Division of BioAnalytical Chemistry, Amsterdam Institute of Molecules, Medicines and Systems , Vrije Universiteit Amsterdam , Amsterdam 1081 HZ , The Netherlands.
LaserLaB , Vrije Universiteit Amsterdam , Amsterdam 1081 HZ , The Netherlands.
Anal Chem. 2019 Aug 20;91(16):10458-10466. doi: 10.1021/acs.analchem.9b01261. Epub 2019 Aug 2.
High-throughput screening platforms for the identification of bioactive compounds in mixtures have become important tools in the drug discovery process. Miniaturization of such screening systems may overcome problems associated with small sample volumes and enhance throughput and sensitivity. Here we present a new screening platform, coined picofractionation analytics, which encompasses microarray bioassays and mass spectrometry (MS) of components from minute amounts of samples after their nano liquid chromatographic (nanoLC) separation. Herein, nanoLC was coupled to a low-volume liquid dispenser equipped with pressure-fed solenoid valves, enabling 50-nL volumes of column effluent (300 nL/min) to be discretely deposited on a glass slide. The resulting fractions were dried and subsequently bioassayed by sequential printing of nL-volumes of reagents on top of the spots. Unwanted evaporation of bioassay liquids was circumvented by employing mineral oil droplets. A fluorescence microscope was used for assay readout in kinetic mode. Bioassay data were correlated to MS data obtained using the same nanoLC conditions in order to assign bioactives. The platform provides the possibility of freely choosing a wide diversity of bioassay formats, including those requiring long incubation times. The new method was compared to a standard bioassay approach, and its applicability was demonstrated by screening plasmin inhibitors and fibrinolytic bioactives from mixtures of standards and snake venoms, revealing active peptides and coagulopathic proteases.
高通量筛选平台用于鉴定混合物中的生物活性化合物已成为药物发现过程中的重要工具。此类筛选系统的小型化可能克服与小样本量相关的问题,并提高通量和灵敏度。在这里,我们提出了一种新的筛选平台,称为皮升级分分析,它包括微阵列生物测定和质谱 (MS) 分析,用于从小量样品中分离出的成分,这些成分经过纳米液相色谱 (nanoLC) 分离。在此,nanoLC 与低体积液体分配器耦合,该分配器配备有压力进料电磁阀,可将 50-nL 体积的柱洗脱液(300 nL/min)离散地沉积在玻璃载玻片上。所得馏分干燥后,通过在斑点上连续打印 nL 体积的试剂进行顺序生物测定。通过使用矿物油滴来避免生物测定液的不必要蒸发。荧光显微镜用于以动力学模式进行测定读数。为了分配生物活性物质,将生物测定数据与使用相同 nanoLC 条件获得的 MS 数据相关联。该平台提供了自由选择广泛的生物测定格式的可能性,包括需要长时间孵育的格式。新方法与标准生物测定方法进行了比较,并通过从标准和蛇毒液混合物中筛选纤溶抑制剂和纤维蛋白溶解生物活性物质,证明了其适用性,揭示了活性肽和凝血酶蛋白酶。