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使用表面增强激光解吸电离飞行时间质谱法检测和分析蓝藻肽肝毒素微囊藻毒素和节球藻毒素。

Detection and analysis of the cyanobacterial peptide hepatotoxins microcystin and nodularin using SELDI-TOF mass spectrometry.

作者信息

Yuan Moucun, Carmichael Wayne W

机构信息

Department of Biological Sciences, Wright State University, 025A Fawcett Hall, 3640 Colonel Glen Highway, Dayton, OH 45435-0001, USA.

出版信息

Toxicon. 2004 Oct;44(5):561-70. doi: 10.1016/j.toxicon.2004.07.015.

Abstract

Surface-enhanced laser desorption ionization mass spectrometry (SELDI-TOFMS) was used to develop a new and useful method for determination and identification of the cyanobacterial (blue-green algae) toxins: microcystin and nodularin. The technique, combining chromatography and MS, enables microcystin/nodularin capture, purification, analysis, and processing from complex biological mixtures directly onto a hydrophobic chip. Factors affecting ion intensities, including matrix concentration and laser intensity, were investigated to optimize sensitivity of the method. Microcystins and nodularin were analyzed for femtomolar sensitivity (about 2.5 pg microcystin-LR in 2 microl water). Samples of blood sera and liver tissue were spiked with microcystin-LR and analyzed. The detection limit was 1 ng in 2 microl blood sera solution. Reactions of microcystins by compounds containing mercaptan groups, such as dithiothreitol, aminoethanethiol and protein phosphatase 1, were examined on the chip by mass spectrometry. Formation of the microcystin-dithiothreitol conjugate was used to confirm the target compounds. The MS/MS data obtained showed the presence of the microcystin conjugate. The reaction position of the toxin with target compound was confirmed by a series of MS/MS fragment ions. The protein profile of microcystins reacting with protein phosphatase 1 was also obtained from the SELDI-TOF mass spectra.

摘要

表面增强激光解吸电离质谱法(SELDI-TOFMS)被用于开发一种测定和鉴定蓝藻(蓝绿藻)毒素:微囊藻毒素和节球藻毒素的新的实用方法。该技术结合了色谱法和质谱法,能够直接从复杂的生物混合物中捕获、纯化、分析和处理微囊藻毒素/节球藻毒素到疏水芯片上。研究了影响离子强度的因素,包括基质浓度和激光强度,以优化该方法的灵敏度。分析了微囊藻毒素和节球藻毒素的飞摩尔灵敏度(2微升水中约2.5皮克微囊藻毒素-LR)。向血清和肝组织样本中添加微囊藻毒素-LR并进行分析。检测限为2微升血清溶液中1纳克。通过质谱法在芯片上检测了微囊藻毒素与含巯基化合物(如二硫苏糖醇、氨基乙硫醇和蛋白磷酸酶1)的反应。微囊藻毒素-二硫苏糖醇共轭物的形成用于确认目标化合物。获得的MS/MS数据显示了微囊藻毒素共轭物的存在。通过一系列MS/MS碎片离子确认了毒素与目标化合物的反应位置。还从SELDI-TOF质谱图中获得了微囊藻毒素与蛋白磷酸酶1反应的蛋白质谱。

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