适体
寡核苷酸
微流控
纳米技术
计算生物学
计算机科学
蛋白质检测
化学
工程类
特异性抗体
作者
Yang Bu,Yuze Liu,Anni Hu,Yung Ching Lee,Levent Yobas
摘要
selection process that screens large random nucleic-acid libraries for target-binding sequences-remains labor-intensive, time-consuming, and resource-demanding, often requiring specialized expertise while exhibiting poor efficiency and low success rates. Here, we present Auto-SELEX, a fully automated microfluidic platform that enables rapid discovery of ssDNA aptamers against protein targets, completing each selection round in approximately 30 min, as opposed to days or weeks typically required by conventional or competing approaches. Auto-SELEX integrates continuous-flow free-solution electrokinetic partitioning of target-bound aptamers across an artificial sieve without immobilization or iterative washing, together with plasmonic bead-based PCR using gold nanorods for rapid amplification and library regeneration with integrated purification and thermal elution. The platform enables rapid, automated, and effective aptamer discovery, substantially accelerating the SELEX workflow as demonstrated using two structurally and biochemically distinct protein targets, human immunoglobulin E (IgE, ∼190 kDa) and vitronectin (∼75 kDa), yielding high-affinity and target-specific DNA aptamers after only two to three selection rounds, with dissociation constants below 20 nM and 100 nM, respectively.
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