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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
A.I. Gordeyev
2017
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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. |
format | Online Article Text |
id | pubmed-5509003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | A.I. Gordeyev |
record_format | MEDLINE/PubMed |
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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