journal article·2014-12-10

A Photostable Near-Infrared Fluorescent Tracker with pH-Independent Specificity to Lysosomes for Long Time and Multicolor Imaging

Xinfu Zhang, Chao Wang, Zhuo Han, Yi Xiao

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Abstract

A new boron-dipyrromethene-based lysosome tracker, Lyso-NIR, is facilely synthesized. Besides the intensive near-infrared (NIR) fluorescence and high photostability, Lyso-NIR shows the capability to stably localize in lysosomes, which is independent of the local pH. Lyso-NIR does not have the problematic alkalization effect suffered by the commonly used lysotrackers; thus, it shows ignorable cytotoxicity and slightly affects normal physiological functions of lysosomes. The above advantages of Lyso-NIR make it feasible to track lysosomes' dynamic changes in a relatively long time during the full cellular processes such as apoptosis, heavy metal stimulation, and endocytosis, as is demonstrated in this work. Moreover, Lyso-NIR's narrow NIR emission at 740 nm with a full width at half-maximum smaller than 50 nm makes it easy to avoid the crosstalk with the emissions from other common fluorescent probes, which strengthens Lyso-NIR's competitiveness as a standard lysosome tracker for multicolor bioimaging.
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Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Nanoplatforms for cancer theranostics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Fine Chemicals and School of Life Science and Technology, Dalian University of Technology, 2 Linggong Road, Dalian 116024, P. R. China

Funding

Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China

References (22)

Show source-provided references
1. Luzio J. P. · Nat. Rev. Mol. Cell Biol. · 2007 · 8 · 62210.1038/nrm2217 ↗
2. Saftig P. · Nat. Rev. Mol. Cell Biol. · 2009 · 10 · 62310.1038/nrm2745 ↗
3. Yu L. · Nature · 2010 · 465 · 94210.1038/nature09076 ↗
4. Zhou X. · Biomaterials · 2012 · 33 · 17110.1016/j.biomaterials.2011.09.053 ↗
5. Li Z. · Analyst · 2011 · 136 · 369810.1039/c1an15108h ↗
6. Kroemer G. · Nat. Rev. Cancer · 2005 · 5 · 88610.1038/nrc1738 ↗
7. Kim H. M. · Angew. Chem., Int. Ed. · 2008 · 47 · 223110.1002/anie.200704586 ↗
8. Zhu H. · Chem. Commun. · 2012 · 48 · 1176610.1039/c2cc36785h ↗
9. Haugland, R. P.A Guide to Fluorescent Probes and Labeling Technologies;Invitrogen Corp.:Waltham, MA, 2005, pp580–588.
10. Ohno N. · Immunol. Lett. · 1996 · 110.1016/0165-2478(96)02538-2 ↗
11. Li Z. · Chem. Sci. · 2012 · 3 · 294110.1039/c2sc20733h ↗
12. Farcal L. R. · Nanotoxicology · 2013 · 7 · 109510.3109/17435390.2012.710658 ↗
13. Zhang X. F. · J. Org. Chem. · 2013 · 78 · 915310.1021/jo401379g ↗
14. Dickinson B. C. · J. Am. Chem. Soc. · 2008 · 130 · 963810.1021/ja802355u ↗
15. Chalmers S. · J. Am. Chem. Soc. · 2012 · 134 · 75810.1021/ja2077922 ↗
16. Horobin R. W. · Cell Biol. · 2006 · 126 · 165
17. Wang X. H. · J. Am. Chem. Soc. · 2010 · 132 · 1223710.1021/ja1057423 ↗
18. Horobin R. W. · Biotechnol. Histochem. · 2013 · 88 · 46110.3109/10520295.2013.780635 ↗
19. Horobin R. W. · Biotechnol. Histochem. · 2013 · 88 · 44010.3109/10520295.2013.780634 ↗
20. Poole B. · J. Cell Biol. · 1981 · 90 · 66510.1083/jcb.90.3.665 ↗
21. Gutknecht J. · J. Membr. Biol. · 1981 · 61 · 6110.1007/BF01870753 ↗
22. Hinz B. · Pharm. Res. · 2000 · 17 · 148910.1023/A:1007652908104 ↗