Schein Catherine H, Zhou Bin, Braun Werner
Sealy Center for Structural Biology, Department of Human Biology, Chemistry and Genetics, University of Texas Medical Branch at Galveston, TX, USA.
Virol J. 2005 Apr 21;2:40. doi: 10.1186/1743-422X-2-40.
Flaviviruses, which include Dengue (DV) and West Nile (WN), mutate in response to immune system pressure. Identifying escape mutants, variant progeny that replicate in the presence of neutralizing antibodies, is a common way to identify functionally important residues of viral proteins. However, the mutations typically occur at variable positions on the viral surface that are not essential for viral replication. Methods are needed to determine the true targets of the neutralizing antibodies.
Stereophysicochemical variability plots (SVPs), 3-D images of protein structures colored according to variability, as determined by our PCPMer program, were used to visualize residues conserved in their physical chemical properties (PCPs) near escape mutant positions. The analysis showed 1) that escape mutations in the flavivirus envelope protein are variable residues by our criteria and 2) two escape mutants found at the same position in many flaviviruses sit above clusters of conserved residues from different regions of the linear sequence. Conservation patterns in T-cell epitopes in the NS3- protease suggest a similar mechanism of immune system evasion.
The SVPs add another dimension to structurally defining the binding sites of neutralizing antibodies. They provide a useful aid for determining antigenically important regions and designing vaccines.
包括登革热病毒(DV)和西尼罗河病毒(WN)在内的黄病毒会因免疫系统压力而发生变异。识别逃逸突变体,即在存在中和抗体的情况下仍能复制的变异后代,是鉴定病毒蛋白功能重要残基的常用方法。然而,这些突变通常发生在病毒表面的可变位置,这些位置对病毒复制并非至关重要。因此需要一些方法来确定中和抗体的真正靶点。
立体物理化学变异性图(SVPs),即通过我们的PCPMer程序确定的根据变异性对蛋白质结构进行着色的三维图像,用于可视化逃逸突变体位置附近物理化学性质(PCPs)保守的残基。分析表明:1)按照我们的标准,黄病毒包膜蛋白中的逃逸突变是可变残基;2)在许多黄病毒同一位置发现的两个逃逸突变体位于线性序列不同区域保守残基簇之上。NS3蛋白酶中T细胞表位的保守模式表明存在类似的免疫系统逃避机制。
SVPs为在结构上定义中和抗体的结合位点增加了一个维度。它们为确定抗原重要区域和设计疫苗提供了有用的帮助。