Paper
25 February 2013 Limitations of current fluorescent glucose sensing assays based on competitive binding
Author Affiliations +
Abstract
Competitive binding assays based on the protein Concanavalin A (ConA) have been proposed as potential sensors for continuous glucose monitoring applications. However, ConA-based assays in the literature have primarily displayed a lack of sensitivity or a lack of repeatability in their glucose response. This work explores this apparent trade-off by separating the measured glucose response into the recognition and fluorescence transduction mechanisms. The recognition responses are modeled for typical competing ligands/assays used in the literature, and they are combined with an optimized fluorescence approach to yield expected fluorescent glucose responses. Because aggregation is known to increase the apparent affinity between multivalent ligands and multivalent receptors, preliminary models are generated for assays that were initially optimized with multivalent ligands but increase in affinity over time. These models accurately predict the low sensitivity for monovalent ligands and the lack of repeatability in the responses with multivalent ligands as seen in the literature. This subsequently explains the aforementioned trade-off no matter the optical approach.
© (2013) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Brian M. Cummins, Javier T. Garza, and Gerard L. Coté "Limitations of current fluorescent glucose sensing assays based on competitive binding", Proc. SPIE 8591, Optical Diagnostics and Sensing XIII: Toward Point-of-Care Diagnostics, 859103 (25 February 2013); https://doi.org/10.1117/12.2004564
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Cited by 3 scholarly publications.
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KEYWORDS
Glucose

Luminescence

Anisotropy

Sensors

Receptors

Blood

Proteins

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