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基于分子信标的生物分析方法,用于高度灵敏和选择性检测烟酰胺腺嘌呤二核苷酸和丙氨酸氨基转移酶的活性。

Molecular beacon based bioassay for highly sensitive and selective detection of nicotinamide adenine dinucleotide and the activity of alanine aminotransferase.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Key Laboratory for Bio-Nanotechnology and Molecule Engineering of Hunan Province, Changsha 410082, China.

出版信息

Anal Chem. 2011 Apr 1;83(7):2505-10. doi: 10.1021/ac102742k. Epub 2011 Mar 14.

DOI:10.1021/ac102742k
PMID:21401019
Abstract

We have developed a new approach to detect nicotinamide adenine dinucleotide (NAD(+)) with high specificity and sensitivity using molecular beacons (MBs) and employed it in the investigation of NAD(+) related biological processes, such as calorie restriction and alanine aminotransferase (ALT) activation. The E. coli DNA ligase would catalyze the ligation of two short oligonucleotides that complement with an MB only in the presence of NAD(+), resulting in the opening of the MB and the restoration of fluorescent signal. Thanks to the high sensitivity of the MB probe and the fidelity of E. coli DNA ligase toward its substrates, this approach can detect 0.3 nM NAD(+) with high selectivity against other NAD(+) analogs. This novel assay can also provide a convenient and robust way to analyze NAD(+) in biological samples such as cell lysate. As NAD(+) plays an essential role in many biochemical processes, this method can be used to investigate NAD(+) related life processes. For instance, the effect of calorie restriction on the intracellular NAD(+) level in MCF7 cells has been studied using this new assay. Moreover, this approach was also successfully used to analyze the activity of ALT. Therefore, this novel NAD(+) assay holds wide applicability as an analytical tool in biochemical and biomedical research.

摘要

我们开发了一种使用分子信标(MBs)高特异性和高灵敏度检测烟酰胺腺嘌呤二核苷酸(NAD(+))的新方法,并将其用于研究与 NAD(+)相关的生物学过程,如热量限制和丙氨酸氨基转移酶(ALT)激活。在 NAD(+)存在的情况下,大肠杆菌 DNA 连接酶仅会催化两个与 MB 互补的短寡核苷酸的连接,导致 MB 打开并恢复荧光信号。由于 MB 探针的高灵敏度和大肠杆菌 DNA 连接酶对其底物的保真度,该方法可以高选择性地检测 0.3 nM 的 NAD(+),而不会受到其他 NAD(+)类似物的干扰。这种新的测定方法还可以为分析细胞裂解物等生物样本中的 NAD(+)提供一种方便、稳健的方法。由于 NAD(+)在许多生化过程中起着至关重要的作用,因此该方法可用于研究与 NAD(+)相关的生命过程。例如,使用这种新的测定方法研究了热量限制对 MCF7 细胞内 NAD(+)水平的影响。此外,该方法还成功用于分析 ALT 的活性。因此,这种新型 NAD(+)测定方法作为生化和生物医学研究中的分析工具具有广泛的适用性。

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