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Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function

Multidomain ATP-dependent Lon protease of E. coli (Ec-Lon) is one of the key enzymes of the quality control system of the cellular proteome. A recombinant form of Ec-Lon with deletion of the inserted characteristic α-helical HI(CC) domain (Lon-dHI(CC)) has been prepared and investigated to understan...

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Autores principales: Kudzhaev, A. M., Andrianova, A. G., Dubovtseva, E. S., Serova, O. V., Rotanova, T. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A.I. Gordeyev 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509003/
https://www.ncbi.nlm.nih.gov/pubmed/28740729
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author Kudzhaev, A. M.
Andrianova, A. G.
Dubovtseva, E. S.
Serova, O. V.
Rotanova, T. V.
author_facet Kudzhaev, A. M.
Andrianova, A. G.
Dubovtseva, E. S.
Serova, O. V.
Rotanova, T. V.
author_sort Kudzhaev, A. M.
collection PubMed
description Multidomain ATP-dependent Lon protease of E. coli (Ec-Lon) is one of the key enzymes of the quality control system of the cellular proteome. A recombinant form of Ec-Lon with deletion of the inserted characteristic α-helical HI(CC) domain (Lon-dHI(CC)) has been prepared and investigated to understand the role of this domain. A comparative study of the ATPase, proteolytic, and peptidase activities of the intact Lon protease and Lon-dHI(CC) has been carried out. The ability of the enzymes to undergo autolysis and their ability to bind DNA have been studied as well. It has been shown that the HI(CC) domain of Ec-Lon protease is required for the formation of a functionally active enzyme structure and for the implementation of protein-protein interactions.
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spelling pubmed-55090032017-07-24 Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function Kudzhaev, A. M. Andrianova, A. G. Dubovtseva, E. S. Serova, O. V. Rotanova, T. V. Acta Naturae Research Article Multidomain ATP-dependent Lon protease of E. coli (Ec-Lon) is one of the key enzymes of the quality control system of the cellular proteome. A recombinant form of Ec-Lon with deletion of the inserted characteristic α-helical HI(CC) domain (Lon-dHI(CC)) has been prepared and investigated to understand the role of this domain. A comparative study of the ATPase, proteolytic, and peptidase activities of the intact Lon protease and Lon-dHI(CC) has been carried out. The ability of the enzymes to undergo autolysis and their ability to bind DNA have been studied as well. It has been shown that the HI(CC) domain of Ec-Lon protease is required for the formation of a functionally active enzyme structure and for the implementation of protein-protein interactions. A.I. Gordeyev 2017 /pmc/articles/PMC5509003/ /pubmed/28740729 Text en Copyright ® 2017 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kudzhaev, A. M.
Andrianova, A. G.
Dubovtseva, E. S.
Serova, O. V.
Rotanova, T. V.
Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function
title Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function
title_full Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function
title_fullStr Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function
title_full_unstemmed Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function
title_short Role of the Inserted α-Helical Domain in E. coli ATP-Dependent Lon Protease Function
title_sort role of the inserted α-helical domain in e. coli atp-dependent lon protease function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509003/
https://www.ncbi.nlm.nih.gov/pubmed/28740729
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