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Enzyme Molecules in Solitary Confinement

Large arrays of homogeneous microwells each defining a femtoliter volume are a versatile platform for monitoring the substrate turnover of many individual enzyme molecules in parallel. The high degree of parallelization enables the analysis of a statistically representative enzyme population. Enclos...

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Detalles Bibliográficos
Autores principales: Liebherr, Raphaela B., Gorris, Hans H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271441/
https://www.ncbi.nlm.nih.gov/pubmed/25221867
http://dx.doi.org/10.3390/molecules190914417
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author Liebherr, Raphaela B.
Gorris, Hans H.
author_facet Liebherr, Raphaela B.
Gorris, Hans H.
author_sort Liebherr, Raphaela B.
collection PubMed
description Large arrays of homogeneous microwells each defining a femtoliter volume are a versatile platform for monitoring the substrate turnover of many individual enzyme molecules in parallel. The high degree of parallelization enables the analysis of a statistically representative enzyme population. Enclosing individual enzyme molecules in microwells does not require any surface immobilization step and enables the kinetic investigation of enzymes free in solution. This review describes various microwell array formats and explores their applications for the detection and investigation of single enzyme molecules. The development of new fabrication techniques and sensitive detection methods drives the field of single molecule enzymology. Here, we introduce recent progress in single enzyme molecule analysis in microwell arrays and discuss the challenges and opportunities.
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spelling pubmed-62714412018-12-27 Enzyme Molecules in Solitary Confinement Liebherr, Raphaela B. Gorris, Hans H. Molecules Review Large arrays of homogeneous microwells each defining a femtoliter volume are a versatile platform for monitoring the substrate turnover of many individual enzyme molecules in parallel. The high degree of parallelization enables the analysis of a statistically representative enzyme population. Enclosing individual enzyme molecules in microwells does not require any surface immobilization step and enables the kinetic investigation of enzymes free in solution. This review describes various microwell array formats and explores their applications for the detection and investigation of single enzyme molecules. The development of new fabrication techniques and sensitive detection methods drives the field of single molecule enzymology. Here, we introduce recent progress in single enzyme molecule analysis in microwell arrays and discuss the challenges and opportunities. MDPI 2014-09-12 /pmc/articles/PMC6271441/ /pubmed/25221867 http://dx.doi.org/10.3390/molecules190914417 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Liebherr, Raphaela B.
Gorris, Hans H.
Enzyme Molecules in Solitary Confinement
title Enzyme Molecules in Solitary Confinement
title_full Enzyme Molecules in Solitary Confinement
title_fullStr Enzyme Molecules in Solitary Confinement
title_full_unstemmed Enzyme Molecules in Solitary Confinement
title_short Enzyme Molecules in Solitary Confinement
title_sort enzyme molecules in solitary confinement
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271441/
https://www.ncbi.nlm.nih.gov/pubmed/25221867
http://dx.doi.org/10.3390/molecules190914417
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