Self-Assembly of a Designed Nucleoprotein Architecture through Multimodal Interactions.

Détails

ID Serval
serval:BIB_7E7BA844B296
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Self-Assembly of a Designed Nucleoprotein Architecture through Multimodal Interactions.
Périodique
ACS central science
Auteur⸱e⸱s
Subramanian R.H., Smith S.J., Alberstein R.G., Bailey J.B., Zhang L., Cardone G., Suominen L., Chami M., Stahlberg H., Baker T.S., Tezcan F.A.
ISSN
2374-7943 (Print)
ISSN-L
2374-7943
Statut éditorial
Publié
Date de publication
28/11/2018
Peer-reviewed
Oui
Volume
4
Numéro
11
Pages
1578-1586
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
The co-self-assembly of proteins and nucleic acids (NAs) produces complex biomolecular machines (e.g., ribosomes and telomerases) that represent some of the most daunting targets for biomolecular design. Despite significant advances in protein and DNA or RNA nanotechnology, the construction of artificial nucleoprotein complexes has largely been limited to cases that rely on the NA-mediated spatial organization of protein units, rather than a cooperative interplay between protein- and NA-mediated interactions that typify natural nucleoprotein assemblies. We report here a structurally well-defined synthetic nucleoprotein assembly that forms through the synergy of three types of intermolecular interactions: Watson-Crick base pairing, NA-protein interactions, and protein-metal coordination. The fine thermodynamic balance between these interactions enables the formation of a crystalline architecture under highly specific conditions.
Pubmed
Web of science
Open Access
Oui
Création de la notice
09/06/2023 15:02
Dernière modification de la notice
08/07/2023 5:50
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