Protein–Hapten Binding: Challenges and Limitations for In Vitro Skin Sensitization Assays

M. Divkovic, D. Basketter, N. Gilmour, M. Panico, A. Dell, H. Morris, C. Pease
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引用次数: 4

Abstract

In the search for practical alternatives to the use of animals in the predictive identification of chemicals which possess the intrinsic potential to cause sensitization of the skin, for 2 decades attention has been paid to structure–activity relationships. The work has delivered many valuable insights and has even led to the development of useful computer-based systems (e.g., DEREK). However, these efforts have been predicated very largely on an interrogation of how the chemical itself may be reactive (or may become so after metabolic intervention). Scant attention has been paid to the “substrate” with which the chemical must interact, i.e., skin protein. In this review, we consider in detail those actual protein substructures, examining what is known chemically, what may be predicted to occur, and how they can be investigated. Ultimately, understanding of the protein–hapten binding mechanisms in vitro will increase the confidence in sensitization hazard predictions using in silico tools. It could also permit development of a simple in vitro sensitization screen.
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蛋白质-半抗原结合:体外皮肤增敏试验的挑战和局限性
二十年来,为了寻找实际的替代方法,以预测识别具有内在潜在致敏性的化学物质,人们一直关注结构-活性关系。这项工作提供了许多有价值的见解,甚至导致了有用的基于计算机的系统(例如,DEREK)的发展。然而,这些努力在很大程度上是基于对化学物质本身如何具有反应性(或在代谢干预后如何具有反应性)的研究。很少有人注意到化学物质必须与之相互作用的“底物”,即皮肤蛋白质。在这篇综述中,我们详细考虑了这些实际的蛋白质亚结构,检查了化学上已知的,可能预测发生的,以及如何研究它们。最终,在体外了解蛋白质-半抗原结合机制将增加使用硅工具进行致敏危险预测的信心。它也允许开发一种简单的体外致敏筛选。
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