Nanobiotechnology & Bioanalysis Group, Departament d'Enginyeria Quimica, Universitat Rovira i Virgili, Avinguda Països Catalans, 26, 43007 Tarragona, Spain.
Biosens Bioelectron. 2010 Oct 15;26(2):307-13. doi: 10.1016/j.bios.2010.08.043. Epub 2010 Aug 20.
Cystic fibrosis is one of the most common genetically inherited diseases in Northern Europe, consisting of an inherited defect of chloride transport in the epithelium. Of the several mutations related to CF, the ΔF508 mutation occurs in ca. 70% of the cases. In this work the use of a gold nano-particle supported fluorescence molecular beacon was investigated as an optical sensing platform for the detection of the ΔF508 cystic fibrosis associated mutation. Different parameters such as molecular beacon design, Au nano-particle size, molecular beacon-nano-particle conjugation protocol, molecular beacon loading as well as experimental conditions were evaluated. A 31-base long molecular beacon, containing a 15-base recognition sequence specific for the mutant target, was linked via a thiol modified poly thymine linker (10 bases long) to a 13 nm gold nano-particle and was exposed to mutant and wild type targets, and a clear differentiation was achieved at target concentrations as low as 1 nM.
囊性纤维化是北欧最常见的遗传性疾病之一,由上皮细胞中氯离子转运的遗传缺陷引起。在与 CF 相关的几种突变中,约 70%的病例存在 ΔF508 突变。在这项工作中,研究了金纳米粒子支持的荧光分子信标作为检测 ΔF508 囊性纤维化相关突变的光学传感平台的用途。评估了不同的参数,如分子信标设计、Au 纳米粒子尺寸、分子信标-纳米粒子缀合方案、分子信标加载以及实验条件。一个 31 个碱基长的分子信标,包含一个 15 个碱基的识别序列,特异性针对突变靶标,通过一个硫醇修饰的聚胸腺嘧啶链接(10 个碱基长)连接到一个 13nm 的金纳米粒子上,并暴露于突变和野生型靶标,在靶标浓度低至 1 nM 时就可以清楚地区分。