Enzyme Molecules in Solitary Confinement

被引:17
|
作者
Liebherr, Raphaela B. [1 ]
Gorris, Hans H. [1 ]
机构
[1] Univ Regensburg, Inst Analyt Chem Chemo & Biosensors, D-93040 Regensburg, Germany
来源
MOLECULES | 2014年 / 19卷 / 09期
关键词
enzyme kinetics; single molecule enzymology; fluorescence microscopy; femtoliter array; COLI BETA-GALACTOSIDASE; BACTERIAL-CELL ARRAY; SINGLE-MOLECULE; INDIVIDUAL MOLECULES; FLUORESCENCE SPECTROSCOPY; ALKALINE-PHOSPHATASE; ELECTROPHORETIC HETEROGENEITY; MICROFABRICATED ARRAYS; THERMAL-DENATURATION; DYNAMIC DISORDER;
D O I
10.3390/molecules190914417
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:14417 / 14445
页数:29
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