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GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers
Peptide pore blockers and their fluorescent derivatives are useful molecular probes to study the structure and functions of the voltage-gated potassium Kv1.3 channel, which is considered as a pharmacological target in the treatment of autoimmune and neurological disorders. We present Kv1.3 fluoresce...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835862/ https://www.ncbi.nlm.nih.gov/pubmed/35163644 http://dx.doi.org/10.3390/ijms23031724 |
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author | Denisova, Kristina R. Orlov, Nikita A. Yakimov, Sergey A. Kryukova, Elena A. Dolgikh, Dmitry A. Kirpichnikov, Mikhail P. Feofanov, Alexey V. Nekrasova, Oksana V. |
author_facet | Denisova, Kristina R. Orlov, Nikita A. Yakimov, Sergey A. Kryukova, Elena A. Dolgikh, Dmitry A. Kirpichnikov, Mikhail P. Feofanov, Alexey V. Nekrasova, Oksana V. |
author_sort | Denisova, Kristina R. |
collection | PubMed |
description | Peptide pore blockers and their fluorescent derivatives are useful molecular probes to study the structure and functions of the voltage-gated potassium Kv1.3 channel, which is considered as a pharmacological target in the treatment of autoimmune and neurological disorders. We present Kv1.3 fluorescent ligand, GFP–MgTx, constructed on the basis of green fluorescent protein (GFP) and margatoxin (MgTx), the peptide, which is widely used in physiological studies of Kv1.3. Expression of the fluorescent ligand in E. coli cells resulted in correctly folded and functionally active GFP–MgTx with a yield of 30 mg per 1 L of culture. Complex of GFP–MgTx with the Kv1.3 binding site is reported to have the dissociation constant of 11 ± 2 nM. GFP–MgTx as a component of an analytical system based on the hybrid KcsA–Kv1.3 channel is shown to be applicable to recognize Kv1.3 pore blockers of peptide origin and to evaluate their affinities to Kv1.3. GFP–MgTx can be used in screening and pre-selection of Kv1.3 channel blockers as potential drug candidates. |
format | Online Article Text |
id | pubmed-8835862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88358622022-02-12 GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers Denisova, Kristina R. Orlov, Nikita A. Yakimov, Sergey A. Kryukova, Elena A. Dolgikh, Dmitry A. Kirpichnikov, Mikhail P. Feofanov, Alexey V. Nekrasova, Oksana V. Int J Mol Sci Article Peptide pore blockers and their fluorescent derivatives are useful molecular probes to study the structure and functions of the voltage-gated potassium Kv1.3 channel, which is considered as a pharmacological target in the treatment of autoimmune and neurological disorders. We present Kv1.3 fluorescent ligand, GFP–MgTx, constructed on the basis of green fluorescent protein (GFP) and margatoxin (MgTx), the peptide, which is widely used in physiological studies of Kv1.3. Expression of the fluorescent ligand in E. coli cells resulted in correctly folded and functionally active GFP–MgTx with a yield of 30 mg per 1 L of culture. Complex of GFP–MgTx with the Kv1.3 binding site is reported to have the dissociation constant of 11 ± 2 nM. GFP–MgTx as a component of an analytical system based on the hybrid KcsA–Kv1.3 channel is shown to be applicable to recognize Kv1.3 pore blockers of peptide origin and to evaluate their affinities to Kv1.3. GFP–MgTx can be used in screening and pre-selection of Kv1.3 channel blockers as potential drug candidates. MDPI 2022-02-02 /pmc/articles/PMC8835862/ /pubmed/35163644 http://dx.doi.org/10.3390/ijms23031724 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Denisova, Kristina R. Orlov, Nikita A. Yakimov, Sergey A. Kryukova, Elena A. Dolgikh, Dmitry A. Kirpichnikov, Mikhail P. Feofanov, Alexey V. Nekrasova, Oksana V. GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers |
title | GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers |
title_full | GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers |
title_fullStr | GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers |
title_full_unstemmed | GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers |
title_short | GFP–Margatoxin, a Genetically Encoded Fluorescent Ligand to Probe Affinity of Kv1.3 Channel Blockers |
title_sort | gfp–margatoxin, a genetically encoded fluorescent ligand to probe affinity of kv1.3 channel blockers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835862/ https://www.ncbi.nlm.nih.gov/pubmed/35163644 http://dx.doi.org/10.3390/ijms23031724 |
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