首页> 外文期刊>Journal of chemical theory and computation: JCTC >Variable Regions of Antibodies and T-Cell Receptors May Not Be Sufficient in Molecular Simulations Investigating Binding
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Variable Regions of Antibodies and T-Cell Receptors May Not Be Sufficient in Molecular Simulations Investigating Binding

机译:在调查结合的分子模拟中,抗体和T细胞受体的可变区可能不足以

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Antibodies and T-cell receptors are important proteins of the immune system that share similar structures. Both contain variable and constant regions. Insight into the dynamics of their binding can be provided by computational simulations. For these simulations the constant regions are often removed to save runtime as binding occurs in the variable regions. Here we present the first study to investigate the effect of removing the constant regions from antibodies and T-cell receptors on such simulations. We performed simulations of an antibody/antigen and T-cell receptor/MHC system with and without constant regions using 10 replicas of 100 ns of each of the four setups. We found that simulations without constant regions show significantly different behavior compared to simulations with constant regions. If the constant regions are not included in the simulations alterations in the binding interface hydrogen bonds and even partial unbinding can occur. These results indicate that constant regions should be included, in antibody and T-cell receptor simulations for reliable conclusions to be drawn.
机译:抗体和T细胞受体是免疫系统中具有相似结构的重要蛋白质。两者都包含可变区域和恒定区域。通过计算模拟可以深入了解它们的结合动力学。对于这些模拟,当绑定发生在可变区域中时,通常会删除常量区域以保存运行时。在这里,我们提出了第一项研究,以调查消除抗体和T细胞受体的恒定区域对此类模拟的影响。我们使用四种设置各100纳秒的10个复制品,对抗体/抗原和T细胞受体/MHC系统进行了模拟,包括恒定区域和不恒定区域。我们发现,与具有恒定区域的模拟相比,没有恒定区域的模拟显示出显著不同的行为。如果在模拟中不包括常数区,则结合界面氢键会发生改变,甚至会发生部分解束缚。这些结果表明,在抗体和T细胞受体模拟中,为了得出可靠的结论,应该包括恒定区域。

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