费斯特共振能量转移
荧光
药物发现
生物物理学
材料科学
计算生物学
化学
纳米技术
组合化学
物理
生物化学
生物
量子力学
作者
Erik K. Larsen,Maria Abreu-Blanco,Dana Rabara,Andrew Stephen
出处
期刊:Methods in molecular biology
日期:2024-01-01
卷期号:: 159-175
标识
DOI:10.1007/978-1-0716-3822-4_12
摘要
Homogenous time-resolved FRET (HTRF) assays have become one of the most popular tools for pharmaceutical drug screening efforts over the last two decades. Large Stokes shifts and long fluorescent lifetimes of lanthanide chelates lead to robust signal to noise, as well as decreased false positive rates compared to traditional assay techniques. In this chapter, we describe an HTRF protein-protein interaction (PPI) assay for the KRAS4b G-domain in the GppNHp-bound state and the RAF-1-RBD currently used for drug screens. Application of this assay contributes to the identification of lead compounds targeting the GTP-bound active state of K-RAS.
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