Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli

Cytosolic carboxypeptidase 6 (CCP6) is a member of cytosolic carboxypeptidase (CCP) family that catalyze the removal of polyglutamate side chains from protein substrates. Biochemical and biophysical characterization of CCPs requires large quantities of purified proteins. However, no method describin...

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Main Authors: Wang Ruixue, Wu Hui-Yuan
Format: Article
Language:English
Published: EDP Sciences 2020-01-01
Series:E3S Web of Conferences
Online Access:https://www.e3s-conferences.org/articles/e3sconf/pdf/2020/45/e3sconf_iceeb2020_04050.pdf
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spelling doaj-976d931c2d424142bce8a47f2dd672e02021-04-02T11:03:49ZengEDP SciencesE3S Web of Conferences2267-12422020-01-011850405010.1051/e3sconf/202018504050e3sconf_iceeb2020_04050Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coliWang Ruixue0Wu Hui-Yuan1School of Pharmaceutical Science and Technology, Tianjin UniversitySchool of Pharmaceutical Science and Technology, Tianjin UniversityCytosolic carboxypeptidase 6 (CCP6) is a member of cytosolic carboxypeptidase (CCP) family that catalyze the removal of polyglutamate side chains from protein substrates. Biochemical and biophysical characterization of CCPs requires large quantities of purified proteins. However, no method describing the expression of any mammalian CCP family member from bacteria has been published to our best knowledge. After considerable efforts to improve the solubility of mammalian CCPs expressed in bacteria, including the optimization of induction temperature and by using different receptive cells, we were able to get less expression of mouse CCP6 in soluble fraction of bacterial lysates. We report in this article, the bacterial expression of CCP6 using Arctic Express (DE3) competent cells that co-express the chaperonin system GroEL and GroES from Oleispira antarctica. However, to achieve a large number of soluble target proteins, the expression conditions still need to be further optimized.https://www.e3s-conferences.org/articles/e3sconf/pdf/2020/45/e3sconf_iceeb2020_04050.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Wang Ruixue
Wu Hui-Yuan
spellingShingle Wang Ruixue
Wu Hui-Yuan
Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli
E3S Web of Conferences
author_facet Wang Ruixue
Wu Hui-Yuan
author_sort Wang Ruixue
title Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli
title_short Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli
title_full Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli
title_fullStr Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli
title_full_unstemmed Expression of recombinant mouse cytosolic carboxypeptidase 6 in Escherichia coli
title_sort expression of recombinant mouse cytosolic carboxypeptidase 6 in escherichia coli
publisher EDP Sciences
series E3S Web of Conferences
issn 2267-1242
publishDate 2020-01-01
description Cytosolic carboxypeptidase 6 (CCP6) is a member of cytosolic carboxypeptidase (CCP) family that catalyze the removal of polyglutamate side chains from protein substrates. Biochemical and biophysical characterization of CCPs requires large quantities of purified proteins. However, no method describing the expression of any mammalian CCP family member from bacteria has been published to our best knowledge. After considerable efforts to improve the solubility of mammalian CCPs expressed in bacteria, including the optimization of induction temperature and by using different receptive cells, we were able to get less expression of mouse CCP6 in soluble fraction of bacterial lysates. We report in this article, the bacterial expression of CCP6 using Arctic Express (DE3) competent cells that co-express the chaperonin system GroEL and GroES from Oleispira antarctica. However, to achieve a large number of soluble target proteins, the expression conditions still need to be further optimized.
url https://www.e3s-conferences.org/articles/e3sconf/pdf/2020/45/e3sconf_iceeb2020_04050.pdf
work_keys_str_mv AT wangruixue expressionofrecombinantmousecytosoliccarboxypeptidase6inescherichiacoli
AT wuhuiyuan expressionofrecombinantmousecytosoliccarboxypeptidase6inescherichiacoli
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