Jiang Tieshan, Minunni Maria, Wilson P, Zhang Jian, Turner A P F, Mascini Marco
Life Science College, Hunan Normal University, Changsha 410081, Hunan, PR China.
Biosens Bioelectron. 2005 Apr 15;20(10):1939-45. doi: 10.1016/j.bios.2004.08.040.
A DNA-based surface plasmon resonance (SPR) biosensor has been developed for the detection of TP53 mutation using the inexpensive and commercially available instrument, SPREETA SPR-EVM-BT, from Texas Instruments. A direct immobilisation procedure, based on the coupling of thiol-derivatised oligonucleotide probes (Probe-C6-SH) to bare gold sensor surfaces, was optimized using synthetic oligonucleotides. Hybridisation reactions between the immobilised probe and a short sequence (26 mer) complementary, non-complementary and one-point mutation DNA were then investigated. The main analytical parameters of the sensor system were studied in detail including selectivity, sensitivity, reproducibility and analysis time. Finally, the sensor system was successfully applied to polymerase chain reaction (PCR)-amplified real samples, DNA extracted from both normal, wild-type, (Jurkat) and mutated (Molt 4), carrying the mutation at codon 248 of the TP53 cell lines. The results obtained demonstrate that the DNA-based SPR biosensor was able to distinguish sequences present in the various samples that differ only by one base; and hence, it appears to be a strong candidate technique for the detection of gene mutation.
一种基于DNA的表面等离子体共振(SPR)生物传感器已被开发出来,用于使用德州仪器公司生产的价格低廉且可商购的仪器SPREETA SPR-EVM-BT检测TP53突变。基于硫醇衍生化寡核苷酸探针(Probe-C6-SH)与裸金传感器表面的偶联,采用合成寡核苷酸对直接固定化程序进行了优化。然后研究了固定化探针与短序列(26聚体)互补、非互补和单点突变DNA之间的杂交反应。详细研究了传感器系统的主要分析参数,包括选择性、灵敏度、重现性和分析时间。最后,该传感器系统成功应用于聚合酶链反应(PCR)扩增的实际样品,即从正常野生型(Jurkat)和携带TP53基因第248位密码子突变的突变型(Molt 4)细胞系中提取的DNA。获得的结果表明,基于DNA的SPR生物传感器能够区分仅相差一个碱基的各种样品中的序列;因此,它似乎是一种用于检测基因突变的强大候选技术。