scholarly journals Site-Specific Labeling of Enveloped Viruses with Quantum Dots for Single Virus Tracking

ACS Nano ◽  
2008 ◽  
Vol 2 (8) ◽  
pp. 1553-1562 ◽  
Author(s):  
Kye-Il Joo ◽  
Yuning Lei ◽  
Chi-Lin Lee ◽  
Jonathon Lo ◽  
Jiansong Xie ◽  
...  
mBio ◽  
2020 ◽  
Vol 11 (3) ◽  
Author(s):  
Li-Juan Zhang ◽  
Shaobo Wang ◽  
Li Xia ◽  
Cheng Lv ◽  
Hong-Wu Tang ◽  
...  

ABSTRACT 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. IMPORTANCE Virus infection in host cells is a complex process comprising a large number of dynamic molecular events. Single-virus tracking is a versatile technique to study these events. To perform this technique, viruses must be fluorescently labeled to be visible to fluorescence microscopes. The quantum dot is a kind of fluorescent tag that has many unique optical properties. It has been widely used to label proteins in single-molecule-tracking studies but rarely used to study virus infection, mainly due to the lack of an accepted labeling method. In this study, we developed a lipid-specific method to readily, mildly, specifically, and efficiently label enveloped viruses with quantum dots by recognizing viral envelope lipids with lipid-biotin conjugates and recognizing these lipid-biotin conjugates with streptavidin-quantum dot conjugates. It is not only applicable to normal viruses, but also competent to label the key protein-mutated viruses and the inactivated highly virulent viruses, providing a powerful tool for single-virus tracking.


Nano Letters ◽  
2020 ◽  
Vol 20 (4) ◽  
pp. 2931-2931
Author(s):  
Yong-Bo Yang ◽  
Yan-Dong Tang ◽  
Yue Hu ◽  
Fang Yu ◽  
Jun-Yao Xiong ◽  
...  

Nano Letters ◽  
2018 ◽  
Vol 18 (12) ◽  
pp. 7457-7468 ◽  
Author(s):  
Qin Li ◽  
Wen Yin ◽  
Wei Li ◽  
Zhiping Zhang ◽  
Xiaowei Zhang ◽  
...  

2020 ◽  
Author(s):  
Li-Juan Zhang ◽  
Shaobo Wang ◽  
Li Xia ◽  
Cheng Lv ◽  
Hong-Wu Tang ◽  
...  

AbstractQuantum 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 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 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 (SA)-QD conjugates were used to light them up. Such a method allowed enveloped viruses to be labeled in 2 hours with specificity and efficiency up to 99% and 98%. The intact morphology and the native infectivity of viruses could be furthest preserved. With the aid of this QD labeling method, we lit wild-type (WT) and mutant Japanese encephalitis virus (JEV) up, tracked their infection in living Vero cells, and found that H144A and Q258A substitutions in the envelope (E) protein didn’t 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.Author summaryVirus infection in host cells is a complex process comprising a large number of dynamic molecular events. Single-virus tracking is a versatile technique to study these events. To perform this technique, viruses must be fluorescently labeled to be visible to fluorescence microscopes. Quantum dot is a kind of fluorescent tags that has many unique optical properties. It has been widely used to label proteins in single-molecule tracking studies, but rarely used to study virus infection, mainly due to lack of accepted labeling method. In this study, we developed a lipid-specific method to readily, mildly, specifically, and efficiently label enveloped viruses with quantum dots by recognizing viral envelope lipids with lipid-biotin conjugates and recognizing these lipid-biotin conjugates with streptavidin-quantum dot conjugates. Such a method is superior to the commonly used DiD/DiO labeling and the other QD labeling methods. It is not only applicable to normal viruses, but also competent to label the key protein-mutated viruses and the inactivated high virulent viruses, providing a powerful tool for single-virus tracking.


Nano Letters ◽  
2020 ◽  
Vol 20 (2) ◽  
pp. 1417-1427 ◽  
Author(s):  
Yong-Bo Yang ◽  
Yan-Dong Tang ◽  
Yue Hu ◽  
Fang Yu ◽  
Jun-Yao Xiong ◽  
...  

Biomaterials ◽  
2014 ◽  
Vol 35 (7) ◽  
pp. 2295-2301 ◽  
Author(s):  
Li Wen ◽  
Yi Lin ◽  
Zhen-Hua Zheng ◽  
Zhi-Ling Zhang ◽  
Li-Juan Zhang ◽  
...  

2006 ◽  
Vol 118 (30) ◽  
pp. 5058-5062 ◽  
Author(s):  
Yan Zhang ◽  
Min-kyung So ◽  
Andreas M. Loening ◽  
Hequan Yao ◽  
Sanjiv S. Gambhir ◽  
...  
Keyword(s):  

2008 ◽  
pp. 5927 ◽  
Author(s):  
Murat Sunbul ◽  
Michelle Yen ◽  
Yekui Zou ◽  
Jun Yin

2019 ◽  
Vol 35 (4) ◽  
pp. 407-416
Author(s):  
Zhenpu Liang ◽  
Pengjuan Li ◽  
Caiping Wang ◽  
Deepali Singh ◽  
Xiaoxia Zhang

Biomaterials ◽  
2010 ◽  
Vol 31 (32) ◽  
pp. 8362-8370 ◽  
Author(s):  
Min Xie ◽  
Kan Luo ◽  
Bi-Hai Huang ◽  
Shu-Lin Liu ◽  
Jun Hu ◽  
...  

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