Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
David Geffen School of Medicine at University of California, Los Angeles, CA 90095, USA.
Viruses. 2021 Oct 19;13(10):2106. doi: 10.3390/v13102106.
The H1N1 pandemic of 2009-2010, MERS epidemic of 2012, Ebola epidemics of 2013-2016 and 2018-2020, Zika epidemic of 2015-2016, and COVID-19 pandemic of 2019-2021, are recent examples in the long history of epidemics that demonstrate the enormous global impact of viral infection. The rapid development of safe and effective vaccines and therapeutics has proven vital to reducing morbidity and mortality from newly emerging viruses. Structural biology methods can be used to determine how antibodies elicited during infection or vaccination target viral proteins and identify viral epitopes that correlate with potent neutralization. Here we review how structural and molecular biology approaches have contributed to our understanding of antibody recognition of pathogenic viruses, specifically HIV-1, SARS-CoV-2, and Zika. Determining structural correlates of neutralization of viruses has guided the design of vaccines, monoclonal antibodies, and small molecule inhibitors in response to the global threat of viral epidemics.
2009-2010 年的 H1N1 大流行、2012 年的 MERS 疫情、2013-2016 年和 2018-2020 年的埃博拉疫情、2015-2016 年的寨卡疫情以及 2019-2021 年的 COVID-19 大流行,是病毒感染在传染病漫长历史中造成巨大全球影响的最近例证。安全有效疫苗和疗法的快速发展已被证明对降低新出现病毒的发病率和死亡率至关重要。结构生物学方法可用于确定感染或接种疫苗期间产生的抗体针对病毒蛋白的方式,并确定与有效中和作用相关的病毒表位。本文综述了结构和分子生物学方法如何帮助我们了解致病性病毒(特别是 HIV-1、SARS-CoV-2 和寨卡病毒)抗体的识别。确定病毒中和作用的结构相关性为应对全球病毒流行的威胁,设计疫苗、单克隆抗体和小分子抑制剂提供了指导。