Liu Zheng-Chun, Zhang Xin, He Nong-Yue, Lu Zu-Hong, Chen Zhen-Cheng
Institute of Biomedical Engineering, School of Info-Physics and Geomatics Engineering, Central South University, Changsha, 410083, China.
Colloids Surf B Biointerfaces. 2009 Jul 1;71(2):238-42. doi: 10.1016/j.colsurfb.2009.02.013. Epub 2009 Feb 24.
We demonstrated the use of X-ray photoelectron spectroscopy (XPS) to study DNA hybridization. Target DNA labeled with hexachloro-fluorescein (HEX) was hybridized to DNA arrays with four different probes. Each probe dot of the hybridized arrays was detected with XPS. The XPS Cl2p peak areas were found to decrease with an increase in mismatched bases in DNA probes. The Cl2p core-level peak area ratio of a probe perfectly matched to one, two and three base-mismatched probes accorded well with the results of conventional fluorescent imaging, which shows that XPS is a potential tool for analyzing DNA arrays. The DNA arrays' hybridization efficiency was assessed by the molar ratio of chlorine to phosphorus in a DNA strand, which was determined from the relevant XPS Cl2p and P2p core-level peak areas after hybridization. This could provide a new method to detect DNA hybridization efficiency.
我们展示了使用X射线光电子能谱(XPS)来研究DNA杂交。用六氯荧光素(HEX)标记的靶DNA与带有四种不同探针的DNA阵列杂交。用XPS检测杂交阵列的每个探针点。发现XPS Cl2p峰面积随着DNA探针中错配碱基数量的增加而减小。与一个、两个和三个碱基错配探针完全匹配的探针的Cl2p核心能级峰面积比与传统荧光成像结果吻合良好,这表明XPS是分析DNA阵列的一种潜在工具。通过DNA链中氯与磷的摩尔比评估DNA阵列的杂交效率,该摩尔比是在杂交后根据相关的XPS Cl2p和P2p核心能级峰面积确定的。这可以提供一种检测DNA杂交效率的新方法。