and streptavidin + biotin), phosphorylation of glucose by hexokinase, and respiration of mitochondria in the presence of 2,4-dinitrophenol uncoupler.
我们报告了焓阵列的制备及其用于检测分子相互作用的情况,包括蛋白质-配体结合、酶促周转和线粒体呼吸。焓阵列提供了一种通用的检测方法,无需进行特定的检测开发,如荧光标记或试剂固定,而这些可能会对相互作用产生不利影响。微尺度技术能够在大尺寸基板上制备具有96个探测器的焓阵列。与传统微量热法相比,规模的缩小导致样品量和测量时间大幅减少。我们通过展示两种蛋白质-配体结合相互作用(核糖核酸酶A+2'-单磷酸胞苷和抗生物素蛋白+生物素)、己糖激酶催化葡萄糖磷酸化以及在存在2,4-二硝基苯酚解偶联剂的情况下线粒体呼吸的测量结果,证明了焓阵列的实用性。