Culha Mustafa, Stokes David, Vo-Dinh Tuan
Advanced Biomedical Science and Technology Group, Oak Ridge National Laboratory, TN 37831-6101, USA.
Expert Rev Mol Diagn. 2003 Sep;3(5):669-75. doi: 10.1586/14737159.3.5.669.
A method of detection for cancer genes, such as B-cell lymphoma 2 gene, has been developed using surface-enhanced Raman scattering-active substrates. This method uses Raman active dye-labeled DNA gene probes and metallic nanostructures as surface-enhanced Raman scattering-active platforms. A self-assembled monolayer system composed of mercapto hexane-labeled, single-strand DNA (SH-(CH2)6-ssDNA/ 6-mercapto-1-hexanol) is formed on a silver surface. The Raman-active dye-labeled gene is hybridized with its complementary probe, which is immobilized on the silver surface. The surface-enhanced Raman gene probes in this study can be used to detect DNA targets via hybridization to complementary DNA probes. The probes do not involve the use of radioactive labels and have great potential to provide both sensitivity and selectivity. The utility of this approach is investigated.
一种利用表面增强拉曼散射活性底物检测癌症基因(如B细胞淋巴瘤2基因)的方法已被开发出来。该方法使用拉曼活性染料标记的DNA基因探针和金属纳米结构作为表面增强拉曼散射活性平台。在银表面形成由巯基己烷标记的单链DNA(SH-(CH2)6-ssDNA/6-巯基-1-己醇)组成的自组装单分子层系统。拉曼活性染料标记的基因与其互补探针杂交,该互补探针固定在银表面。本研究中的表面增强拉曼基因探针可通过与互补DNA探针杂交来检测DNA靶标。这些探针不涉及使用放射性标记,并且在提供灵敏度和选择性方面具有巨大潜力。对该方法的实用性进行了研究。