Center for Biological Sequence Analysis, DTU Systems Biology, Building 208, Technical University of Denmark, DK-2800 Lyngby, Denmark.
J Immunol Methods. 2011 Nov 30;374(1-2):26-34. doi: 10.1016/j.jim.2010.10.011. Epub 2010 Oct 31.
In this paper, we describe the methodologies behind three different aspects of the NetMHC family for prediction of MHC class I binding, mainly to HLAs. We have updated the prediction servers, NetMHC-3.2, NetMHCpan-2.2, and a new consensus method, NetMHCcons, which, in their previous versions, have been evaluated to be among the very best performing MHC:peptide binding predictors available. Here we describe the background for these methods, and the rationale behind the different optimization steps implemented in the methods. We go through the practical use of the methods, which are publicly available in the form of relatively fast and simple web interfaces. Furthermore, we will review results obtained in actual epitope discovery projects where previous implementations of the described methods have been used in the initial selection of potential epitopes. Selected potential epitopes were all evaluated experimentally using ex vivo assays.
在本文中,我们描述了 NetMHC 家族三个不同方面的方法学,主要是用于预测 MHC Ⅰ类结合,主要是与 HLA 的结合。我们已经更新了预测服务器,NetMHC-3.2、NetMHCpan-2.2 和一种新的共识方法 NetMHCcons,它们在之前的版本中被评估为性能非常优异的 MHC:肽结合预测器之一。在这里,我们描述了这些方法的背景,以及在方法中实施的不同优化步骤的基本原理。我们将介绍这些方法的实际应用,它们以相对快速和简单的 Web 界面的形式公开提供。此外,我们将回顾在实际的表位发现项目中获得的结果,其中描述的方法的以前实现已用于潜在表位的初步选择。选择的潜在表位都使用体外实验进行了实验评估。