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Targeted Analyte Detection by Standard Addition Improves Detection Limits in MALDI Mass Spectrometry

机译:标准添加的靶向分析物检测可提高MALDI质谱中的检测限

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摘要

Matrix-assisted laser desorption/ionization has proven an effective tool for fast and accurate determination of many molecules. However, the detector sensitivity and chemical noise compromise the detection of many invaluable low-abundance molecules from biological and clinical samples. To challenge this limitation, we developed a targeted analyte detection (TAD) technique. In TAD, the target analyte is selectively elevated by spiking a known amount of that analyte into the sample, thereby raising its concentration above the noise level, where we take advantage of the improved sensitivity to detect the presence of the endogenous analyte in the sample. We assessed TAD on three peptides in simple and complex background solutions with various exogenous analyte concentrations in two MALDI matrices. TAD successfully improved the limit of detection (LOD) of target analytes when the target peptides were added to the sample in a concentration close to optimum concentration. The optimum exogenous concentration was estimated through a quantitative method to be approximately equal to the original LOD for each target. Also, we showed that TAD could achieve LOD improvements on an average of 3-fold in a simple and 2-fold in a complex sample. TAD provides a straightforward assay to improve the LOD of generic target analytes without the need for costly hardware modifications.
机译:事实证明,基质辅助激光解吸/电离是一种快速,准确测定许多分子的有效工具。但是,检测器的灵敏度和化学噪声会损害从生物学和临床样品中检测到许多宝贵的低丰度分子的能力。为了挑战这一限制,我们开发了目标分析物检测(TAD)技术。在TAD中,通过向样品中掺入已知量的分析物来选择性地提高目标分析物的浓度,从而将其浓度提高到噪声水平以上,在此我们利用提高的灵敏度来检测样品中内源性分析物的存在。我们在两种复杂的MALDI基质中,以各种外源分析物浓度评估了简单和复杂背景溶液中三种肽的TAD。当将目标肽以接近最佳浓度的浓度添加到样品中时,TAD成功改善了目标分析物的检测限(LOD)。通过定量方法估计最佳外源浓度约为每个靶标的原始LOD。同样,我们表明,TAD可以将简单样本的LOD平均提高3倍,将复杂样本的LOD提高2倍。 TAD提供了一种直接的检测方法,可提高通用目标分析物的检测限,而无需进行昂贵的硬件修改。

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