N-乙酰基-S-(4-羟基-2-丁烯-1-基)-L-半胱氨酸反式和顺式异构体的合成和表征及其在人体尿液中的检测尝试

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-09-03 DOI:10.1016/j.jchromb.2024.124294
Fei Yang , Yi-Yi Cao , Jing Xi , Yang Luan , Na Li , Xin Dong , Xin-Yu Zhang
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引用次数: 0

摘要

1,3-丁二烯(BD)是一种致癌空气污染物。N-乙酰基-S-(4-羟基-2-丁烯-1-基)-L-半胱氨酸(MHBMA3 或 4HBeMA)是一种未明确构型的尿液丁二烯代谢物,被认为是最灵敏的丁二烯生物标志物,自 2012 年以来一直用于常规生物监测。然而,有两个问题仍未得到解决:为什么相对于其他尿液 BD 生物标记物,它的浓度异常高;为什么一些作者报告未检测到该生物标记物,而另一些作者却很容易对其进行定量。为了解决这些问题,我们合成了 MHBMA3 的真实反式和顺式异构体(分别命名为 NE 和 NZ)并对其进行了结构表征,开发了一种同位素稀释 LC-MS/MS 方法对其进行定量,并对来自烧烤店员工(47 人)和酒店行政人员(20 人)的 67 份尿液样本进行了检测。烧烤店员工暴露在烧烤油烟中,而烧烤油烟中的 BD 含量相对较高。结果表明,NE 和 NZ 的核磁共振波谱高度相似,且很难用色谱法很好地分离。核磁共振数据显示,之前大多数研究中调查的 MHBMA3 异构体是 NE。我们没有在任何样品中检测到 NE 和 NZ;不过,在大多数样品中都观察到了高度不等的干扰峰。值得注意的是,在文献中使用的色谱条件下,该峰的保留时间与 NE 的保留时间无法区分。因此,该干扰峰极有可能在以往的研究中被误认为是 NE,从而为尿液中 MHBMA3 浓度较高提供了合理解释。尿液中 MHBMA3 存在的矛盾也是由错误鉴定造成的,因为报告不存在 MHBMA3 的研究人员实际上检测到的是 NZ。因此,我们通过正确识别两种 MHBMA3 异构体,澄清了以往研究中对 MHBMA3 的混淆。人体尿液中 NE 和 NZ 的存在值得进一步研究。
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Synthesis and characterization of the trans- and cis-isomers of N-acetyl-S-(4-hydroxy-2-buten-1-yl)-L-cysteine and their attempted detection in human urine

1,3-Butadiene (BD) is a carcinogenic air pollutant. N-acetyl-S-(4-hydroxy-2-buten-1-yl)-L-cysteine (MHBMA3 or 4HBeMA), an urinary BD metabolite with unspecified configuration, is considered the most sensitive BD biomarker and has been used in routine biomonitoring since 2012. However, two issues remain unaddressed: why its concentrations are unusually high relative to other urinary BD biomarkers and why some authors reported no detection of the biomarker whereas other authors readily quantitated it. To address the issues, we synthesized and structurally characterized the authentic trans- and cis-isomers of MHBMA3 (designated NE and NZ, respectively), developed an isotope-dilution LC-MS/MS method for their quantification, and examined 67 urine samples from barbecue restaurant personnel (n = 47) and hotel administrative staff (n = 20). The restaurant personnel were exposed to barbecue fumes, which contain relatively high concentrations of BD. The results showed that NE and NZ had highly similar NMR spectra, and were difficult to be well separated chromatographically. The NMR data showed that the MHBMA3 isomer investigated in most previous studies was NE. We did not detect NE and NZ in any samples; however, an interfering peak with varying heights was observed in most samples. Notably, under the chromatographic conditions used in the literature, the peak exhibited indistinguishable retention time from that of NE. Thus, it is highly likely that the interfering peak has been mis-identified as NE in previous studies, providing a reasonable explanation for the high MHBMA3 concentration in urine. The contradiction in the presence of MHBMA3 in urine was also caused by the mis-identification, because the researchers who reported the absence of MHBMA3 were actually detecting NZ. Thus, we clarified the confusion on MHBMA3 in previous studies through correctly identifying the two MHBMA3 isomers. The presence of NE and NZ in human urine warrants further investigations.

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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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