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Liebherr, Raphaela ; Gorris, H. H.

Enzyme Molecules in Solitary Confinement

Liebherr, Raphaela and Gorris, H. H. (2014) Enzyme Molecules in Solitary Confinement. Molecules 19, pp. 1417-1445.

Date of publication of this fulltext: 04 Feb 2015 14:59
Article
DOI to cite this document: 10.5283/epub.31285


Abstract

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 ...

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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Details

Item typeArticle
Journal or Publication TitleMolecules
Publisher:MDPI
Volume:19
Page Range:pp. 1417-1445
Date2014
InstitutionsChemistry and Pharmacy > Institut für Analytische Chemie, Chemo- und Biosensorik > Bioanalytik und Biosensorik (Prof. Joachim Wegener)
Identification Number
ValueType
10.3390/molecules190914417DOI
Keywordsenzyme kinetics; single molecule enzymology; fluorescence microscopy; femtoliter array
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-312858
Item ID31285

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