Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties
Quantitative microdialysis is a traditional biophysical affinity determination technique. In the development of the detailed experimental protocol presented, we used commercially available equipment, rapid equilibrium dialysis (RED) devices (ThermoFisher Scientific), which means that it is open to m...
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doaj-584297e7854f49fb8c08ddd461ed5cf22020-11-25T02:55:52ZengMDPI AGMethods and Protocols2409-92792020-07-013555510.3390/mps3030055Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical PropertiesSteven Shave0Nhan T. Pham1Connor B. Śmieja2Manfred Auer3School of Biological Sciences, IQB3, University of Edinburgh, The King’s Buildings, Max Born Crescent, CH Waddington Building, Edinburgh, Scotland EH9 3BF, UKSchool of Biological Sciences, IQB3, University of Edinburgh, The King’s Buildings, Max Born Crescent, CH Waddington Building, Edinburgh, Scotland EH9 3BF, UKSchool of Biological Sciences, IQB3, University of Edinburgh, The King’s Buildings, Max Born Crescent, CH Waddington Building, Edinburgh, Scotland EH9 3BF, UKSchool of Biological Sciences, IQB3, University of Edinburgh, The King’s Buildings, Max Born Crescent, CH Waddington Building, Edinburgh, Scotland EH9 3BF, UKQuantitative microdialysis is a traditional biophysical affinity determination technique. In the development of the detailed experimental protocol presented, we used commercially available equipment, rapid equilibrium dialysis (RED) devices (ThermoFisher Scientific), which means that it is open to most laboratories. The target protein and test compound are incubated in a chamber partitioned to allow only small molecules to transition to a larger reservoir chamber, then reversed-phase high performance liquid chromatography (RP-HPLC) or liquid chromatography–mass spectrometry (LC–MS) is used to determine the abundance of compound in each chamber. A higher compound concentration measured in the chamber that contains the target protein indicates binding. As a novel, and differentiating contribution, we present a protocol for mathematical analysis of experimental data. We provide the equations and the software to yield dissociation constants for the test compound-target protein complex up to 0.5 mM K<sub>D</sub>, and we quantitatively discuss the limitations of affinities in relation to measured compound concentrations.https://www.mdpi.com/2409-9279/3/3/55label free screeningaffinity determinationdialysisK<sub>D</sub> determinationpromiscuityaggregation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Steven Shave Nhan T. Pham Connor B. Śmieja Manfred Auer |
spellingShingle |
Steven Shave Nhan T. Pham Connor B. Śmieja Manfred Auer Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties Methods and Protocols label free screening affinity determination dialysis K<sub>D</sub> determination promiscuity aggregation |
author_facet |
Steven Shave Nhan T. Pham Connor B. Śmieja Manfred Auer |
author_sort |
Steven Shave |
title |
Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties |
title_short |
Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties |
title_full |
Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties |
title_fullStr |
Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties |
title_full_unstemmed |
Quantitative Microdialysis: Experimental Protocol and Software for Small Molecule Protein Affinity Determination and for Exclusion of Compounds with Poor Physicochemical Properties |
title_sort |
quantitative microdialysis: experimental protocol and software for small molecule protein affinity determination and for exclusion of compounds with poor physicochemical properties |
publisher |
MDPI AG |
series |
Methods and Protocols |
issn |
2409-9279 |
publishDate |
2020-07-01 |
description |
Quantitative microdialysis is a traditional biophysical affinity determination technique. In the development of the detailed experimental protocol presented, we used commercially available equipment, rapid equilibrium dialysis (RED) devices (ThermoFisher Scientific), which means that it is open to most laboratories. The target protein and test compound are incubated in a chamber partitioned to allow only small molecules to transition to a larger reservoir chamber, then reversed-phase high performance liquid chromatography (RP-HPLC) or liquid chromatography–mass spectrometry (LC–MS) is used to determine the abundance of compound in each chamber. A higher compound concentration measured in the chamber that contains the target protein indicates binding. As a novel, and differentiating contribution, we present a protocol for mathematical analysis of experimental data. We provide the equations and the software to yield dissociation constants for the test compound-target protein complex up to 0.5 mM K<sub>D</sub>, and we quantitatively discuss the limitations of affinities in relation to measured compound concentrations. |
topic |
label free screening affinity determination dialysis K<sub>D</sub> determination promiscuity aggregation |
url |
https://www.mdpi.com/2409-9279/3/3/55 |
work_keys_str_mv |
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