Department of Pharmacy, University of Copenhagen, Universitetsparken 2, 2100, Copenhagen, Denmark.
Global Research Technologies, Novo Nordisk AS, 2760, Måløv, Denmark.
Anal Bioanal Chem. 2020 Jun;412(15):3559-3571. doi: 10.1007/s00216-020-02609-5. Epub 2020 Apr 6.
One of the most attractive aspects of microfluidic chips is their capability of integrating several functional units into one single platform. In particular, enzymatic digestion and chemical separation are important steps in processing samples for many biochemical assays. This study presents the development and application of a free-flow electrophoresis microfluidic chip, and its upstream combination with an enzyme microreactor with immobilized pepsin in the same miniaturized platform. The whole microfluidic chip was fabricated by making use of thiol-ene click chemistry. As a proof of concept, different fluorescent dyes and labeled amino acids were continuously separated in the 2D electrophoretic channel. The protease pepsin was immobilized using a covalent linkage with ascorbic acid onto a high-surface monolithic support, also made of thiol-ene. To show the potential of the microfluidic chip for continuous sample preparation and analysis, an oligopeptide was enzymatically digested, and the resulting fragments were separated and collected in a single step (prior to mass spectrometric detection), without the need of further time-consuming liquid handling steps.
微流控芯片最吸引人的特点之一是能够将多个功能单元集成到一个单一平台上。特别是,酶消化和化学分离是许多生化分析中处理样品的重要步骤。本研究提出了一种自由流电泳微流控芯片的开发和应用,以及其在同一小型化平台上与固定化胃蛋白酶的酶微反应器的上游组合。整个微流控芯片是利用硫醇-烯点击化学反应制造的。作为概念验证,不同的荧光染料和标记氨基酸在 2D 电泳通道中连续分离。蛋白酶胃蛋白酶通过与抗坏血酸的共价键固定在由硫醇-烯制成的高表面积整体式支撑物上。为了展示微流控芯片在连续样品制备和分析方面的潜力,对寡肽进行了酶解,所得片段在单个步骤中进行分离和收集(在进行质谱检测之前),无需进一步耗时的液体处理步骤。