Center for Plant Molecular Biology (ZMBP), University of Tübingen, Tübingen, Germany.
Department of Plant Molecular Biology (DBMV), University of Lausanne, Lausanne, Switzerland.
Methods Mol Biol. 2024;2731:265-278. doi: 10.1007/978-1-0716-3511-7_20.
The quantitative and qualitative biochemical description of molecular interactions is fundamental to the study of ligand/receptor pairs and their structure/function relationships. Bioactive peptides often are active at (sub-)nanomolar concentrations, indicating they have a high affinity for their sites of action, notably binding sites on receptors. Since such receptor proteins are commonly of low abundance, highly sensitive detection methods are required to study these ligand/receptor interactions. We present a protocol for an inexpensive luminescence-based detection setup in which the peptide ligand of interest is extended with the 11-amino acid HiBiT tag. This tag can be quantified easily down to fmol amounts by its ability to reconstitute the enzymatic activity of LgBiT, a truncated version of the Oplophorus gracilirostris luciferase.
分子相互作用的定量和定性生化描述是研究配体/受体对及其结构/功能关系的基础。生物活性肽通常在(亚)纳摩尔浓度下具有活性,这表明它们对其作用部位(特别是受体上的结合部位)具有高亲和力。由于此类受体蛋白通常丰度较低,因此需要高度敏感的检测方法来研究这些配体/受体相互作用。我们提出了一种基于廉价的基于发光的检测设置的方案,其中感兴趣的肽配体通过 11 个氨基酸的 HiBiT 标签进行扩展。通过其重新组成 LgBiT 的酶活性的能力,很容易将该标签定量至飞摩尔数量级,LgBiT 是 Oplophorus gracilirostris 荧光素的截断版本。