Cargando…
Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II
The calcium calmodulin-dependent protein kinase II (CaMKII) is a dodecameric holoenzyme important for encoding memory. Its activation, triggered by binding of calcium-calmodulin, persists autonomously after calmodulin dissociation. One (receiver) kinase captures and subsequently phosphorylates the r...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6576796/ https://www.ncbi.nlm.nih.gov/pubmed/31150387 http://dx.doi.org/10.1371/journal.pcbi.1006796 |
_version_ | 1783427844708237312 |
---|---|
author | Pandini, Alessandro Schulman, Howard Khan, Shahid |
author_facet | Pandini, Alessandro Schulman, Howard Khan, Shahid |
author_sort | Pandini, Alessandro |
collection | PubMed |
description | The calcium calmodulin-dependent protein kinase II (CaMKII) is a dodecameric holoenzyme important for encoding memory. Its activation, triggered by binding of calcium-calmodulin, persists autonomously after calmodulin dissociation. One (receiver) kinase captures and subsequently phosphorylates the regulatory domain peptide of a donor kinase forming a chained dimer as the first stage of autonomous activation. Protein dynamics simulations examined the conformational changes triggered by dimer formation and phosphorylation, aimed to provide a molecular rationale for human mutations that result in learning disabilities. Ensembles generated from X-ray crystal structures were characterized by network centrality and community analysis. Mutual information related collective motions to local fragment dynamics encoded with a structural alphabet. Implicit solvent tCONCOORD conformational ensembles revealed the dynamic architecture of inactive kinase domains was co-opted in the activated dimer but the network hub shifted from the nucleotide binding cleft to the captured peptide. Explicit solvent molecular dynamics (MD) showed nucleotide and substrate binding determinants formed coupled nodes in long-range signal relays between regulatory peptides in the dimer. Strain in the extended captured peptide was balanced by reduced flexibility of the receiver kinase C-lobe core. The relays were organized around a hydrophobic patch between the captured peptide and a key binding helix. The human mutations aligned along the relays. Thus, these mutations could disrupt the allosteric network alternatively, or in addition, to altered binding affinities. Non-binding protein sectors distant from the binding sites mediated the allosteric signalling; providing possible targets for inhibitor design. Phosphorylation of the peptide modulated the dielectric of its binding pocket to strengthen the patch, non-binding sectors, domain interface and temporal correlations between parallel relays. These results provide the molecular details underlying the reported positive kinase cooperativity to enrich the discussion on how autonomous activation by phosphorylation leads to long-term behavioural effects. |
format | Online Article Text |
id | pubmed-6576796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65767962019-06-28 Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II Pandini, Alessandro Schulman, Howard Khan, Shahid PLoS Comput Biol Research Article The calcium calmodulin-dependent protein kinase II (CaMKII) is a dodecameric holoenzyme important for encoding memory. Its activation, triggered by binding of calcium-calmodulin, persists autonomously after calmodulin dissociation. One (receiver) kinase captures and subsequently phosphorylates the regulatory domain peptide of a donor kinase forming a chained dimer as the first stage of autonomous activation. Protein dynamics simulations examined the conformational changes triggered by dimer formation and phosphorylation, aimed to provide a molecular rationale for human mutations that result in learning disabilities. Ensembles generated from X-ray crystal structures were characterized by network centrality and community analysis. Mutual information related collective motions to local fragment dynamics encoded with a structural alphabet. Implicit solvent tCONCOORD conformational ensembles revealed the dynamic architecture of inactive kinase domains was co-opted in the activated dimer but the network hub shifted from the nucleotide binding cleft to the captured peptide. Explicit solvent molecular dynamics (MD) showed nucleotide and substrate binding determinants formed coupled nodes in long-range signal relays between regulatory peptides in the dimer. Strain in the extended captured peptide was balanced by reduced flexibility of the receiver kinase C-lobe core. The relays were organized around a hydrophobic patch between the captured peptide and a key binding helix. The human mutations aligned along the relays. Thus, these mutations could disrupt the allosteric network alternatively, or in addition, to altered binding affinities. Non-binding protein sectors distant from the binding sites mediated the allosteric signalling; providing possible targets for inhibitor design. Phosphorylation of the peptide modulated the dielectric of its binding pocket to strengthen the patch, non-binding sectors, domain interface and temporal correlations between parallel relays. These results provide the molecular details underlying the reported positive kinase cooperativity to enrich the discussion on how autonomous activation by phosphorylation leads to long-term behavioural effects. Public Library of Science 2019-05-31 /pmc/articles/PMC6576796/ /pubmed/31150387 http://dx.doi.org/10.1371/journal.pcbi.1006796 Text en © 2019 Pandini et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Pandini, Alessandro Schulman, Howard Khan, Shahid Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II |
title | Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II |
title_full | Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II |
title_fullStr | Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II |
title_full_unstemmed | Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II |
title_short | Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II |
title_sort | conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase ii |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6576796/ https://www.ncbi.nlm.nih.gov/pubmed/31150387 http://dx.doi.org/10.1371/journal.pcbi.1006796 |
work_keys_str_mv | AT pandinialessandro conformationalcouplingbytransphosphorylationincalciumcalmodulindependentkinaseii AT schulmanhoward conformationalcouplingbytransphosphorylationincalciumcalmodulindependentkinaseii AT khanshahid conformationalcouplingbytransphosphorylationincalciumcalmodulindependentkinaseii |