Pabst Martin, Fagerer Stephan R, Köhling Rudolf, Küster Simon K, Steinhoff Robert, Badertscher Martin, Wahl Fabian, Dittrich Petra S, Jefimovs Konstantins, Zenobi Renato
Department of Chemistry and Applied Biosciences, ETH Zürich , Wolfgang-Pauli-Strasse 10, 8093 Zürich, Switzerland.
Anal Chem. 2013 Oct 15;85(20):9771-6. doi: 10.1021/ac4021775. Epub 2013 Sep 23.
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a fast analysis tool employed for the detection of a broad range of analytes. However, MALDI-MS has a reputation of not being suitable for quantitative analysis. Inhomogeneous analyte/matrix co-crystallization, spot-to-spot inhomogeneity, as well as a typically low number of replicates are the main contributing factors. Here, we present a novel MALDI sample target for quantitative MALDI-MS applications, which addresses the limitations mentioned above. The platform is based on the recently developed microarray for mass spectrometry (MAMS) technology and contains parallel lanes of hydrophilic reservoirs. Samples are not pipetted manually but deposited by dragging one or several sample droplets with a metal sliding device along these lanes. Sample is rapidly and automatically aliquoted into the sample spots due to the interplay of hydrophilic/hydrophobic interactions. With a few microliters of sample, it is possible to aliquot up to 40 replicates within seconds, each aliquot containing just 10 nL. The analyte droplet dries immediately and homogeneously, and consumption of the whole spot during MALDI-MS analysis is typically accomplished within few seconds. We evaluated these sample targets with respect to their suitability for use with different samples and matrices. Furthermore, we tested their application for generating calibration curves of standard peptides with α-cyano-4-hdydroxycinnamic acid as a matrix. For angiotensin II and [Glu(1)]-fibrinopeptide B we achieved coefficients of determination (r(2)) greater than 0.99 without the use of internal standards.
基质辅助激光解吸/电离质谱(MALDI-MS)是一种用于检测多种分析物的快速分析工具。然而,MALDI-MS素有不适合定量分析的名声。分析物/基质共结晶不均匀、斑点间不均匀以及通常重复次数较少是主要影响因素。在此,我们展示了一种用于定量MALDI-MS应用的新型MALDI样品靶标,它解决了上述局限性。该平台基于最近开发的质谱微阵列(MAMS)技术,包含平行排列的亲水性储液器。样品不是手动移液,而是通过用金属滑动装置沿着这些通道拖动一个或几个样品液滴来沉积。由于亲水/疏水相互作用,样品迅速自动分装到样品斑点中。用几微升样品,几秒钟内就可以分装多达40个重复样品,每个分装样品仅含10 nL。分析物液滴立即均匀干燥,在MALDI-MS分析过程中整个斑点的消耗通常在几秒钟内完成。我们评估了这些样品靶标对于不同样品和基质的适用性。此外,我们测试了它们用于以α-氰基-4-羟基肉桂酸作为基质生成标准肽校准曲线的应用。对于血管紧张素II和[Glu(1)]-纤维蛋白肽B,我们在不使用内标的情况下获得了大于0.99的决定系数(r²)。