纳米孔
材料科学
纳米技术
微流控
电阻式触摸屏
生物芯片
生物传感器
小型化
纳米尺度
生物反应器
聚合物囊泡
生物分子
纳米-
纳米流体学
纳米结构
微型反应器
流体学
体积流量
执行机构
固定化酶
作者
Indu A. Chandrasoma,Khurshed Akabirov,Oluwadamilola Fateru,Katie Childers,Swarnagowri Vaidyanathan,Sheila de M. Barros,Maximillian Chibuike,Suresh Shivanka,Matthew Verber,Collin McKinney,Uditha Athapattu,Pubudu Premarathne,Farhad Shiri,Malgorzata A. Witek,Junseo Choi,Adam R. Hall,Sunggook Park,Steven A. Soper
标识
DOI:10.1021/acsami.6c08660
摘要
We report a thermoplastic nanofluidic sensor (exonuclease time-of-flight; X-ToF) fabricated via nanoinjection molding that integrates an immobilized nanoscale enzymatic reactor (INER) directly with a dual in-plane nanopore ToF (DNP-ToF) reader, which not only uses the parameters typically used for resistive pulse sensing (RPS)─normalized event amplitude and time width─but the time taken for a single-molecule to travel between two pores in series. This platform enables the label-free monitoring of complex biological reactions at the single-molecule level. A critical hurdle in integrating such bioenzymatic reactions with RPS is reconciling disparate process step requirements, for example salt effects on an enzymatic reaction and high salt needs for RPS. We addressed this through strategic UV/O 3 surface engineering; an optimized 3.5 min dose created effectively charge-neutral nanopores that maximized capture rates while sustaining a robust ensemble electroosmotic flow (5.33 ± 0.33 × 10 –5 cm 2 V –1 s –1 ) and simultaneously preserving enzyme activity. To demonstrate the sensor’s utility, exoribonuclease 1 (Xrn1) was used as a model. X-ToF successfully deduced the dissociation constant of an input Cas9 RNA to Xrn1 (2.4 ± 0.02 μM –1 ) and monitored in real-time ribonucleotide generation from Cas9 with a cleavage rate of 23 nt/s. Ultimately, this platform serves as a highly versatile tool that can be repurposed for DNA, RNA, or protein sequencing simply by changing the identity of the immobilized enzyme.
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