Jiang Xiafei, Liu Haisheng, Khusbu Farjana Yeasmin, Ma Changbei, Ping Anqi, Zhang Qiling, Wu Kefeng, Chen Mingjian
School of Life Sciences, Central South University, Changsha, 410013, China.
School of Life Sciences, Central South University, Changsha, 410013, China.
Anal Biochem. 2018 Aug 15;555:55-58. doi: 10.1016/j.ab.2018.06.014. Epub 2018 Jun 17.
In this paper, we have developed a label-free and rapid fluorescence assay for the detection of exonuclease III (exo III) activity via thioflavin T (ThT) as the G-quadruplex inducer. In this assay, a hairpin probe (HP) with a 5'-guanine-rich (G-rich) sequence is employed as the substrate for exo III. In the presence of exo III, HP can be digested at 3'-OH termini releasing 5'-G-rich sequence. Then, the 5'-G-rich sequence folds into a G-quadruplex, which can be recognized quickly by the ThT dye resulting in an increase in fluorescence emission. This strategy can detect exo III activity as low as 0.5 U/mL. This assay is simple and of low cost without the requirement of labeling with a fluorophore-quencher pair.
在本文中,我们开发了一种无标记的快速荧光检测方法,用于通过硫黄素T(ThT)作为G-四链体诱导剂来检测核酸外切酶III(exo III)的活性。在该检测方法中,具有5'-富含鸟嘌呤(富含G)序列的发夹探针(HP)被用作exo III的底物。在exo III存在的情况下,HP可在3'-OH末端被消化,释放出5'-富含G的序列。然后,5'-富含G的序列折叠成G-四链体,可被ThT染料快速识别,导致荧光发射增加。该策略可检测低至0.5 U/mL的exo III活性。该检测方法简单且成本低,无需用荧光团-猝灭剂对进行标记。