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一种用于实验 TCR-pMHC 动力学常数的统一数学框架。

A unifying mathematical framework for experimental TCR-pMHC kinetic constants.

机构信息

Area of Immunology, Faculty of Biology, and Biomedical Research Center (CINBIO), Universidade de Vigo, Vigo, Spain.

Instituto Gulbenkian de Ciência, Oeiras, Portugal.

出版信息

Sci Rep. 2017 Apr 26;7:46741. doi: 10.1038/srep46741.

Abstract

Receptor binding and triggering are central in Immunology as T cells activated through their T cell receptors (TCR) by protein antigens orchestrate immune responses. In order to understand receptor-ligand interactions, many groups working with different experimental techniques and assays have generated a vast body of knowledge during the last decades. However, in recent years a type of assays, referred to as two-dimensional or membrane-to-membrane, has questioned our current understanding of the role of different kinetic constants (for instance, on- versus off-rate constants) on TCR-ligand interaction and subsequent T cell activation. Here we present a general mathematical framework that provides a unifying umbrella to relate fundamental and effective (or experimentally determined) kinetic constants, as well as describe and compare state-of-the-art experimental methods. Our framework is able to predict the correlations between functional output, such as 1/EC, and effective kinetic constants for a range of different experimental assays (in two and three dimensions). Furthermore, our approach can be applied beyond Immunology, and serve as a "translation method" for the biochemical characterization of receptor-ligand interactions.

摘要

受体结合和触发是免疫学的核心,因为 T 细胞通过其 T 细胞受体 (TCR) 被蛋白质抗原激活,从而协调免疫反应。为了理解受体-配体相互作用,许多使用不同实验技术和测定方法的小组在过去几十年中积累了大量的知识。然而,近年来,一种称为二维或膜对膜的测定方法,对我们目前对不同动力学常数(例如,结合速率常数与解离速率常数)在 TCR-配体相互作用和随后的 T 细胞激活中的作用的理解提出了质疑。在这里,我们提出了一个通用的数学框架,为基本的和有效的(或实验确定的)动力学常数提供了一个统一的概括,并描述和比较了最先进的实验方法。我们的框架能够预测不同实验测定(二维和三维)中功能输出(如 1/EC)和有效动力学常数之间的相关性。此外,我们的方法可以应用于免疫学以外的领域,并作为受体-配体相互作用的生化特征描述的“翻译方法”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ad1/5405415/34e4494b8766/srep46741-f1.jpg

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