Conformation-sensitive antibody-based point-of-care immunosensor for serum Ca2+ using two-dimensional sequential binding reactions
- Authors
- Park, Ji-Na; Paek, Sung-Ho; Kim, Dong-Hyung; Seo, Sung-Min; Lim, Guei-Sam; Kang, Ju-Hee; Paek, Sung-Pil; Cho, Il-Hoon; Paek, Se-Hwan
- Issue Date
- 15-11월-2016
- Publisher
- ELSEVIER ADVANCED TECHNOLOGY
- Keywords
- Conformational change of calcium-binding protein; Conformation-specific antibody; Point-of-care immunosensor for Ca2+; Highly resolved dynamic range; Smartphone-based immunosensor
- Citation
- BIOSENSORS & BIOELECTRONICS, v.85, pp.611 - 617
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIOSENSORS & BIOELECTRONICS
- Volume
- 85
- Start Page
- 611
- End Page
- 617
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/86816
- DOI
- 10.1016/j.bios.2016.05.061
- ISSN
- 0956-5663
- Abstract
- To assess the homeostasis of Ca2+ metabolism, we have developed a rapid immunosensor for ionic calcium using a membrane chromatographic technique. As calcium-binding protein (CBP) is available for the recognition and undergone conformation change upon Ca2+ binding, a monoclonal antibody sensitive to the altered structure of CBP has been employed. The sequential binding scheme was mathematically simulated and shown to match with the experimental results. At the initial stage, the rapid analytical system using lateral flow was constructed by immobilizing the antibody on the immuno-strip nitrocellulose membrane and labeling CBP with colloidal gold as a tracer. A major problem with this system in measuring ionic calcium levels was retarded migration of the gold tracer along the immunostrip. It was conceivable that the divalent cation at a high concentration caused a change in the physical properties of the tracer, resulting in a non-specific interaction with the membrane surface. This problem was circumvented by first eluting a sample containing biotinylated CBP along the immuno-strip and then supplying the gold coupled to streptavidin across the signal generation pad of the strip. The color signal was then generated via biotin-SA linkage and measured using a smartphone-based detector developed in our laboratory. This two-dimensional chromatographic format completed the Ca2+ analysis within 15 min, the analytical performance covered the clinical dynamic range (0.25-2.5 mM) and highly correlated with that of the reference system, i-STAT. These results inspired us to eventually investigate a dual-immunoassay system that measures simultaneously ionic calcium and parathyroid hormone, which regulates the ionic calcium level in serum. This will significantly simplify the current diagnostic protocols, which involve separate devices. (C) 2016 Elsevier B.V. All rights reserved.
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Collections - College of Science and Technology > Department of Biotechnology and Bioinformatics > 1. Journal Articles
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