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Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection

BACKGROUND: Rapid diagnosis for time-sensitive illnesses such as stroke, cardiac arrest, and septic shock is essential for successful treatment. Much attention has therefore focused on new strategies for rapid and objective diagnosis, such as Point-of-Care Tests (PoCT) for blood biomarkers. Here we...

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Autores principales: Cohen, Roy, Lata, James P., Lee, Yurim, Hernández, Jean C. Cruz, Nishimura, Nozomi, Schaffer, Chris B., Mukai, Chinatsu, Nelson, Jacquelyn L., Brangman, Sharon A., Agrawal, Yash, Travis, Alexander J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659663/
https://www.ncbi.nlm.nih.gov/pubmed/26605916
http://dx.doi.org/10.1371/journal.pone.0142326
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author Cohen, Roy
Lata, James P.
Lee, Yurim
Hernández, Jean C. Cruz
Nishimura, Nozomi
Schaffer, Chris B.
Mukai, Chinatsu
Nelson, Jacquelyn L.
Brangman, Sharon A.
Agrawal, Yash
Travis, Alexander J.
author_facet Cohen, Roy
Lata, James P.
Lee, Yurim
Hernández, Jean C. Cruz
Nishimura, Nozomi
Schaffer, Chris B.
Mukai, Chinatsu
Nelson, Jacquelyn L.
Brangman, Sharon A.
Agrawal, Yash
Travis, Alexander J.
author_sort Cohen, Roy
collection PubMed
description BACKGROUND: Rapid diagnosis for time-sensitive illnesses such as stroke, cardiac arrest, and septic shock is essential for successful treatment. Much attention has therefore focused on new strategies for rapid and objective diagnosis, such as Point-of-Care Tests (PoCT) for blood biomarkers. Here we use a biomimicry-based approach to demonstrate a new diagnostic platform, based on enzymes tethered to nanoparticles (NPs). As proof of principle, we use oriented immobilization of pyruvate kinase (PK) and luciferase (Luc) on silica NPs to achieve rapid and sensitive detection of neuron-specific enolase (NSE), a clinically relevant biomarker for multiple diseases ranging from acute brain injuries to lung cancer. We hypothesize that an approach capitalizing on the speed and catalytic nature of enzymatic reactions would enable fast and sensitive biomarker detection, suitable for PoCT devices. METHODS AND FINDINGS: We performed in-vitro, animal model, and human subject studies. First, the efficiency of coupled enzyme activities when tethered to NPs versus when in solution was tested, demonstrating a highly sensitive and rapid detection of physiological and pathological concentrations of NSE. Next, in rat stroke models the enzyme-based assay was able in minutes to show a statistically significant increase in NSE levels in samples taken 1 hour before and 0, 1, 3 and 6 hours after occlusion of the distal middle cerebral artery. Finally, using the tethered enzyme assay for detection of NSE in samples from 20 geriatric human patients, we show that our data match well (r = 0.815) with the current gold standard for biomarker detection, ELISA—with a major difference being that we achieve detection in 10 minutes as opposed to the several hours required for traditional ELISA. CONCLUSIONS: Oriented enzyme immobilization conferred more efficient coupled activity, and thus higher assay sensitivity, than non-tethered enzymes. Together, our findings provide proof of concept for using oriented immobilization of active enzymes on NPs as the basis for a highly rapid and sensitive biomarker detection platform. This addresses a key challenge in developing a PoCT platform for time sensitive and difficult to diagnose pathologies.
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spelling pubmed-46596632015-12-02 Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection Cohen, Roy Lata, James P. Lee, Yurim Hernández, Jean C. Cruz Nishimura, Nozomi Schaffer, Chris B. Mukai, Chinatsu Nelson, Jacquelyn L. Brangman, Sharon A. Agrawal, Yash Travis, Alexander J. PLoS One Research Article BACKGROUND: Rapid diagnosis for time-sensitive illnesses such as stroke, cardiac arrest, and septic shock is essential for successful treatment. Much attention has therefore focused on new strategies for rapid and objective diagnosis, such as Point-of-Care Tests (PoCT) for blood biomarkers. Here we use a biomimicry-based approach to demonstrate a new diagnostic platform, based on enzymes tethered to nanoparticles (NPs). As proof of principle, we use oriented immobilization of pyruvate kinase (PK) and luciferase (Luc) on silica NPs to achieve rapid and sensitive detection of neuron-specific enolase (NSE), a clinically relevant biomarker for multiple diseases ranging from acute brain injuries to lung cancer. We hypothesize that an approach capitalizing on the speed and catalytic nature of enzymatic reactions would enable fast and sensitive biomarker detection, suitable for PoCT devices. METHODS AND FINDINGS: We performed in-vitro, animal model, and human subject studies. First, the efficiency of coupled enzyme activities when tethered to NPs versus when in solution was tested, demonstrating a highly sensitive and rapid detection of physiological and pathological concentrations of NSE. Next, in rat stroke models the enzyme-based assay was able in minutes to show a statistically significant increase in NSE levels in samples taken 1 hour before and 0, 1, 3 and 6 hours after occlusion of the distal middle cerebral artery. Finally, using the tethered enzyme assay for detection of NSE in samples from 20 geriatric human patients, we show that our data match well (r = 0.815) with the current gold standard for biomarker detection, ELISA—with a major difference being that we achieve detection in 10 minutes as opposed to the several hours required for traditional ELISA. CONCLUSIONS: Oriented enzyme immobilization conferred more efficient coupled activity, and thus higher assay sensitivity, than non-tethered enzymes. Together, our findings provide proof of concept for using oriented immobilization of active enzymes on NPs as the basis for a highly rapid and sensitive biomarker detection platform. This addresses a key challenge in developing a PoCT platform for time sensitive and difficult to diagnose pathologies. Public Library of Science 2015-11-25 /pmc/articles/PMC4659663/ /pubmed/26605916 http://dx.doi.org/10.1371/journal.pone.0142326 Text en © 2015 Cohen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cohen, Roy
Lata, James P.
Lee, Yurim
Hernández, Jean C. Cruz
Nishimura, Nozomi
Schaffer, Chris B.
Mukai, Chinatsu
Nelson, Jacquelyn L.
Brangman, Sharon A.
Agrawal, Yash
Travis, Alexander J.
Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection
title Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection
title_full Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection
title_fullStr Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection
title_full_unstemmed Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection
title_short Use of Tethered Enzymes as a Platform Technology for Rapid Analyte Detection
title_sort use of tethered enzymes as a platform technology for rapid analyte detection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659663/
https://www.ncbi.nlm.nih.gov/pubmed/26605916
http://dx.doi.org/10.1371/journal.pone.0142326
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