Anal Chem. 2019 Aug 6;91(15):9925-9931. doi: 10.1021/acs.analchem.9b01596. Epub 2019 Jul 24.
Here we present a new analytical method where immunoconcentration of the analyte is coupled to quantitative matrix-assisted laser desorption ionization time of flight mass spectrometry (MALDI-TOF MS) analysis allowing in minutes the identification and highly sensitive quantitation of microcystins (MCs) as model targets. The key element is a site-specific biotinylated nanobody of broad cross-reactivity with microcystins. The single biotin moiety at the C-terminus and the small size of the nanobody (15 kDa) enable its oriented and tightly packed immobilization on magnetic beads, providing a highly efficient capture of the toxin. The binding capacity of the bioadsorbent is partially loaded with an easily synthesized internal standard for MS quantitation. After capture, the beads are directly dispensed on the MALDI-TOF MS target enabling the identification and sensitive quantitation of the microcystin (MC) congeners. Since salts and contaminants are removed during the concentration step, no cleanup or other sample treatments are needed. The method was validated with a large number of water and serum samples with excellent precision and recovery at quantitation limits of 0.025 μg/L of MC.
在这里,我们提出了一种新的分析方法,将分析物的免疫浓缩与定量基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)分析相结合,可在数分钟内鉴定和高度灵敏地定量微囊藻毒素(MCs)作为模型靶标。关键要素是一种具有广泛交叉反应性的针对微囊藻毒素的特异性生物素化纳米抗体。C 末端的单个生物素部分和纳米抗体的小尺寸(15 kDa)使其能够在磁性珠上定向且紧密地固定,从而高效捕获毒素。生物吸附剂的结合能力部分用易于合成的 MS 定量内部标准进行负载。捕获后,将珠直接分配到 MALDI-TOF MS 靶标上,从而能够鉴定和灵敏定量微囊藻毒素(MC)同系物。由于在浓缩步骤中去除了盐和污染物,因此不需要进行清洗或其他样品处理。该方法经过大量水和血清样品的验证,在定量限为 0.025 μg/L MC 时具有出色的精密度和回收率。