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免疫捕获和液相色谱-串联质谱法灵敏检测炭疽芽孢。

Sensitive detection of Bacillus anthracis spores by immunocapture and liquid chromatography-tandem mass spectrometry.

机构信息

Service de Pharmacologie et d'Immunoanalyse, iBiTec-S, CEA, Gif-sur-Yvette Cedex, France.

出版信息

Anal Chem. 2011 Nov 15;83(22):8675-82. doi: 10.1021/ac2020992. Epub 2011 Oct 18.

Abstract

Bacillus anthracis is one of the most dangerous agents of the bioterrorism threat. We present here a sensitive immuno-liquid chromatography-tandem mass spectrometry (immuno-LC-MS/MS) approach to spore detection in complex environmental samples. It is based on the combined specificity and sensitivity of two techniques: immunocapture and targeted mass spectrometry. The immunocapture step, realized directly on the intact spores, is essential for their selective isolation and concentration from complex environmental samples. After parallel trypsin and Glu-C digestions, proteotypic peptides corresponding to small acid-soluble spore protein-B (SASP-B) are specifically monitored in the multiple reaction monitoring (MRM) mass spectrometry mode. Peptide ratio is carefully monitored and provides an additional level of specificity, which is shown to be highly useful for distinguishing closely related samples and avoiding false-positive/negative results. Sensitivity at the level of the infectious dose is demonstrated, with limits of detection of 7 × 10(3) spores/mL of milk or 10 mg of soil. This mass spectrometry approach is thus complementary to polymerase chain reaction (PCR) techniques.

摘要

炭疽杆菌是生物恐怖威胁中最危险的因子之一。我们在此提出了一种敏感的免疫液相色谱-串联质谱(immuno-LC-MS/MS)方法,用于检测复杂环境样本中的孢子。它基于两种技术的组合特异性和敏感性:免疫捕获和靶向质谱。免疫捕获步骤直接在完整的孢子上进行,对于从复杂的环境样本中选择性分离和浓缩孢子至关重要。经过平行胰蛋白酶和 Glu-C 消化后,特异性监测与小酸溶性孢子蛋白-B(SASP-B)相对应的特征肽,在多重反应监测(MRM)质谱模式下进行。仔细监测肽比,并提供额外的特异性水平,这对于区分密切相关的样本和避免假阳性/阴性结果非常有用。该方法的检测灵敏度达到了感染剂量水平,牛奶中检测限为 7×10(3)个孢子/mL,土壤中检测限为 10 mg。因此,该质谱方法与聚合酶链反应(PCR)技术互补。

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