Department of Life Science , Hanyang University , Seoul 04763 , Republic of Korea.
Research Institute for Natural Sciences and Research Institute for Convergence of Basic Sciences , Hanyang University , Seoul 04763 , Republic of Korea.
Anal Chem. 2019 Aug 6;91(15):10064-10072. doi: 10.1021/acs.analchem.9b01991. Epub 2019 Jul 22.
Although low-molecular-weight (LMW) biothiols function as a disease indicator in plasma, rapidly and effectively analyzing them remains challenging in the extracellular oxidative environment due to technical difficulties. Here, we report a newly designed, affinity pulldown platform using a -derived organic hydroperoxide resistance regulatory (OhrR) protein and its operator dsDNA for rapid and cost-effective analyses of plasma LMW biothiols. In the presence of organic hydroperoxide, LMW biothiols triggered the rapid dissociation of FAM-labeled dsDNA from FLAG-tagged OhrR via S-thiolation of OhrR on anti-FLAG antibody-coated beads, which led to a strong increase of fluorescence intensity in the supernatant after pulldown. This method was easily extended by using a reducing agent to detect free and total LMW biothiols simultaneously in mouse plasma. Unlike free plasma LMW biothiols, total plasma LMW biothiols were more elevated in ΔLDLR mice than those in normal mice. Owing to the rapid dissociation of OhrR/dsDNA complexes in response to LMW biothiols, this pulldown platform is immediately suitable for monitoring rapid redox changes in plasma LMW biothiols as well as studying oxidative stress and diseases in blood.
尽管低分子量(LMW)生物硫醇在血浆中作为疾病指标发挥作用,但由于技术困难,在细胞外氧化环境中快速有效地分析它们仍然具有挑战性。在这里,我们报告了一种新设计的亲和下拉平台,该平台使用衍生的有机过氧化物抗性调节(OhrR)蛋白及其操纵子 dsDNA 进行快速且具有成本效益的血浆 LMW 生物硫醇分析。在有机过氧化物存在下,LMW 生物硫醇通过 S-硫醇化作用触发 FAM 标记的 dsDNA 与抗 FLAG 抗体包被珠上的 FLAG 标记的 OhrR 快速解离,这导致下拉后上清液中的荧光强度强烈增加。通过使用还原剂,该方法很容易扩展,以同时检测小鼠血浆中的游离和总 LMW 生物硫醇。与游离血浆 LMW 生物硫醇不同,与正常小鼠相比,Δ LDLR 小鼠中的总血浆 LMW 生物硫醇水平更高。由于 OhrR/dsDNA 复合物对 LMW 生物硫醇的快速解离,该下拉平台立即适用于监测血浆 LMW 生物硫醇中的快速氧化还原变化,以及研究血液中的氧化应激和疾病。