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...
Main Authors: | , |
---|---|
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 |
id |
doaj-976d931c2d424142bce8a47f2dd672e0 |
---|---|
record_format |
Article |
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 |
_version_ |
1724165793745207296 |