DNA
化学
分析物
碱基对
双绞线
荧光
基因组DNA
计算生物学
DNA测序
生物物理学
分子生物学
核苷酸
生物化学
基因
生物
物理
物理化学
量子力学
作者
Yuting Gao,Zhenyan He,Xuewen He,Haoke Zhang,Jun Weng,Xiangliang Yang,Fanling Meng,Liang Luo,Ben Zhong Tang
摘要
Simple, rapid, and sensitive assays of DNA sequence hold great importance in genetic analysis, clinical diagnosis, and molecular biology research. Most current methods for DNA detection, based on the complementary base pairing, require hybridization with intricately modified single-stranded DNA (ssDNA) probes or analytes. Herein, we have developed a powerful molecule with aggregation-induced emission (AIE) characteristic, namely, TPBT, which can specifically recognize double-stranded DNA (dsDNA) by emitting out a unique dual-color fluorescent signal of red (∼640 nm) and green (∼537 nm). The red-color emission at around 640 nm is observed when TPBT binds with dsDNA, ssDNA, proteins, and other polyanionic analytes. However, the green emission at around 537 nm is demonstrated to be the exclusive response of TPBT to dsDNA, which is closely related to the conformational change of TPBT upon groove binding. More strikingly, TPBT can distinguish single-nucleotide polymorphisms (SNPs) in a dsDNA sequence and detect the DNA damage suffered from UV light with ultrahigh sensitivity and specificity. This label-free, AIEgen-based dsDNA assay method is facile, robust, and universal, which will lead to major advances in genomic and disease diagnosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI