scholarly journals Modular fluorescent nanoparticle DNA probes for detection of peptides and proteins

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Cassandra M. Stawicki ◽  
Torri E. Rinker ◽  
Markus Burns ◽  
Sonal S. Tonapi ◽  
Rachel P. Galimidi ◽  
...  

AbstractFluorescently labeled antibody and aptamer probes are used in biological studies to characterize binding interactions, measure concentrations of analytes, and sort cells. Fluorescent nanoparticle labels offer an excellent alternative to standard fluorescent labeling strategies due to their enhanced brightness, stability and multivalency; however, challenges in functionalization and characterization have impeded their use. This work introduces a straightforward approach for preparation of fluorescent nanoparticle probes using commercially available reagents and common laboratory equipment. Fluorescent polystyrene nanoparticles, Thermo Fisher Scientific FluoSpheres, were used in these proof-of-principle studies. Particle passivation was achieved by covalent attachment of amine-PEG-azide to carboxylated particles, neutralizing the surface charge from − 43 to − 15 mV. A conjugation-annealing handle and DNA aptamer probe were attached to the azide-PEG nanoparticle surface either through reaction of pre-annealed handle and probe or through a stepwise reaction of the nanoparticles with the handle followed by aptamer annealing. Nanoparticles functionalized with DNA aptamers targeting histidine tags and VEGF protein had high affinity (EC50s ranging from 3 to 12 nM) and specificity, and were more stable than conventional labels. This protocol for preparation of nanoparticle probes relies solely on commercially available reagents and common equipment, breaking down the barriers to use nanoparticles in biological experiments.

2021 ◽  
Author(s):  
Cassandra M. Stawicki ◽  
Torri E. Rinker ◽  
Markus Burns ◽  
Sonal S. Tonapi ◽  
Rachel P. Galimidi ◽  
...  

Fluorescently labeled antibody and aptamer probes are used in biological studies to characterize binding interactions, measure concentrations of analytes, and sort cells. Fluorescent nanoparticle labels offer an excellent alternative to standard fluorescent labeling strategies due to their enhanced brightness, stability and multivalency; however, challenges in functionalization and characterization have impeded their use. This work introduces a straightforward approach for preparation of fluorescent nanoparticle probes using commercially available reagents and common laboratory equipment. Fluorescent polystyrene nanoparticles, Thermo Fisher FluoSpheres™, were used in proof-of-principle studies. Particle passivation was achieved by covalent attachment of amine-PEG-azide to carboxylated particles, neutralizing the surface charge from -47 to -17 mV. A conjugation-annealing handle and DNA aptamer probe was attached to the azide-PEG nanoparticle surface either through reaction of pre-annealed handle and probe or through a stepwise reaction of the nanoparticles with the handle followed by aptamer annealing. Nanoparticles functionalized with DNA aptamers targeting histidine tags and VEGF protein had high affinity (EC50s ranging from 2-7 nM) and specificity, and were more stable than conventional labels. This protocol for preparation of nanoparticle probes relies solely on commercially available reagents and common equipment, breaking down the barriers to use of nanoparticles in biological experiments.


2021 ◽  
Vol 179 ◽  
pp. 113084 ◽  
Author(s):  
Sylvie Egloff ◽  
Nina Melnychuk ◽  
Andreas Reisch ◽  
Sophie Martin ◽  
Andrey S. Klymchenko

2015 ◽  
Vol 87 (3) ◽  
pp. 1919-1924 ◽  
Author(s):  
Ying Pu ◽  
Zhenxu Liu ◽  
Yi Lu ◽  
Peng Yuan ◽  
Jun Liu ◽  
...  
Keyword(s):  

2008 ◽  
Vol 16 (1) ◽  
pp. 12-15
Author(s):  
Suk J. Hong ◽  
Richik N. Ghosh

High-content screening (HCS) and other quantitative cellular imaging assay methods that use fluorescence microscopy require effective fluorescent labeling and identification of the target cell(s). Fluorescent probes that stain cells as the primary objects are used to identify and count individual cells, as well as to define the region(s) of each cell to which target-specific image analysis is applied. For this purpose, the primary object can be a major component of the cell, such as the nucleus or a large organelle, or the whole cell itself. When the whole cell is the primary object, a high-quality cell stain is needed to delineate the intact cell from bordering cells without also interfering in target-specific detection and analysis. Thermo Scientific Cellomics ® Whole Cell Stains (Thermo Fisher Scientific Inc., Rockford, Ill.), available in blue, green, orange and red, provides image staining and the ability to quantify the whole cell volume in HCS and fluorescence microscopy assays.


