Institute for Research in Biomedicine, Bellinzona, Switzerland.
PLoS One. 2013;8(2):e55561. doi: 10.1371/journal.pone.0055561. Epub 2013 Feb 6.
Antibodies play an increasing pivotal role in both basic research and the biopharmaceutical sector, therefore technology for characterizing and improving their properties through rational engineering is desirable. This is a difficult task thought to require high-resolution x-ray structures, which are not always available. We, instead, use a combination of solution NMR epitope mapping and computational docking to investigate the structure of a human antibody in complex with the four Dengue virus serotypes. Analysis of the resulting models allows us to design several antibody mutants altering its properties in a predictable manner, changing its binding selectivity and ultimately improving its ability to neutralize the virus by up to 40 fold. The successful rational design of antibody mutants is a testament to the accuracy achievable by combining experimental NMR epitope mapping with computational docking and to the possibility of applying it to study antibody/pathogen interactions.
抗体在基础研究和生物制药领域发挥着越来越重要的作用,因此,通过合理的工程技术来表征和改善其特性是可取的。这是一项艰巨的任务,需要高分辨率的 X 射线结构,但并非总是可用。相反,我们使用溶液 NMR 表位作图和计算对接的组合来研究与四种登革热病毒血清型结合的人抗体的结构。对所得模型的分析使我们能够设计几种抗体突变体,以可预测的方式改变其性质,改变其结合选择性,并最终将其中和病毒的能力提高多达 40 倍。抗体突变体的成功合理设计证明了通过将实验 NMR 表位作图与计算对接相结合可以达到的准确性,以及将其应用于研究抗体/病原体相互作用的可能性。