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Microchip HPLC of Peptides and Proteins

机译:肽和蛋白质的Microchip HPLC

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Rapid microchip reversed-phase HPLC of peptides and proteins at pressure gradients of 12 bar/cm (180 psi/cm) has been performed using a microdevice that integrates subnanoliter on-chip injection and separation with a miniaturized fluorescence detector. Proteins and peptides were separated on a C18 side-chain porous polymer monolith defined by contact lithography, and injection was achieved via a pressure-switchable fluoropolymer valve defined using projection lithography. Preliminary separations of peptide standards and protein mixtures were performed in 40-200 s, and switching between samples with no detectible sample carryover has been performed. The injections and separations were reproducible; the relative standard deviation (RSD) for retention time was 0.03%, and peak area RSD was 3.8%. Sample volumes ranging from 220 to 800 pL could be linearly metered by controlling the pressure injection pulse duration with conventional timing and valving. The current prototype system shows the potential for rapid and autonomous HPLC separations with varying modalities and the potential for direct connection to mass spectrometers at nanospray flow rates.
机译:使用集成了纳纳升芯片上进样和分离与微型化荧光检测器的微装置,已进行了压力梯度为12 bar / cm(180 psi / cm)的肽和蛋白质的快速微芯片反相HPLC。在通过接触光刻定义的C18侧链多孔聚合物整料上分离蛋白质和肽,并通过使用投影光刻定义的压力可切换的含氟聚合物阀实现进样。在40-200 s内对肽标准品和蛋白质混合物进行了初步分离,并且在没有可检测到的样品残留的情况下进行了样品之间的切换。进样和分离是可重现的。保留时间的相对标准偏差(RSD)为0.03%,峰面积RSD为3.8%。通过使用常规的定时和阀门控制压力注入脉冲的持续时间,可以线性计量220至800 pL的样品量。当前的原型系统显示出具有各种模式的快速自动HPLC分离的潜力,以及以纳喷雾流速直接连接到质谱仪的潜力。

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