scholarly journals Cadmium-Free Quantum Dots as Fluorescent Labels for Exosomes

Sensors ◽  
2018 ◽  
Vol 18 (10) ◽  
pp. 3308 ◽  
Author(s):  
Garima Dobhal ◽  
Deanna Ayupova ◽  
Geoffry Laufersky ◽  
Zeineb Ayed ◽  
Thomas Nann ◽  
...  

Quantum dots are attractive alternatives to organic fluorophores for the purposes of fluorescent labeling and the detection of biomarkers. They can also be made to specifically target a protein of interest by conjugating biomolecules, such as antibodies. However, the majority of the fluorescent labeling using quantum dots is done using toxic materials such as cadmium or lead due to the well-established synthetic processes for these quantum dots. Here, we demonstrate the use of indium phosphide quantum dots with a zinc sulfide shell for the purposes of labeling and the detection of exosomes derived from the THP-1 cell line (monocyte cell line). Exosomes are nano-sized vesicles that have the potential to be used as biomarkers due to their involvement in complex cell processes. However, the lack of standardized methodology around the detection and analysis of exosomes has made it difficult to detect these membrane-containing vesicles. We targeted a protein that is known to exist on the surface of the exosomes (CD63) using a CD63 antibody. The antibody was conjugated to the quantum dots that were first made water-soluble using a ligand-exchange method. The conjugation was done using carbodiimide coupling, and was confirmed using a range of different methods such as dynamic light scattering, surface plasmon resonance, fluorescent microscopy, and Fourier transform infrared spectroscopy. The conjugation of the quantum dot antibody to the exosomes was further confirmed using similar methods. This demonstrates the potential for the use of a non-toxic conjugate to target nano-sized biomarkers that could be further used for the detection of different diseases.

NANO ◽  
2011 ◽  
Vol 06 (01) ◽  
pp. 75-79 ◽  
Author(s):  
ZHANGSEN YU ◽  
XIYING MA

We report the synthesis of luminescent-doped core/shell quantum dots (QDs) of water-soluble manganese-doped zinc sulfide (ZnS:Mn2+/ZnS) . QDs of ZnS:Mn2+/ZnS were prepared by nucleation doping strategy, with thioglycolic acid (TGA) as stabilizer in aqueous solution. Structure and optical properties of the ZnS:Mn2+/ZnS core/shell quantum dots were characterized by X-ray diffraction and photoluminescence emission spectroscopy. The influence of the synthesis conditions on the luminescent properties of ZnS:Mn2+/ZnS QDs is discussed. Different Mn2+ concentrations, ratios of the TGA/ (Zn+Mn) and thickness of the ZnS shell were used. Results showed that the ZnS:Mn2+/ZnS QDs are water-soluble and have improved fluorescence properties. Therefore, Mn2+ -doped ZnS quantum dots could be potential candidates as fluorescent labeling agents in biology.


2012 ◽  
Vol 519-520 ◽  
pp. 73-77 ◽  
Author(s):  
Jinju Zheng ◽  
Fengmei Gao ◽  
Guodong Wei ◽  
Weiyou Yang

2018 ◽  
Vol 1 (12) ◽  
pp. 6773-6781 ◽  
Author(s):  
Xiaofeng Zan ◽  
Qinzhen Li ◽  
Yiting Pan ◽  
David J. Morris ◽  
Peng Zhang ◽  
...  

Mycoscience ◽  
2010 ◽  
Vol 51 (2) ◽  
pp. 134-138 ◽  
Author(s):  
Noriko Kodama ◽  
Shigeto Mizuno ◽  
Akihiro Asakawa ◽  
Akio Inui ◽  
Hiroaki Nanba

2005 ◽  
Vol 71 (5) ◽  
pp. 2548-2557 ◽  
Author(s):  
J. A. Kloepfer ◽  
R. E. Mielke ◽  
J. L. Nadeau

ABSTRACT Quantum dots (QDs) rendered water soluble for biological applications are usually passivated by several inorganic and/or organic layers in order to increase fluorescence yield. However, these coatings greatly increase the size of the particle, making uptake by microorganisms impossible. We find that adenine- and AMP-conjugated QDs are able to label bacteria only if the particles are <5 nm in diameter. Labeling is dependent upon purine-processing mechanisms, as mutants lacking single enzymes demonstrate a qualitatively different signal than do wild-type strains. This is shown for two example species, one gram negative and one gram positive. Wild-type Bacillus subtilis incubated with QDs conjugated to adenine are strongly fluorescent; very weak signal is seen in mutant cells lacking either adenine deaminase or adenosine phosphoribosyltransferase. Conversely, QD-AMP conjugates label mutant strains more efficiently than the wild type. In Escherichia coli, QD conjugates are taken up most strongly by adenine auxotrophs and are extruded from the cells over a time course of hours. No fluorescent labeling is seen in killed bacteria or in the presence of EDTA or an excess of unlabeled adenine, AMP, or hypoxanthine. Spectroscopy and electron microscopy suggest that QDs of <5 nm can enter the cells whole, probably by means of oxidative damage to the cell membrane which is aided by light.


2013 ◽  
Vol 40 (6) ◽  
pp. 857-861
Author(s):  
Bin ZHAO ◽  
Su-Qing ZHAO ◽  
Li-Hua ZHOU ◽  
Kun ZHANG ◽  
Jun ZHANG
Keyword(s):  

2012 ◽  
Vol 8 (2) ◽  
pp. 202-207 ◽  
Author(s):  
Sonia Bailon-Ruiz ◽  
Luis Alamo-Nole ◽  
Oscar Perales-Perez

2019 ◽  
Vol 2 (10) ◽  
pp. 6135-6143 ◽  
Author(s):  
Haodong Tang ◽  
Jialin Zhong ◽  
Wei Chen ◽  
Kanming Shi ◽  
Guanding Mei ◽  
...  

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