基因分型
多路复用
SNP基因分型
SNP公司
生物
单核苷酸多态性
分子反转探针
聚合酶链反应
遗传学
计算生物学
多重聚合酶链反应
寡核苷酸
分子生物学
DNA
基因型
基因
作者
Woongsun Choi,Eunhye Park,Seojin Bae,Kyung‐Hak Choi,Sangeun Han,Kuk‐Hui Son,Do Young Lee,Il‐Joo Cho,Hyejeong Seong,Kyo Seon Hwang,Jwa‐Min Nam,Jungkyu Choi,Hyojin Lee,Nakwon Choi
出处
期刊:Small
[Wiley]
日期:2021-12-19
卷期号:18 (8)
被引量:11
标识
DOI:10.1002/smll.202105538
摘要
Single nucleotide polymorphisms (SNPs) that can alter phenotypes of individuals play a pivotal role in disease development and, more importantly, responses to therapy. However, SNP genotyping has been challenging due to the similarity of SNP alleles and their low concentration in biological samples. Sequence-specific nanoparticle with interpretative toehold-mediated sequence decoding in hydrogel (SWITCH) for multiplex SNP genotyping is presented. The encoding with gold nanoparticle probes transduces each SNP target to ≈1000 invaders with prominently different sequences between wild and mutant types, featuring polymerase chain reaction (PCR)-free amplification. Subsequently, the toehold-mediated DNA replacement in hydrogel microparticles decodes the invaders via SNP-specific fluorescence signals. The 4-plex detection of the warfarin-associated SNP targets spiked in commercially validated human serum (S1-100ML, Merck) is successfully demonstrated with excellent specificity. This work is the first technology development presenting PCR-free, multiplex SNP genotyping with a single reporting fluorophore, to the best of knowledge.
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