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Dual-functional protein for one-step production of a soluble and targeted fluorescent dye
Low water solubility and poor selectivity are two fundamental limitations that compromise applications of near-infrared (NIR) fluorescent probes. Methods: Here, a simple strategy that can resolve these problems simultaneously was developed by using a novel hybrid protein named RGD-HFBI that is produ...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996361/ https://www.ncbi.nlm.nih.gov/pubmed/29896306 http://dx.doi.org/10.7150/thno.24613 |
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author | Xiao, Yunjie Zhang, Qian Wang, Yanyan Wang, Bin Sun, Fengnan Han, Ziyu Feng, Yaqing Yang, Haitao Meng, Shuxian Wang, Zefang |
author_facet | Xiao, Yunjie Zhang, Qian Wang, Yanyan Wang, Bin Sun, Fengnan Han, Ziyu Feng, Yaqing Yang, Haitao Meng, Shuxian Wang, Zefang |
author_sort | Xiao, Yunjie |
collection | PubMed |
description | Low water solubility and poor selectivity are two fundamental limitations that compromise applications of near-infrared (NIR) fluorescent probes. Methods: Here, a simple strategy that can resolve these problems simultaneously was developed by using a novel hybrid protein named RGD-HFBI that is produced by fusion of hydrophobin HFBI and arginine-glycine-aspartic acid (RGD) peptide. This unique hybrid protein inherits self-assembly and targeting functions from HFBI and RGD peptide respectively. Results: Boron-dipyrromethene (BODIPY) used as a model NIR dye can be efficiently dispersed in the RGD-HFBI solution by simple mixing and sonication for 30 min. The data shows that self-assembled RGD-HFBI forms a protein nanocage by using the BODIPY as the assembly template. Cell uptake assay proves that RGD-HFBI/BODIPY can efficiently stain αvβ3 integrin-positive cancer cells. Finally, in vivo affinity tests fully demonstrate that the soluble RGD-HFBI/BODIPY complex selectively targets and labels tumor sites of tumor-bearing mice due to the high selectivity of the RGD peptide. Conclusion: Our one-step strategy using dual-functional RGD-HFBI opens a novel route to generate soluble and targeted NIR fluorescent dyes in a very simple and efficient way and may be developed as a general strategy to broaden their applications. |
format | Online Article Text |
id | pubmed-5996361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-59963612018-06-12 Dual-functional protein for one-step production of a soluble and targeted fluorescent dye Xiao, Yunjie Zhang, Qian Wang, Yanyan Wang, Bin Sun, Fengnan Han, Ziyu Feng, Yaqing Yang, Haitao Meng, Shuxian Wang, Zefang Theranostics Research Paper Low water solubility and poor selectivity are two fundamental limitations that compromise applications of near-infrared (NIR) fluorescent probes. Methods: Here, a simple strategy that can resolve these problems simultaneously was developed by using a novel hybrid protein named RGD-HFBI that is produced by fusion of hydrophobin HFBI and arginine-glycine-aspartic acid (RGD) peptide. This unique hybrid protein inherits self-assembly and targeting functions from HFBI and RGD peptide respectively. Results: Boron-dipyrromethene (BODIPY) used as a model NIR dye can be efficiently dispersed in the RGD-HFBI solution by simple mixing and sonication for 30 min. The data shows that self-assembled RGD-HFBI forms a protein nanocage by using the BODIPY as the assembly template. Cell uptake assay proves that RGD-HFBI/BODIPY can efficiently stain αvβ3 integrin-positive cancer cells. Finally, in vivo affinity tests fully demonstrate that the soluble RGD-HFBI/BODIPY complex selectively targets and labels tumor sites of tumor-bearing mice due to the high selectivity of the RGD peptide. Conclusion: Our one-step strategy using dual-functional RGD-HFBI opens a novel route to generate soluble and targeted NIR fluorescent dyes in a very simple and efficient way and may be developed as a general strategy to broaden their applications. Ivyspring International Publisher 2018-04-30 /pmc/articles/PMC5996361/ /pubmed/29896306 http://dx.doi.org/10.7150/thno.24613 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Xiao, Yunjie Zhang, Qian Wang, Yanyan Wang, Bin Sun, Fengnan Han, Ziyu Feng, Yaqing Yang, Haitao Meng, Shuxian Wang, Zefang Dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
title | Dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
title_full | Dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
title_fullStr | Dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
title_full_unstemmed | Dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
title_short | Dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
title_sort | dual-functional protein for one-step production of a soluble and targeted fluorescent dye |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5996361/ https://www.ncbi.nlm.nih.gov/pubmed/29896306 http://dx.doi.org/10.7150/thno.24613 |
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