Mariani Stefano, Scarano Simona, Carrai Maura, Barale Roberto, Minunni Maria
Dipartimento di Chimica "Ugo Schiff", Università di Firenze, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, FI, Italy.
Anal Bioanal Chem. 2015 May;407(14):4023-8. doi: 10.1007/s00216-014-8424-1. Epub 2015 Jan 27.
Optical genotyping of C3435T single nucleotide polymorphisms (SNPs) in unamplified human multidrug resistance (MDR1) gene was here performed by a surface plasmon resonance imaging (SPRi) dual-targeting DNA assay, allowing its selective detection down to 0.18 fM of the whole genomic DNA. The result was achieved by the combination of the rational selection of the DNA probe and an optimized sample pretreatment (i.e., ultrasound fragmentation and thermal denaturation). Some assay developments and tunings were reported in a previously published research, but here, for the first time, the biosensor reliability and its analytical performance were directly tested on the unamplified human DNA extracted from lymphocytes. The assay resulted to be able to differentiate among all the possible genotypes of C3435T (homozygote and heterozygote) in the diluted genomic samples using a label-free approach and by bypassing the classical PCR amplification of the target sequences. Moreover, the reusability of the DNA-based chip allowed up to 40 subsequent measuring cycles, opening new horizons in multi-SNP genotyping based on cheap and daily routine clinical monitoring by optical biosensing.
本文通过表面等离子体共振成像(SPRi)双靶向DNA检测法,对未扩增的人类多药耐药(MDR1)基因中的C3435T单核苷酸多态性(SNP)进行光学基因分型,能够在全基因组DNA低至0.18 fM时对其进行选择性检测。这一结果是通过合理选择DNA探针和优化样品预处理(即超声破碎和热变性)实现的。此前发表的一项研究报告了一些检测方法的改进和调整,但在此首次直接在从淋巴细胞中提取的未扩增人类DNA上测试了生物传感器的可靠性及其分析性能。该检测方法能够使用无标记方法并绕过目标序列的经典PCR扩增,在稀释的基因组样品中区分C3435T的所有可能基因型(纯合子和杂合子)。此外,基于DNA的芯片可重复使用,允许进行多达40个后续测量周期,为基于光学生物传感的廉价日常临床监测的多SNP基因分型开辟了新视野。