2005 ◽  
Vol 4 (6) ◽  
pp. 593-602 ◽  
Author(s):  
Swadeshmukul Santra ◽  
Debamitra Dutta ◽  
Glenn A. Walter ◽  
Brij M. Moudgil

Optical imaging technique has strong potential for sensitive cancer diagnosis, particularly at the early stage of cancer development. This is a sensitive, non-invasive, non-ionizing (clinically safe) and relatively inexpensive technique. Cancer imaging with optical technique however greatly relies upon the use of sensitive and stable optical probes. Unlike the traditional organic fluorescent probes, fluorescent nanoparticle probes such as dye-doped nanoparticles and quantum dots (Qdots) are bright and photostable. Fluorescent nanoparticle probes are shown to be very effective for sensitive cancer imaging with greater success in the cellular level. However, cancer imaging in an in vivo setup has been recently realized. There are several challenges in developing fluorescent nanoparticle probes for in vivo cancer imaging applications. In this review, we will discuss various aspects of nanoparticle design, synthesis, surface functionalization for bioconjugation and cancer cell targeting. A brief overview of in vivo cancer imaging with Qdots will also be presented.


2009 ◽  
Vol 55 (4) ◽  
pp. 670-683 ◽  
Author(s):  
Larry J Kricka ◽  
Paolo Fortina

Abstract Background: The inherent fluorescent properties of nucleosides, nucleotides, and nucleic acids are limited, and thus the need has arisen for fluorescent labeling of these molecules for a variety of analytical applications. Content: This review traces the analytical ancestry of fluorescent labeling of nucleosides, nucleotides, and nucleic acids, with an emphasis on the first to publish or patent. The scope of labeling includes (a) direct labeling by covalent labeling of nucleic acids with a fluorescent label or noncovalent binding or intercalation of a fluorescent dye to nucleic acids and (b) indirect labeling via covalent attachment of a secondary label to a nucleic acid, and then binding this to a fluorescently labeled ligand binder. An alternative indirect strategy involves binding of a nucleic acid to a nucleic acid binder molecule (e.g., antibody, antibiotic, histone, antibody, nuclease) that is labeled with a fluorophore. Fluorescent labels for nucleic acids include organic fluorescent dyes, metal chelates, carbon nanotubes, quantum dots, gold particles, and fluorescent minerals. Summary: Fluorescently labeled nucleosides, nucleotides, and nucleic acids are important types of reagents for biological assay methods and underpin current methods of chromosome analysis, gel staining, DNA sequencing and quantitative PCR. Although these methods use predominantly organic fluorophores, new types of particulate fluorophores in the form of nanoparticles, nanorods, and nanotubes may provide the basis of a new generation of fluorescent labels and nucleic acid detection methods.


2017 ◽  
Vol 872 ◽  
pp. 173-177 ◽  
Author(s):  
Wei Xiong ◽  
Su Fang Wu ◽  
Fu Sheng Liao ◽  
Nian Hong ◽  
Hao Fan ◽  
...  

Codeine (3-methylmorphine) is an opiate that is widely used to treat mild or moderate pain and cough suppression. It is the second predominant alkaloid in opium with a mild sedative effect. In the present study, we describe an electrochemical sensor for codeine detection by using the DNA aptamers against codeine. In the sensing protocol, a dually-labeled DNA aptamer probe was designed to be labeled at one end with HS, and at its another end with dabcyl as an electrochemical tag to produce electrochemical signal via recognization occurrence. One special electrochemical marker was prepared by modifying ZnS nanoparticle with-cyclodextrins (ab. ZnS-CDs), which employed as electrochemical signal provider and would conjunct with the codeine probe modified electrode through the host–guest recognition of CDs to dabcyl. With codeine adding, aptamer folding allows the ZnS-CDs into soultion that caused an increase of current signal. This sensor has the ability to detect 37pM codeine. Our study demonstrates that the biosensor has good specificity and stability. It can be used to detect codeine.


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