Development of Bright and Biocompatible Nanoruby and Its Application to Background-Free Time-Gated Imaging of G-Protein-Coupled Receptors

被引:16
|
作者
Sreenivasan, Varun K. A. [1 ,2 ,10 ]
Razali, Wan Aizuddin Wan [1 ,2 ,8 ]
Zhang, Kai [1 ,2 ,9 ]
Pillai, Rashmi R. [1 ,2 ]
Sain, Avishkar [4 ,5 ]
Denkova, Denitza [1 ,2 ]
Santiago, Marina [3 ]
Brown, Hannah [4 ,5 ]
Thompson, Jeremy [4 ,5 ]
Connor, Mark [3 ]
Goldys, Ewa M. [1 ,2 ]
Zvyagin, Andrei V. [1 ,2 ,6 ,7 ]
机构
[1] Macquarie Univ, Dept Phys & Astron, N Ryde, NSW 2122, Australia
[2] Macquarie Univ, Ctr Nanoscale BioPhoton, N Ryde, NSW 2122, Australia
[3] Macquarie Univ, Dept Biomed Sci, N Ryde, NSW 2122, Australia
[4] Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia
[5] Univ Adelaide, Ctr Nanoscale BioPhoton, Adelaide Med Sch, Adelaide, SA, Australia
[6] Sechenov First Moscow State Univ, Inst Mol Med, Moscow 119991, Russia
[7] Lobachevsky Nizhny Novgorod State Univ, Inst Biol & Biomed, Nizhnii Novgorod 603022, Russia
[8] Univ Teknol MARA Cawangan Pahang, Fac Sci Appl, Jengka 26400, Pahang, Malaysia
[9] Jilin Univ, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China
[10] Univ New South Wales, Single Mol Sci, Level 3 Lowy, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会; 俄罗斯科学基金会;
关键词
nanoruby; opioid; GPCR; time-gated microscopy; single-particle; COLLOIDAL ALUMINA PARTICLES; NANOPARTICLES; TRAFFICKING; ALPHA-AL2O3; ACTIVATION; MICROSCOPY; POWDERS; MEDIA;
D O I
10.1021/acsami.7b12665
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
At the forefront of developing fluorescent probes for biological imaging applications are enhancements aimed at increasing their brightness, contrast, and photostability, especially toward demanding applications of single-molecule detection. In comparison with existing probes, nanorubies exhibit unlimited photostability and a long emission lifetime (similar to 4 ms), which enable continuous imaging at single-particle sensitivity in highly scattering and fluorescent biological specimens. However, their wide application as fluorescence probes has so far been hindered by the absence of facile methods for scaled-up high-volume production and molecularly specific targeting. The present work encompasses the large-scale production of colloidally stable nanoruby particles, the demonstration of their biofunctionality and negligible cytotoxicity, as well as the validation of its use for targeted biomolecular imaging. In addition, optical characteristics of nanorubies are found to be comparable or superior to those of state-of-the-art quantum dots. Protocols of reproducible and robust coupling of functional proteins to the nanoruby surface are also presented. As an example, NeutrAvidin-coupled nanoruby show excellent affinity and specificity to mu-opioid receptors in fixed and live cells, allowing wide-field imaging of G-protein coupled receptors with single-particle sensitivity.
引用
收藏
页码:39197 / 39208
页数:12
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