Robers Matthew B, Vasta James D, Corona Cesear R, Ohana Rachel Friedman, Hurst Robin, Jhala Manisha A, Comess Kenneth M, Wood Keith V
Promega Corporation, Fitchburg, WI, USA.
Promega Biosciences Incorporated, San Luis Obispo, CA, USA.
Methods Mol Biol. 2019;1888:45-71. doi: 10.1007/978-1-4939-8891-4_3.
Intracellular target affinity and residence time are fundamental aspects of pharmacological mechanism (Lu and Tonge, Curr Opin Chem Biol 14:467-474, 2010). Although various robust biochemical approaches exist to measure these binding characteristics, analysis of compound binding with isolated targets may not accurately reflect engagement in the milieu of living cells. To realize the influence of cellular context, methods are needed that are capable of quantifying affinity and residence time in the presence of the intracellular factors that may impact target engagement. Bioluminescence resonance energy transfer (BRET) offers a solution for intracellular target engagement when quantitative metrics or kinetic analyses are required.
细胞内靶点亲和力和驻留时间是药理机制的基本方面(Lu和Tonge,《化学生物学当前观点》14:467 - 474,2010年)。尽管存在各种可靠的生化方法来测量这些结合特性,但对与分离靶点的化合物结合进行分析可能无法准确反映在活细胞环境中的相互作用。为了了解细胞环境的影响,需要能够在可能影响靶点相互作用的细胞内因子存在的情况下量化亲和力和驻留时间的方法。当需要定量指标或动力学分析时,生物发光共振能量转移(BRET)为细胞内靶点相互作用提供了一种解决方案。