A quantitative continuous enzyme assay of intramolecularly quenched fluorogenic phospholipase substrates for molecular imaging

被引:8
|
作者
Mawn, Theresa M. [1 ]
Popov, Anatoliy V. [1 ]
Delikatny, E. James [1 ]
机构
[1] Univ Penn, Mol Imaging Lab, Dept Radiol, Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
Surface dilution enzyme kinetics; Fluorescence assay; Phosphatidylcholine-specific phospholipase C; Aggregation; Self-quenching molecular imaging agents; INTERFACIAL CATALYSIS; PHOTODYNAMIC THERAPY; BACILLUS-CEREUS; MIXED MICELLES; PHOSPHATIDYLCHOLINE; ACTIVATION; KINETICS; SPECIFICITY; PHASE; RAS;
D O I
10.1016/j.ab.2011.12.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
There has been recent growth in the development of activatable near-infrared (NIR) fluorescent probes for molecular imaging, generally designed by placing fluorochromes on a cleavable substrate in close proximity to one another, such that they self-quench, but fluoresce on separation via enzymatic cleavage of the substrate. Although these probes offer excellent contrast, the detection of enzyme activity has largely only been described qualitatively. In order to assess the effectiveness of a probe, it is useful to have a quantitative measure, such as the enzyme-substrate kinetic parameters. We have developed an assay to determine kinetic parameters and applied it to an intramolecularly quenched molecule, Pyro-PtdEtn-BHQ a NIR fluorescent probe specific to phosphatidylcholine-specific phospholipase C. The development of this assay includes corrections for intermolecular quenching, calibration, optimization of reaction mixtures, and determination of kinetic and inhibition parameters. This assay can easily be extended to analyze and compare the efficiency of other fluorescent activatable phospholipase probes as suitable molecular imaging agents. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:96 / 102
页数:7
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