Goodrich Terry T, Lee Hye Jin, Corn Robert M
Department of Chemistry, University of Wisconsin, Madison, Wisconsin, USA.
J Am Chem Soc. 2004 Apr 7;126(13):4086-7. doi: 10.1021/ja039823p.
A novel surface enzymatic reaction scheme that amplifies the optical response of RNA microarrays to the binding of complementary DNA is developed for the direct detection and analysis of genomic DNA. The enzyme RNase H is shown to selectively and repeatedly destroy RNA from DNA-RNA heteroduplexes on gold surfaces; when used in conjunction with the label-free technique of surface plasmon resonance (SPR) imaging, DNA oligonucleotides can be detected at a concentration of 1 fM. This enzymatically amplified SPR imaging methodology is then utilized to detect and identify the presence of the TSPY gene in human genomic DNA without PCR amplification.
一种新型表面酶促反应方案被开发出来,用于基因组DNA的直接检测和分析,该方案可放大RNA微阵列对互补DNA结合的光学响应。结果表明,核糖核酸酶H(RNase H)能选择性且反复地破坏金表面DNA-RNA杂交双链中的RNA;当与表面等离子体共振(SPR)成像的无标记技术结合使用时,DNA寡核苷酸的检测浓度可达1 fM。然后,利用这种酶促放大的SPR成像方法,无需PCR扩增即可检测和鉴定人类基因组DNA中TSPY基因的存在。