Lin Yuxin, Exell Jack, Lin Haoting, Zhang Chen, Welsher Kevin D
Department of Chemistry, Duke University; Durham, North Carolina 27708, United States.
bioRxiv. 2024 May 11:2024.03.14.585070. doi: 10.1101/2024.03.14.585070.
The viral infection process covers a large range of spatiotemporal scales. Tracking the viral infection process with fluorescent labels over long durations while maintaining a fast sampling rate requires bright and highly photostable labels. StayGold is a recently identified green fluorescent protein that has a greater photostability and higher signal intensity under identical illumination conditions as compared to existing fluorescence protein variants. Here, StayGold protein fusions were used to generate virus-like particles (StayGold-VLPs) to achieve hour-long 3D single-virus tracking (SVT) with one thousand localizations per second (kHz sampling rate) in live cells. The expanded photon budget from StayGold protein fusions prolonged the tracking duration, facilitating a comprehensive study of viral trafficking dynamics with high temporal resolution over long timescales. The development of StayGold-VLPs presents a simple and general VLP labeling strategy for better performance in SVT, enabling exponentially more information to be collected from single trajectories and allowing for the future possibility of observing the whole life cycle of a single virus.
病毒感染过程涵盖了广泛的时空尺度。在保持快速采样率的同时,长时间用荧光标记追踪病毒感染过程需要明亮且高度光稳定的标记。StayGold是最近鉴定出的一种绿色荧光蛋白,与现有的荧光蛋白变体相比,在相同光照条件下具有更高的光稳定性和信号强度。在这里,使用StayGold蛋白融合物来生成病毒样颗粒(StayGold-VLPs),以便在活细胞中以每秒一千次定位(kHz采样率)实现长达一小时的三维单病毒追踪(SVT)。StayGold蛋白融合物增加的光子预算延长了追踪持续时间,有助于在长时间尺度上以高时间分辨率对病毒运输动力学进行全面研究。StayGold-VLPs的开发提出了一种简单通用的VLP标记策略,以在SVT中实现更好的性能,能够从单个轨迹中收集指数级更多的信息,并为未来观察单个病毒的整个生命周期提供了可能性。