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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Main Authors: Steven Shave, Nhan T. Pham, Connor B. Śmieja, Manfred Auer
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Methods and Protocols
Subjects:
Online Access:https://www.mdpi.com/2409-9279/3/3/55
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spelling 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
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