Wood Bayden R
Centre for Biospectroscopy, School of Chemistry, Monash University, 3800, Victoria, Australia.
Chem Soc Rev. 2016 Apr 7;45(7):1980-98. doi: 10.1039/c5cs00511f.
Since Watson and Crick's historical papers on the structure and function of DNA based on Rosalind Franklin's and Maurice Wilkin's X-ray diffraction patterns tremendous scientific curiosity has been aroused by the unique and dynamic structure of the molecule of life. A-DNA and B-DNA represent different conformations of the DNA molecule, which is stabilised by hydrogen interactions between base pairs, stacking interactions between neighboring bases and long-range intra- and inter-backbone forces. This review highlights the contribution Fourier transform infrared (FTIR) spectroscopy has made to the understanding of DNA conformation in relation to hydration and its potential role in clinical diagnostics. The review will first begin by elucidating the main forms of DNA conformation found in nature and the general structures of the A, B and Z forms. This is followed by a detailed critique on infrared spectroscopy applied to DNA conformation highlighting pivotal studies on isolated DNA, polynucleotides, nucleoprotein and nucleohistone complexes. A discussion on the potential of diagnosing cancer using FTIR spectroscopy based on the detection of DNA bands in cells and tissues will ensue, highlighting the recent studies investigating the conformation of DNA in hydrated and dehydrated cells. The method of hydration as a way to facilitate DNA conformational band assignment will be discussed and the conformational change to the A-form upon dehydration will be used to explain the reason for the apparent lack of FTIR DNA signals observed in fixed or air-dried cells and tissues. The advantages of investigating B-DNA in the hydrated state, as opposed to A-DNA in the dehydrated state, are exemplified in a series of studies that show: (1) improved quantification of DNA in cells; (2) improved discrimination and reproducibility of FTIR spectra recorded of cells progressing through the cell cycle; (3) insights into the biological significance of A-DNA as evidenced by an interesting study on bacteria, which can survive desiccation and at the same time undergo the B-A-B transition. Finally, the importance of preserving the B-DNA conformation for the diagnosis of cancer is put forward as way to improve the sensitivity of this powerful technique.
自从沃森和克里克基于罗莎琳德·富兰克林和莫里斯·威尔金斯的X射线衍射图谱发表关于DNA结构和功能的具有历史意义的论文以来,生命分子独特而动态的结构引发了巨大的科学好奇心。A-DNA和B-DNA代表DNA分子的不同构象,DNA分子通过碱基对之间的氢键相互作用、相邻碱基之间的堆积相互作用以及长程骨架内和骨架间作用力得以稳定。本综述重点介绍了傅里叶变换红外(FTIR)光谱在理解与水合作用相关的DNA构象及其在临床诊断中的潜在作用方面所做出的贡献。综述首先将阐明自然界中发现的DNA构象的主要形式以及A、B和Z型的一般结构。接下来将对应用于DNA构象的红外光谱进行详细评论,重点介绍关于分离的DNA、多核苷酸、核蛋白和核组蛋白复合物的关键研究。随后将讨论基于检测细胞和组织中的DNA条带利用FTIR光谱诊断癌症的潜力,重点介绍最近研究水合和脱水细胞中DNA构象的研究。将讨论水合方法作为促进DNA构象带归属的一种方式,并利用脱水后向A-型的构象变化来解释在固定或风干的细胞和组织中观察到明显缺乏FTIR DNA信号的原因。与脱水状态下的A-DNA相反,在水合状态下研究B-DNA的优势在一系列研究中得到了体现,这些研究表明:(1)提高了细胞中DNA的定量;(2)提高了记录处于细胞周期不同阶段的细胞的FTIR光谱的辨别力和重现性;(3)对A-DNA生物学意义的深入了解,这一点在一项关于细菌的有趣研究中得到了证明,该细菌能够在干燥环境中存活并同时经历B-A-B转变。最后,提出保持B-DNA构象对于癌症诊断的重要性,以此作为提高这项强大技术灵敏度的一种方法。