Rawle Robert J, Webster Elizabeth R, Jelen Marta, Kasson Peter M, Boxer Steven G
Departments of Molecular Physiology and Biological Physics and of Biomedical Engineering, University of Virginia, Charlottesville, Virginia 22908, United States.
Department of Chemistry, Stanford University, Stanford, California 94305, United States.
ACS Cent Sci. 2018 Nov 28;4(11):1503-1510. doi: 10.1021/acscentsci.8b00494. Epub 2018 Oct 12.
The recent spread of Zika virus stimulated extensive research on its structure, pathogenesis, and immunology, but mechanistic study of entry has lagged behind, in part due to the lack of a defined reconstituted system. Here, we report Zika membrane fusion measured using a platform that bypasses these barriers, enabling observation of single-virus fusion kinetics without receptor reconstitution. Surprisingly, target membrane binding and low pH are sufficient to trigger viral hemifusion to liposomes containing only neutral lipids. Second, although the extent of hemifusion strongly depends on pH, hemifusion rates are relatively insensitive to pH. Kinetic analysis shows that an off-pathway state is required to capture this pH-dependence and suggests this may be related to viral inactivation. Our surrogate-receptor approach thus yields new understanding of flaviviral entry mechanisms and should be applicable to many emerging viruses.
寨卡病毒最近的传播刺激了对其结构、发病机制和免疫学的广泛研究,但病毒进入细胞机制的研究却滞后了,部分原因是缺乏明确的重组系统。在此,我们报告了使用一个绕过这些障碍的平台测量寨卡病毒膜融合的情况,该平台能够在不进行受体重组的情况下观察单病毒融合动力学。令人惊讶的是,靶膜结合和低pH值足以触发病毒与仅含中性脂质的脂质体发生半融合。其次,虽然半融合的程度强烈依赖于pH值,但半融合速率对pH值相对不敏感。动力学分析表明,需要一个非经典途径状态来捕捉这种pH依赖性,并表明这可能与病毒失活有关。因此,我们的替代受体方法为黄病毒进入机制带来了新的认识,并且应该适用于许多新兴病毒。