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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...

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Autores principales: Maesaki, Ryoko, Satoh, Ryosuke, Taoka, Masato, Kanaba, Teppei, Asano, Tsunaki, Fujita, Chiharu, Fujiwara, Toshinobu, Ito, Yutaka, Isobe, Toshiaki, Hakoshima, Toshio, Maenaka, Katsumi, Mishima, Masaki
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
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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.
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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
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