Identification of Butyrylcholinesterase-Derived Small Molecule Peptides Indicative of Novichok Nerve Agent Exposures.

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL Chemical Research in Toxicology Pub Date : 2025-01-14 DOI:10.1021/acs.chemrestox.4c00397
Susan O Kim, Tonya T Lansing, Jonas W Perez, Brooke G Pantazides, Brian S Crow, Thomas A Blake
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Abstract

Novichok nerve agents, such as A-230, A-232, and A-234, were classified as Schedule 1 chemicals under the Chemical Weapons Convention (CWC) by the Organisation for the Prohibition of Chemical Weapons (OPCW) following poisoning incidents in 2018. As a result, the production, storage, and use of these chemicals are strictly prohibited by CWC signatory nations. The identification of biomarkers indicating Novichok exposure in humans is crucial for prompt detection and response to potential incidents involving these banned chemical weapons. In this study, BChE was isolated from human serum samples exposed to Novichok nerve agents in vitro using immunomagnetic capture, followed by enzymatic digestion with Pronase or proteinase K to generate new peptide biomarkers indicative of exposure. We identified nine previously unpublished Novichok-adducted peptides generated through enzymatic digestion with proteinase K and Pronase using liquid chromatography-high-resolution mass spectrometry. Two peptides, [Agent]-serine-alanine for proteinase K digestion and [Agent]-serine-alanine-glycine for Pronase digestion, were selected for optimization due to their abundance. The analysis was subsequently transferred to an LC-triple quadrupole system to enhance throughput and detect these new biomarkers at the limits of detection corresponding to BChE inhibition levels of 3.90% or less. These additional biomarkers can improve laboratory preparedness for OPCW-designated biomedical testing laboratories as well as other clinical and investigative laboratories tasked with responding to emergencies involving these highly toxic chemicals.

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表明诺维乔克神经毒剂暴露的丁基胆碱酯酶衍生小分子肽的鉴定。
在2018年发生中毒事件后,诺维乔克神经毒剂,如A-230、A-232和A-234,被禁止化学武器组织(禁化武组织)列为《化学武器公约》(CWC)附表1化学品。因此,这些化学品的生产、储存和使用受到《禁止化学武器公约》签署国的严格禁止。识别表明人类暴露于诺维乔克的生物标志物对于迅速发现和应对涉及这些被禁化学武器的潜在事件至关重要。在这项研究中,利用免疫磁捕获技术从暴露于诺维乔克神经毒剂的人血清样本中分离出BChE,然后用Pronase或蛋白酶K进行酶切,产生新的肽生物标志物,表明暴露。我们使用液相色谱-高分辨率质谱法鉴定了9个以前未发表的诺维乔克内合肽,这些肽是通过蛋白酶K和Pronase酶切产生的。因其丰富度,选择用于蛋白酶K消化的[Agent]-丝氨酸-丙氨酸和用于Pronase消化的[Agent]-丝氨酸-丙氨酸-甘氨酸进行优化。随后将分析转移到lc -三重四极杆系统,以提高通量,并在相应的BChE抑制水平为3.90%或更低的检测限下检测这些新的生物标志物。这些额外的生物标记物可以改善禁化武组织指定的生物医学测试实验室以及负责应对涉及这些剧毒化学品的紧急情况的其他临床和调查实验室的实验室准备工作。
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来源期刊
CiteScore
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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