Cargando…
Efficient and cost effective production of active-form human PKB using silkworm larvae
Protein kinase B (PKB) also known as Akt is involved in many signal transduction pathways. As alterations of the PKB pathway are found in a number of human malignancies, PKB is considered an important drug target for cancer therapy. However, production of sufficient amounts of active PKB for biochem...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133716/ https://www.ncbi.nlm.nih.gov/pubmed/25125290 http://dx.doi.org/10.1038/srep06016 |
_version_ | 1782330778991984640 |
---|---|
author | Maesaki, Ryoko Satoh, Ryosuke Taoka, Masato Kanaba, Teppei Asano, Tsunaki Fujita, Chiharu Fujiwara, Toshinobu Ito, Yutaka Isobe, Toshiaki Hakoshima, Toshio Maenaka, Katsumi Mishima, Masaki |
author_facet | Maesaki, Ryoko Satoh, Ryosuke Taoka, Masato Kanaba, Teppei Asano, Tsunaki Fujita, Chiharu Fujiwara, Toshinobu Ito, Yutaka Isobe, Toshiaki Hakoshima, Toshio Maenaka, Katsumi Mishima, Masaki |
author_sort | Maesaki, Ryoko |
collection | PubMed |
description | Protein kinase B (PKB) also known as Akt is involved in many signal transduction pathways. As alterations of the PKB pathway are found in a number of human malignancies, PKB is considered an important drug target for cancer therapy. However, production of sufficient amounts of active PKB for biochemical and structural studies is very costly because of the necessity of using a higher organism expression system to obtain phosphorylated PKB. Here, we report efficient production of active PKBα using the BmNPV bacmid expression system with silkworm larvae. Following direct injection of bacmid DNA, recombinant PKBα protein was highly expressed in the fat bodies of larvae, and could be purified using a GST-tag and then cleaved. A final yield of approximately 1 mg PKBα/20 larvae was recorded. Kinase assays showed that the recombinant PKBα possessed high phosphorylation activity. We further confirmed phosphorylation on the activation loop by mass spectrometric analysis. Our results indicate that the silkworm expression system is of value for preparation of active-form PKBα with phosphorylation on the activation loop. This efficient production of the active protein will facilitate further biochemical and structural studies and stimulate subsequent drug development. |
format | Online Article Text |
id | pubmed-4133716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41337162014-08-18 Efficient and cost effective production of active-form human PKB using silkworm larvae Maesaki, Ryoko Satoh, Ryosuke Taoka, Masato Kanaba, Teppei Asano, Tsunaki Fujita, Chiharu Fujiwara, Toshinobu Ito, Yutaka Isobe, Toshiaki Hakoshima, Toshio Maenaka, Katsumi Mishima, Masaki Sci Rep Article Protein kinase B (PKB) also known as Akt is involved in many signal transduction pathways. As alterations of the PKB pathway are found in a number of human malignancies, PKB is considered an important drug target for cancer therapy. However, production of sufficient amounts of active PKB for biochemical and structural studies is very costly because of the necessity of using a higher organism expression system to obtain phosphorylated PKB. Here, we report efficient production of active PKBα using the BmNPV bacmid expression system with silkworm larvae. Following direct injection of bacmid DNA, recombinant PKBα protein was highly expressed in the fat bodies of larvae, and could be purified using a GST-tag and then cleaved. A final yield of approximately 1 mg PKBα/20 larvae was recorded. Kinase assays showed that the recombinant PKBα possessed high phosphorylation activity. We further confirmed phosphorylation on the activation loop by mass spectrometric analysis. Our results indicate that the silkworm expression system is of value for preparation of active-form PKBα with phosphorylation on the activation loop. This efficient production of the active protein will facilitate further biochemical and structural studies and stimulate subsequent drug development. Nature Publishing Group 2014-08-15 /pmc/articles/PMC4133716/ /pubmed/25125290 http://dx.doi.org/10.1038/srep06016 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Article Maesaki, Ryoko Satoh, Ryosuke Taoka, Masato Kanaba, Teppei Asano, Tsunaki Fujita, Chiharu Fujiwara, Toshinobu Ito, Yutaka Isobe, Toshiaki Hakoshima, Toshio Maenaka, Katsumi Mishima, Masaki Efficient and cost effective production of active-form human PKB using silkworm larvae |
title | Efficient and cost effective production of active-form human PKB using silkworm larvae |
title_full | Efficient and cost effective production of active-form human PKB using silkworm larvae |
title_fullStr | Efficient and cost effective production of active-form human PKB using silkworm larvae |
title_full_unstemmed | Efficient and cost effective production of active-form human PKB using silkworm larvae |
title_short | Efficient and cost effective production of active-form human PKB using silkworm larvae |
title_sort | efficient and cost effective production of active-form human pkb using silkworm larvae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133716/ https://www.ncbi.nlm.nih.gov/pubmed/25125290 http://dx.doi.org/10.1038/srep06016 |
work_keys_str_mv | AT maesakiryoko efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT satohryosuke efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT taokamasato efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT kanabateppei efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT asanotsunaki efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT fujitachiharu efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT fujiwaratoshinobu efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT itoyutaka efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT isobetoshiaki efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT hakoshimatoshio efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT maenakakatsumi efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae AT mishimamasaki efficientandcosteffectiveproductionofactiveformhumanpkbusingsilkwormlarvae |