Cargando…

The structural basis of the multi-step allosteric activation of Aurora B kinase

Aurora B, together with IN-box, the C-terminal part of INCENP, forms an enzymatic complex that ensures faithful cell division. The [Aurora B/IN-box] complex is activated by autophosphorylation in the Aurora B activation loop and in IN-box, but it is not clear how these phosphorylations activate the...

Descripción completa

Detalles Bibliográficos
Autores principales: Segura-Peña, Dario, Hovet, Oda, Gogoi, Hemanga, Dawicki-McKenna, Jennine, Hansen Wøien, Stine Malene, Carrer, Manuel, Black, Ben E, Cascella, Michele, Sekulic, Nikolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259393/
https://www.ncbi.nlm.nih.gov/pubmed/37227118
http://dx.doi.org/10.7554/eLife.85328
_version_ 1785057651803029504
author Segura-Peña, Dario
Hovet, Oda
Gogoi, Hemanga
Dawicki-McKenna, Jennine
Hansen Wøien, Stine Malene
Carrer, Manuel
Black, Ben E
Cascella, Michele
Sekulic, Nikolina
author_facet Segura-Peña, Dario
Hovet, Oda
Gogoi, Hemanga
Dawicki-McKenna, Jennine
Hansen Wøien, Stine Malene
Carrer, Manuel
Black, Ben E
Cascella, Michele
Sekulic, Nikolina
author_sort Segura-Peña, Dario
collection PubMed
description Aurora B, together with IN-box, the C-terminal part of INCENP, forms an enzymatic complex that ensures faithful cell division. The [Aurora B/IN-box] complex is activated by autophosphorylation in the Aurora B activation loop and in IN-box, but it is not clear how these phosphorylations activate the enzyme. We used a combination of experimental and computational studies to investigate the effects of phosphorylation on the molecular dynamics and structure of [Aurora B/IN-box]. In addition, we generated partially phosphorylated intermediates to analyze the contribution of each phosphorylation independently. We found that the dynamics of Aurora and IN-box are interconnected, and IN-box plays both positive and negative regulatory roles depending on the phosphorylation status of the enzyme complex. Phosphorylation in the activation loop of Aurora B occurs intramolecularly and prepares the enzyme complex for activation, but two phosphorylated sites are synergistically responsible for full enzyme activity.
format Online
Article
Text
id pubmed-10259393
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-102593932023-06-13 The structural basis of the multi-step allosteric activation of Aurora B kinase Segura-Peña, Dario Hovet, Oda Gogoi, Hemanga Dawicki-McKenna, Jennine Hansen Wøien, Stine Malene Carrer, Manuel Black, Ben E Cascella, Michele Sekulic, Nikolina eLife Biochemistry and Chemical Biology Aurora B, together with IN-box, the C-terminal part of INCENP, forms an enzymatic complex that ensures faithful cell division. The [Aurora B/IN-box] complex is activated by autophosphorylation in the Aurora B activation loop and in IN-box, but it is not clear how these phosphorylations activate the enzyme. We used a combination of experimental and computational studies to investigate the effects of phosphorylation on the molecular dynamics and structure of [Aurora B/IN-box]. In addition, we generated partially phosphorylated intermediates to analyze the contribution of each phosphorylation independently. We found that the dynamics of Aurora and IN-box are interconnected, and IN-box plays both positive and negative regulatory roles depending on the phosphorylation status of the enzyme complex. Phosphorylation in the activation loop of Aurora B occurs intramolecularly and prepares the enzyme complex for activation, but two phosphorylated sites are synergistically responsible for full enzyme activity. eLife Sciences Publications, Ltd 2023-05-25 /pmc/articles/PMC10259393/ /pubmed/37227118 http://dx.doi.org/10.7554/eLife.85328 Text en © 2023, Segura-Peña et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry and Chemical Biology
Segura-Peña, Dario
Hovet, Oda
Gogoi, Hemanga
Dawicki-McKenna, Jennine
Hansen Wøien, Stine Malene
Carrer, Manuel
Black, Ben E
Cascella, Michele
Sekulic, Nikolina
The structural basis of the multi-step allosteric activation of Aurora B kinase
title The structural basis of the multi-step allosteric activation of Aurora B kinase
title_full The structural basis of the multi-step allosteric activation of Aurora B kinase
title_fullStr The structural basis of the multi-step allosteric activation of Aurora B kinase
title_full_unstemmed The structural basis of the multi-step allosteric activation of Aurora B kinase
title_short The structural basis of the multi-step allosteric activation of Aurora B kinase
title_sort structural basis of the multi-step allosteric activation of aurora b kinase
topic Biochemistry and Chemical Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259393/
https://www.ncbi.nlm.nih.gov/pubmed/37227118
http://dx.doi.org/10.7554/eLife.85328
work_keys_str_mv AT segurapenadario thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT hovetoda thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT gogoihemanga thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT dawickimckennajennine thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT hansenwøienstinemalene thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT carrermanuel thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT blackbene thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT cascellamichele thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT sekulicnikolina thestructuralbasisofthemultistepallostericactivationofaurorabkinase
AT segurapenadario structuralbasisofthemultistepallostericactivationofaurorabkinase
AT hovetoda structuralbasisofthemultistepallostericactivationofaurorabkinase
AT gogoihemanga structuralbasisofthemultistepallostericactivationofaurorabkinase
AT dawickimckennajennine structuralbasisofthemultistepallostericactivationofaurorabkinase
AT hansenwøienstinemalene structuralbasisofthemultistepallostericactivationofaurorabkinase
AT carrermanuel structuralbasisofthemultistepallostericactivationofaurorabkinase
AT blackbene structuralbasisofthemultistepallostericactivationofaurorabkinase
AT cascellamichele structuralbasisofthemultistepallostericactivationofaurorabkinase
AT sekulicnikolina structuralbasisofthemultistepallostericactivationofaurorabkinase