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Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners
CK2β is the non‐catalytic modulating part of the S/T‐protein kinase CK2. However, the overall function of CK2β is poorly understood. Here, we report on the identification of 38 new interaction partners of the human CK2β from lysates of DU145 prostate cancer cells using photo‐crosslinking and mass sp...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983076/ https://www.ncbi.nlm.nih.gov/pubmed/36876296 http://dx.doi.org/10.1096/fba.2022-00098 |
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author | Nickelsen, Anna Götz, Claudia Lenz, Florian Niefind, Karsten König, Simone Jose, Joachim |
author_facet | Nickelsen, Anna Götz, Claudia Lenz, Florian Niefind, Karsten König, Simone Jose, Joachim |
author_sort | Nickelsen, Anna |
collection | PubMed |
description | CK2β is the non‐catalytic modulating part of the S/T‐protein kinase CK2. However, the overall function of CK2β is poorly understood. Here, we report on the identification of 38 new interaction partners of the human CK2β from lysates of DU145 prostate cancer cells using photo‐crosslinking and mass spectrometry, whereby HSP70‐1 was identified with high abundance. The K(D) value of its interaction with CK2β was determined as 0.57 μM by microscale thermophoresis, this being the first time, to our knowledge, that a K(D) value of CK2β with another protein than CK2α or CK2α′ was quantified. Phosphorylation studies excluded HSP70‐1 as a substrate or activity modulator of CK2, suggesting a CK2 activity independent interaction of HSP70‐1 with CK2β. Co‐immunoprecipitation experiments in three different cancer cell lines confirmed the interaction of HSP70‐1 with CK2β in vivo. A second identified CK2β interaction partner was Rho guanin nucleotide exchange factor 12, indicating an involvement of CK2β in the Rho‐GTPase signal pathway, described here for the first time to our knowledge. This points to a role of CK2β in the interaction network affecting the organization of the cytoskeleton. |
format | Online Article Text |
id | pubmed-9983076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99830762023-03-04 Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners Nickelsen, Anna Götz, Claudia Lenz, Florian Niefind, Karsten König, Simone Jose, Joachim FASEB Bioadv Research Articles CK2β is the non‐catalytic modulating part of the S/T‐protein kinase CK2. However, the overall function of CK2β is poorly understood. Here, we report on the identification of 38 new interaction partners of the human CK2β from lysates of DU145 prostate cancer cells using photo‐crosslinking and mass spectrometry, whereby HSP70‐1 was identified with high abundance. The K(D) value of its interaction with CK2β was determined as 0.57 μM by microscale thermophoresis, this being the first time, to our knowledge, that a K(D) value of CK2β with another protein than CK2α or CK2α′ was quantified. Phosphorylation studies excluded HSP70‐1 as a substrate or activity modulator of CK2, suggesting a CK2 activity independent interaction of HSP70‐1 with CK2β. Co‐immunoprecipitation experiments in three different cancer cell lines confirmed the interaction of HSP70‐1 with CK2β in vivo. A second identified CK2β interaction partner was Rho guanin nucleotide exchange factor 12, indicating an involvement of CK2β in the Rho‐GTPase signal pathway, described here for the first time to our knowledge. This points to a role of CK2β in the interaction network affecting the organization of the cytoskeleton. John Wiley and Sons Inc. 2023-01-22 /pmc/articles/PMC9983076/ /pubmed/36876296 http://dx.doi.org/10.1096/fba.2022-00098 Text en © 2023 The Authors. FASEB BioAdvances published by Wiley Periodicals LLC on behalf of The Federation of American Societies for Experimental Biology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Nickelsen, Anna Götz, Claudia Lenz, Florian Niefind, Karsten König, Simone Jose, Joachim Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners |
title | Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners |
title_full | Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners |
title_fullStr | Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners |
title_full_unstemmed | Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners |
title_short | Analyzing the interactome of human CK2β in prostate carcinoma cells reveals HSP70‐1 and Rho guanin nucleotide exchange factor 12 as novel interaction partners |
title_sort | analyzing the interactome of human ck2β in prostate carcinoma cells reveals hsp70‐1 and rho guanin nucleotide exchange factor 12 as novel interaction partners |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983076/ https://www.ncbi.nlm.nih.gov/pubmed/36876296 http://dx.doi.org/10.1096/fba.2022-00098 |
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