...
首页> 外文期刊>MBio >Lipid-Specific Labeling of Enveloped Viruses with Quantum Dots for Single-Virus Tracking
【24h】

Lipid-Specific Labeling of Enveloped Viruses with Quantum Dots for Single-Virus Tracking

机译:具有单病毒跟踪的量子点的包膜病毒特异性标记

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Quantum dots (QDs) possess optical properties of superbright fluorescence, excellent photostability, narrow emission spectra, and optional colors. Labeled with QDs, single molecules/viruses can be rapidly and continuously imaged for a long time, providing more detailed information than when labeled with other fluorophores. While they are widely used to label proteins in single-molecule-tracking studies, QDs have rarely been used to study virus infection, mainly due to a lack of accepted labeling strategies. Here, we report a general method to mildly and readily label enveloped viruses with QDs. Lipid-biotin conjugates were used to recognize and mark viral lipid membranes, and streptavidin-QD conjugates were used to light them up. Such a method allowed enveloped viruses to be labeled in 2 h with specificity and efficiency up to 99% and 98%, respectively. The intact morphology and the native infectivity of viruses were preserved. With the aid of this QD labeling method, we lit wild-type and mutant Japanese encephalitis viruses up, tracked their infection in living Vero cells, and found that H144A and Q258A substitutions in the envelope protein did not affect the virus intracellular trafficking. The lipid-specific QD labeling method described in this study provides a handy and practical tool to readily “see” the viruses and follow their infection, facilitating the widespread use of single-virus tracking and the uncovering of complex infection mechanisms.
机译:量子点(QDS)具有超观荧光,优异的光稳定性,窄发射光谱和可选颜色的光学性质。用QDS标记,单分子/病毒可以快速且不断地成像很长时间,提供比与其他荧光团标记时的更详细信息。虽然它们被广泛用于标记单分子跟踪研究中的蛋白质,但QD很少被用于研究病毒感染,主要是由于缺乏公认的标签策略。在这里,我们将一般方法与QDS轻微,易于易于标记包裹的病毒。利用脂质 - 生物素缀合物识别并标记病毒脂膜,并使用链霉蛋白-QD缀合物来点亮它们。这种方法允许包膜病毒分别以2小时标记,特异性,效率分别高达99%和98%。保留了含有病毒的完整形态和原生感染性。借助于这种QD标记方法,我们点燃了野生型和突变的日本脑炎病毒,跟踪了它们在活Vero细胞中的感染,发现H144A和Q258A取代在包络蛋白中不影响病毒细胞内运输。本研究中描述的脂质特异性QD标记方法提供了一种方便和实用的工具,以便“参见”病毒并遵循它们的感染,促进单病毒跟踪的广泛使用和揭示复杂感染机制的揭示。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号