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Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells
Here we show that A-kinase anchoring protein 95 (AKAP95) and connexin 43 (Cx43) dynamically interact during cell cycle progression of lung cancer A549 cells. Interaction between AKAP95 and Cx43 at different cell cycle phases was examined by tandem mass spectrometry(MS/MS), confocal immunofluorescenc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754773/ https://www.ncbi.nlm.nih.gov/pubmed/26880274 http://dx.doi.org/10.1038/srep21224 |
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author | Chen, Xiaoxuan Kong, Xiangyu Zhuang, Wenxin Teng, Bogang Yu, Xiuyi Hua, Suhang Wang, Su Liang, Fengchao Ma, Dan Zhang, Suhui Zou, Xuan Dai, Yue Yang, Wei Zhang, Yongxing |
author_facet | Chen, Xiaoxuan Kong, Xiangyu Zhuang, Wenxin Teng, Bogang Yu, Xiuyi Hua, Suhang Wang, Su Liang, Fengchao Ma, Dan Zhang, Suhui Zou, Xuan Dai, Yue Yang, Wei Zhang, Yongxing |
author_sort | Chen, Xiaoxuan |
collection | PubMed |
description | Here we show that A-kinase anchoring protein 95 (AKAP95) and connexin 43 (Cx43) dynamically interact during cell cycle progression of lung cancer A549 cells. Interaction between AKAP95 and Cx43 at different cell cycle phases was examined by tandem mass spectrometry(MS/MS), confocal immunofluorescence microscopy, Western blot, and co-immunoprecipitation(Co-IP). Over the course of a complete cell cycle, interaction between AKAP95 and Cx43 occurred in two stages: binding stage from late G1 to metaphase, and separating stage from anaphase to late G1. The binding stage was further subdivided into complex binding to DNA in interphase and complex separating from DNA in metaphase. In late G1, Cx43 translocated to the nucleus via AKAP95; in anaphase, Cx43 separated from AKAP95 and aggregated between two daughter nuclei. In telophase, Cx43 aggregated at the membrane of the cleavage furrow. After mitosis, Cx43 was absent from the furrow membrane and was located in the cytoplasm. Binding between AKAP95 and Cx43 was reduced by N-(2-[P-Bromocinnamylamino]-ethyl)-5-isoquinolinesulfonmide (H89) treatment and enhanced by Forskolin. dynamic interaction between AKAP95 and Cx43 varies with cell cycle progression to regulate multiple biological processes. |
format | Online Article Text |
id | pubmed-4754773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47547732016-02-24 Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells Chen, Xiaoxuan Kong, Xiangyu Zhuang, Wenxin Teng, Bogang Yu, Xiuyi Hua, Suhang Wang, Su Liang, Fengchao Ma, Dan Zhang, Suhui Zou, Xuan Dai, Yue Yang, Wei Zhang, Yongxing Sci Rep Article Here we show that A-kinase anchoring protein 95 (AKAP95) and connexin 43 (Cx43) dynamically interact during cell cycle progression of lung cancer A549 cells. Interaction between AKAP95 and Cx43 at different cell cycle phases was examined by tandem mass spectrometry(MS/MS), confocal immunofluorescence microscopy, Western blot, and co-immunoprecipitation(Co-IP). Over the course of a complete cell cycle, interaction between AKAP95 and Cx43 occurred in two stages: binding stage from late G1 to metaphase, and separating stage from anaphase to late G1. The binding stage was further subdivided into complex binding to DNA in interphase and complex separating from DNA in metaphase. In late G1, Cx43 translocated to the nucleus via AKAP95; in anaphase, Cx43 separated from AKAP95 and aggregated between two daughter nuclei. In telophase, Cx43 aggregated at the membrane of the cleavage furrow. After mitosis, Cx43 was absent from the furrow membrane and was located in the cytoplasm. Binding between AKAP95 and Cx43 was reduced by N-(2-[P-Bromocinnamylamino]-ethyl)-5-isoquinolinesulfonmide (H89) treatment and enhanced by Forskolin. dynamic interaction between AKAP95 and Cx43 varies with cell cycle progression to regulate multiple biological processes. Nature Publishing Group 2016-02-16 /pmc/articles/PMC4754773/ /pubmed/26880274 http://dx.doi.org/10.1038/srep21224 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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 to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Chen, Xiaoxuan Kong, Xiangyu Zhuang, Wenxin Teng, Bogang Yu, Xiuyi Hua, Suhang Wang, Su Liang, Fengchao Ma, Dan Zhang, Suhui Zou, Xuan Dai, Yue Yang, Wei Zhang, Yongxing Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells |
title | Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells |
title_full | Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells |
title_fullStr | Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells |
title_full_unstemmed | Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells |
title_short | Dynamic changes in protein interaction between AKAP95 and Cx43 during cell cycle progression of A549 cells |
title_sort | dynamic changes in protein interaction between akap95 and cx43 during cell cycle progression of a549 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754773/ https://www.ncbi.nlm.nih.gov/pubmed/26880274 http://dx.doi.org/10.1038/srep21224 |
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