Department of Chemistry, Shantou University, Shantou, 515063, China.
Analyst. 2012 Feb 7;137(3):722-8. doi: 10.1039/c1an15855d. Epub 2011 Dec 13.
The DNA sequence recognition study of DNA-targeted anticancer drugs is a theoretical basis for improving the selectivity of anticancer drugs. With the high synergy effect of cocoamidopropyl hydroxy sulfobetaine (HSB), a resonance light scattering (RLS) quenching system for DNA sequence recognition studies of actinomycin D (ACTD) was developed in this contribution. By the strategy, DNA sequence selectivity as well as the recognition mechanisms of ACTD was systematically investigated. The results suggested that ACTD had the selectivity to single-stranded DNA (ssDNA) with an equilibrium constant (K(RLS)) of 12.4 mmol mg(-1). Also it had a preference for Guanine and Cytosine bases with a K(RLS) of 6.69 L mmol(-1). The selectivity mechanism between ACTD and DNA was also well discussed with the help of UV-Vis absorption spectroscopy. Compared with other methods, the RLS quenching system has the advantages of reliability and speediness, and it avoids complex modification processes and is a better bionic system for the above research. Results obtained from this work would supply a theoretical basis for improving anticancer activity and designing similar anticancer drugs.
DNA 靶向抗癌药物的 DNA 序列识别研究是提高抗癌药物选择性的理论基础。本文利用椰油酰胺丙基羟磺基甜菜碱(HSB)的高协同效应,构建了一种吖啶黄素(ACTD)DNA 序列识别研究的共振光散射(RLS)猝灭体系。通过该策略,系统地研究了 ACTD 的 DNA 序列选择性和识别机制。结果表明,ACTD 对单链 DNA(ssDNA)具有选择性,平衡常数(K(RLS))为 12.4mmolmg(-1)。它还优先与鸟嘌呤和胞嘧啶碱基结合,K(RLS)为 6.69Lmmol(-1)。借助紫外可见吸收光谱,还很好地讨论了 ACTD 与 DNA 之间的选择性机制。与其他方法相比,RLS 猝灭体系具有可靠性和快速性的优点,避免了复杂的修饰过程,是上述研究的更好仿生体系。这项工作的结果将为提高抗癌活性和设计类似抗癌药物提供理论依据。