化学
适体
数字聚合酶链反应
选择(遗传算法)
计算生物学
纳米技术
聚合酶链反应
分子生物学
生物化学
人工智能
基因
计算机科学
生物
材料科学
作者
Zerui Wu,Wei Yao,Jinyu Chen,Yonghao Chen,Zida Li,Weiping Ding,Liqun He,Peng Hu
出处
期刊:Talanta
[Elsevier BV]
日期:2025-03-11
卷期号:292: 127924-127924
被引量:3
标识
DOI:10.1016/j.talanta.2025.127924
摘要
Aptamers are potent alternatives to antibodies in applications including diagnostics and disease treatment. These synthetic molecules are generated from sequences identified through specific targets within an aptamer pool of random sequences, approximately 10^15 in size, via the Systematic Evolution of Ligands by Exponential Enrichment (SELEX) process. Nevertheless, SELEX encompasses repetitive, time/money-consuming and stochastic methodologies. In this study, we introduce a method for the direct acquisition of target aptamers in a single step, rapidly identifying the aptamers of interest. Single molecules of aptamers are first encapsulated into droplets and amplified therein, and the fluorescence in the droplets will be active upon binding between the aptamers with the target with good affinity. Subsequent identification and sorting of these fluorescing droplets enable the immediate acquisition of desired aptamers without the need for synthesizing them based on selected sequences. This digital selection process bypasses traditional sequencing, thereby reducing stochastic events and costs associated with repeated sequencing, as well as mitigating the uncertainties tied to the synthesis of aptamers. Our proof-of-concept findings suggest that this straightforward yet effective strategy can directly yield aptamers, thereby enhancing the exploration of aptamer biology and promoting the development of aptamer-based applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI