Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Flemingovo nám. 2, 116 10, Prague 6, Czech Republic.
Department of Biochemistry, Faculty of Science, Charles University, 12840, Prague 2, Czech Republic.
Anal Bioanal Chem. 2021 Jul;413(17):4531-4543. doi: 10.1007/s00216-021-03423-3. Epub 2021 May 29.
We adapted a radioligand receptor binding assay for measuring insulin levels in unknown samples. The assay enables rapid and accurate determination of insulin concentrations in experimental samples, such as from insulin-secreting cells. The principle of the method is based on the binding competition of insulin in a measured sample with a radiolabeled insulin for insulin receptor (IR) in IM-9 cells. Both key components, radiolabeled insulin and IM-9 cells, are commercially available. The IR binding assay was used to determine unknown amounts of insulin secreted by MIN6 β cell line after stimulation with glucose, arginine, ornithine, dopamine, and serotonin. The experimental data obtained by the IR binding assay were compared to the results determined by RIA kits and both methods showed a very good agreement of results. We observed the stimulation of glucose-induced insulin secretion from MIN6 cells by arginine, weaker stimulation by ornithine, but inhibitory effects of dopamine. Serotonin effects were either stimulatory or inhibitory, depending on the concentration of serotonin used. The results will require further investigation. The study also clearly revealed advantages of the IR binding assay that allows the measuring of a higher throughput of measured samples, with a broader range of concentrations than in the case of RIA kits. The IR binding assay can provide an alternative to standard RIA and ELISA assays for the determination of insulin levels in experimental samples and can be especially useful in scientific laboratories studying insulin production and secretion by β cells and searching for new modulators of insulin secretion.
我们改编了一种放射性配体受体结合测定法,用于测量未知样本中的胰岛素水平。该测定法可快速准确地确定实验样本中的胰岛素浓度,例如来自胰岛素分泌细胞的样本。该方法的原理基于在测量样本中胰岛素与放射性标记胰岛素对 IM-9 细胞中胰岛素受体(IR)的结合竞争。两种关键成分,放射性标记胰岛素和 IM-9 细胞,均可商购获得。IR 结合测定法用于测定葡萄糖、精氨酸、鸟氨酸、多巴胺和 5-羟色胺刺激后的 MIN6 细胞系分泌的未知量的胰岛素。通过 IR 结合测定法获得的实验数据与 RIA 试剂盒确定的结果进行了比较,两种方法的结果均非常吻合。我们观察到精氨酸刺激 MIN6 细胞葡萄糖诱导的胰岛素分泌,鸟氨酸的刺激作用较弱,但多巴胺具有抑制作用。5-羟色胺的作用取决于所使用的 5-羟色胺浓度,可能是刺激作用也可能是抑制作用。结果需要进一步研究。该研究还清楚地显示了 IR 结合测定法的优势,它允许测量更多的测量样本,并且浓度范围比 RIA 试剂盒更宽。IR 结合测定法可替代标准 RIA 和 ELISA 测定法,用于测定实验样本中的胰岛素水平,对于研究β细胞胰岛素产生和分泌以及寻找新的胰岛素分泌调节剂的科学实验室特别有用。