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抗原微阵列:描述性化学还是功能免疫组学?

Antigen microarrays: descriptive chemistry or functional immunomics?

机构信息

Research Group of Immunology of the Hungarian Academy of Sciences, Eötvös Loránd University, Budapest 1117, Hungary.

出版信息

Trends Immunol. 2010 Apr;31(4):133-7. doi: 10.1016/j.it.2010.01.004. Epub 2010 Feb 20.

Abstract

Advances in protein microarray technology allow the generation of high content, reliable information about complex, multilevel protein interaction networks. Yet antigen arrays are used mostly only as devices for parallel immune assays describing multitudes of individual binding events. We propose here that the huge amount of immunological information hidden in the plasma of an individual could be better revealed by combining the characterization of antibody binding to target epitopes with improved estimation of effector functions triggered by these binding events. Furthermore, we could generate functional immune profiles characterizing general immune responsiveness of the individual by designing arrays incorporating epitope collections from diverse subsets of antibody targets.

摘要

蛋白质微阵列技术的进步使得能够生成关于复杂的、多层次蛋白质相互作用网络的高信息量、可靠的信息。然而,抗原微阵列主要仅被用作描述大量单个结合事件的平行免疫分析的装置。我们在这里提出,通过将针对靶表位的抗体结合的特征描述与这些结合事件引发的效应功能的改进估计相结合,个体血浆中隐藏的大量免疫学信息可以得到更好的揭示。此外,通过设计包含来自不同抗体靶目标子集的表位集合的阵列,我们可以生成功能免疫谱,以表征个体的一般免疫反应性。

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