BROWSE

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Author

Madou, Mark
BIO-MEMS Lab
Research Interests
  • Medical Diagnostics

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Investigation into the applicability of the centrifugal microfluidics development of protein-platform for the ligand binding assays incorporating enhanced green fluorescent protein as a fluorescent reporter

Cited 47 times inthomson ciCited 49 times inthomson ci
Title
Investigation into the applicability of the centrifugal microfluidics development of protein-platform for the ligand binding assays incorporating enhanced green fluorescent protein as a fluorescent reporter
Author
Puckett, LGDikici, ELai, SMadou, MarkBachas, LGDaunert, S
Keywords
INDUCED CONFORMATIONAL-CHANGE; LABELED CALMODULIN; DRUG DETECTION; SYSTEMS; DEVICES; PHENOTHIAZINES; DOMAIN
Issue Date
200412
Publisher
AMER CHEMICAL SOC
Citation
ANALYTICAL CHEMISTRY, v.76, no.24, pp.7263 - 7268
Abstract
The incorporation of a protein-ligand binding assay into a centrifugal microfluidics platform is described. The platform itself is a disc-shaped polymer substrate, upon which a series of microfluidic channels and reservoirs have been machined. Centrifugal microfluidics platforms require no internal moving parts, and fluid propulsion is achieved solely through rotation of the disc. Fluid flow is controlled by passive valves, the opening of which is dependent on the angular frequency of the rotating platform, the channel dimensions, and the physical properties of the fluid. To evaluate the effectiveness of incorporating a protein-based assay onto the centrifugal microfluidics analytical platform, a class-selective, homogeneous assay for the detection of phenothiazine antidepressants was employed. This class of drugs is known to bind to calmodulin, a calcium binding protein. Specifically, a fusion protein between calmodulin and enhanced green fluorescent protein was utilized. Calmodulin undergoes a conformational change upon binding to phenothiazines that alters the fluorescence properties of the attached fluorescent protein, which can be correlated to the concentration of the drug present. Another important aspect of this work was to study the efficacy of the platform to perform reconstitution assays. To do this, the biological reagent was dried on the platform and rehydrated to carry out the assay. The ability to prealiquot reagents on the platform should enhance its versatility and portability. The integration of protein-based assays in this platform should be useful in the design of analytical systems for high-throughput screening of pharmaceuticals and clinical diagnostics.
URI
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DOI
http://dx.doi.org/10.1021/ac049758h
ISSN
0003-2700
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