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Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component
BACKGROUND: Quantum dot (QD)-based single virus tracking has become a powerful tool for dissecting virus infection mechanism. However, only virus behaviors at the early stage of retrograde trafficking have been dynamically tracked so far. Monitoring of comprehensive virus retrograde transportation r...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420409/ https://www.ncbi.nlm.nih.gov/pubmed/28477617 http://dx.doi.org/10.1186/s12951-017-0270-9 |
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author | Wen, Li Zheng, Zhen-Hua Liu, An-An Lv, Cheng Zhang, Li-Juan Ao, Jian Zhang, Zhi-Ling Wang, Han-Zhong Lin, Yi Pang, Dai-Wen |
author_facet | Wen, Li Zheng, Zhen-Hua Liu, An-An Lv, Cheng Zhang, Li-Juan Ao, Jian Zhang, Zhi-Ling Wang, Han-Zhong Lin, Yi Pang, Dai-Wen |
author_sort | Wen, Li |
collection | PubMed |
description | BACKGROUND: Quantum dot (QD)-based single virus tracking has become a powerful tool for dissecting virus infection mechanism. However, only virus behaviors at the early stage of retrograde trafficking have been dynamically tracked so far. Monitoring of comprehensive virus retrograde transportation remains a challenge. RESULTS: Based on the superior fluorescence properties of QDs and their labeling of virus internal component, the dynamic interactions between baculoviruses and all key transportation-related cellular structures, including vesicles, acidic endosomes, actins, nuclear pores and nuclei, were visualized at the single-virus level. Detailed scenarios and dynamic information were provided for these critical interaction processes. CONCLUSIONS: A comprehensive model of baculovirus retrograde trafficking involving virus endocytosis, fusion with acidic endosome, translocation to nuclear periphery, internalization into nucleus, and arriving at the destination in nucleus was proposed. Thus the whole retrograde transportation of baculovirus in live host cells was elucidated at the single-virus level for the first time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-017-0270-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5420409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54204092017-05-08 Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component Wen, Li Zheng, Zhen-Hua Liu, An-An Lv, Cheng Zhang, Li-Juan Ao, Jian Zhang, Zhi-Ling Wang, Han-Zhong Lin, Yi Pang, Dai-Wen J Nanobiotechnology Short Communication BACKGROUND: Quantum dot (QD)-based single virus tracking has become a powerful tool for dissecting virus infection mechanism. However, only virus behaviors at the early stage of retrograde trafficking have been dynamically tracked so far. Monitoring of comprehensive virus retrograde transportation remains a challenge. RESULTS: Based on the superior fluorescence properties of QDs and their labeling of virus internal component, the dynamic interactions between baculoviruses and all key transportation-related cellular structures, including vesicles, acidic endosomes, actins, nuclear pores and nuclei, were visualized at the single-virus level. Detailed scenarios and dynamic information were provided for these critical interaction processes. CONCLUSIONS: A comprehensive model of baculovirus retrograde trafficking involving virus endocytosis, fusion with acidic endosome, translocation to nuclear periphery, internalization into nucleus, and arriving at the destination in nucleus was proposed. Thus the whole retrograde transportation of baculovirus in live host cells was elucidated at the single-virus level for the first time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12951-017-0270-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-06 /pmc/articles/PMC5420409/ /pubmed/28477617 http://dx.doi.org/10.1186/s12951-017-0270-9 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Communication Wen, Li Zheng, Zhen-Hua Liu, An-An Lv, Cheng Zhang, Li-Juan Ao, Jian Zhang, Zhi-Ling Wang, Han-Zhong Lin, Yi Pang, Dai-Wen Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
title | Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
title_full | Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
title_fullStr | Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
title_full_unstemmed | Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
title_short | Tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
title_sort | tracking single baculovirus retrograde transportation in host cell via quantum dot-labeling of virus internal component |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420409/ https://www.ncbi.nlm.nih.gov/pubmed/28477617 http://dx.doi.org/10.1186/s12951-017-0270-9 |
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