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蛋白质组学过敏原肽/蛋白相互作用分析用于鉴定人类皮肤致敏原。

Proteomic allergen-peptide/protein interaction assay for the identification of human skin sensitizers.

机构信息

Laboratory for Immunology & Proteomics, Department of Dermatology and University Medical Center Mannheim, University of Heidelberg, D-68167 Mannheim, Germany.

出版信息

Toxicol In Vitro. 2013 Apr;27(3):1157-62. doi: 10.1016/j.tiv.2012.08.013. Epub 2012 Aug 17.

DOI:10.1016/j.tiv.2012.08.013
PMID:22926046
Abstract

Modification of proteins by skin sensitizers is a pivotal step in T cell mediated allergic contact dermatitis (ACD). In this process small reactive chemicals interact covalently or non-covalently with cellular or extracellular skin self-proteins or self-peptides to become recognized by the human immune system. Aiming to develop a novel non-animal in vitro test system for predicting sensitization potential of small reactive chemicals in human skin the allergen-peptide/protein interaction assay (APIA) has been developed. By applying modern proteomic technologies together with a target peptide containing all amino acids, the assay permits the profiling of all amino acid specific allergen-peptide interactions. Moreover, potentially crucial allergen-specific Cys-modifications are qualitatively monitored by mass spectrometry and confirmed by a dual peptide approach. Assay conditions chosen mimic the distinct human epidermal reactivity compartments of the skin surface (pH 5.5), stratum basale (pH 6.8), and typical physiological conditions (pH 7.4). An extreme as well as a moderate human contact sensitizer produced Cys-specific mass shifts, whereas a skin irritant did not. Our data indicate that MALDI-MS based and skin-related in vitro technology platforms - like the APIA - are promising tools in developing alternative non-animal allergen assays. This will assist in chemical classification and next generation risk assessment strategies, including REACH and experimental immunotoxicology.

摘要

变应原通过与细胞内或细胞外皮肤自身蛋白或自身肽共价或非共价相互作用,成为被人类免疫系统识别的物质,这是 T 细胞介导的过敏性接触性皮炎(ACD)的关键步骤。本研究旨在开发一种新型的非动物体外测试系统,用于预测小分子反应性化学物质在人类皮肤中的致敏潜力,为此开发了过敏原肽/蛋白相互作用测定法(APIA)。通过应用现代蛋白质组学技术和包含所有氨基酸的靶肽,该测定法可以分析所有氨基酸特异性过敏原肽相互作用。此外,通过质谱法定性监测潜在关键的过敏原特异性半胱氨酸修饰,并通过双肽方法进行确认。选择的测定条件模拟了皮肤表面(pH5.5)、基底细胞层(pH6.8)和典型生理条件(pH7.4)等不同的人类表皮反应性隔室。一种极端和一种中度的人类接触致敏原产生了半胱氨酸特异性的质量转移,而一种皮肤刺激性物质则没有。我们的数据表明,基于 MALDI-MS 和与皮肤相关的体外技术平台(如 APIA)是开发替代动物过敏原测定法的有前途的工具。这将有助于化学分类和下一代风险评估策略,包括 REACH 和实验免疫毒理学。

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