Ho Felix M, Hall Elizabeth A H
Institute of Biotechnology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QT, UK.
Biosens Bioelectron. 2004 Nov 15;20(5):1001-10. doi: 10.1016/j.bios.2004.06.017.
A new displacement hybridisation method is reported using a single strand DNA probe, labelled with an acceptor fluorophore (oregon green 488). Detection of double stranded sample target is shown, with discrimination between the probe, duplexed during the assay, and free single stranded probe DNA achieved through the FRET from a donor grove fluorophore (Hoechst 33258). A model for the kinetics of the displacement assay is presented and the course of the assay predicted according to probe/target ratios and sequence. The modelled predictions are consistent with the experimental data showing single base pair mismatch discrimination. The pattern of response according to the mismatch/perfect complement ratio in a mixed sample is also considered with an allele-discrimination ratio lying between the homozygous gene and total mismatch case, according to ratio. The assay is shown to be tolerant of different probe concentrations and ratios and through the dual wavelength recorded signals from donor and FRET acceptor, internal baseline correction is achieved with excellent noise reduction through ratiometric measurement.
报道了一种新的置换杂交方法,该方法使用用受体荧光团(俄勒冈绿488)标记的单链DNA探针。展示了对双链样品靶标的检测,通过供体沟荧光团(Hoechst 33258)的荧光共振能量转移(FRET)实现了对在检测过程中双链化的探针与游离单链探针DNA的区分。提出了置换检测动力学模型,并根据探针/靶标比例和序列预测了检测过程。模型预测与显示单碱基对错配区分的实验数据一致。还考虑了混合样品中根据错配/完全互补比例的响应模式,根据比例,等位基因区分比例介于纯合基因和完全错配情况之间。该检测方法显示出对不同探针浓度和比例的耐受性,并且通过记录供体和FRET受体的双波长信号,通过比率测量实现了内部基线校正,具有出色的降噪效果。