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Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages

[Image: see text] Self-assembly is a convenient process to arrange complex biomolecules into large hierarchically ordered structures. Electrostatic attraction between the building blocks is a particularly interesting driving force for the assembly process, as it is easily tunable and reversible. Lar...

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Autores principales: Korpi, Antti, Ma, Chao, Liu, Kai, Nonappa, Herrmann, Andreas, Ikkala, Olli, Kostiainen, Mauri A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156108/
https://www.ncbi.nlm.nih.gov/pubmed/30271674
http://dx.doi.org/10.1021/acsmacrolett.8b00023
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author Korpi, Antti
Ma, Chao
Liu, Kai
Nonappa,
Herrmann, Andreas
Ikkala, Olli
Kostiainen, Mauri A.
author_facet Korpi, Antti
Ma, Chao
Liu, Kai
Nonappa,
Herrmann, Andreas
Ikkala, Olli
Kostiainen, Mauri A.
author_sort Korpi, Antti
collection PubMed
description [Image: see text] Self-assembly is a convenient process to arrange complex biomolecules into large hierarchically ordered structures. Electrostatic attraction between the building blocks is a particularly interesting driving force for the assembly process, as it is easily tunable and reversible. Large biomolecules with high surface charge density, such as proteins and protein cages, are very promising building blocks due to their uniform size and shape. Assemblies of functional molecules with well-defined nanostructures have wide-ranging applications but are difficult to produce precisely by synthetic methods. Furthermore, obtaining highly ordered structures is an important prerequisite for X-ray structure analysis. Here we show how negatively charged ferritin and viral protein cages can adopt specific cocrystal structures with supercharged cationic polypeptides (SUPs, K72) and their recombinant fusions with green fluorescent protein (GFP-K72). The cage structures and recombinant proteins self-assemble in aqueous solution to large ordered structures, where the structure morphology and size are controlled by the ratio of oppositely charged building blocks and the electrolyte concentration. Both ferritin and viral cages form cocrystals with face centered cubic structure and lattice constants of 14.0 and 28.5 nm, respectively. The crystals are porous and the cationic recombinant proteins occupy the voids between the cages. Such systems resemble naturally occurring occlusion bodies and may serve as protecting agents as well as aid the structure determination of biomolecules by X-ray scattering.
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spelling pubmed-61561082018-09-27 Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages Korpi, Antti Ma, Chao Liu, Kai Nonappa, Herrmann, Andreas Ikkala, Olli Kostiainen, Mauri A. ACS Macro Lett [Image: see text] Self-assembly is a convenient process to arrange complex biomolecules into large hierarchically ordered structures. Electrostatic attraction between the building blocks is a particularly interesting driving force for the assembly process, as it is easily tunable and reversible. Large biomolecules with high surface charge density, such as proteins and protein cages, are very promising building blocks due to their uniform size and shape. Assemblies of functional molecules with well-defined nanostructures have wide-ranging applications but are difficult to produce precisely by synthetic methods. Furthermore, obtaining highly ordered structures is an important prerequisite for X-ray structure analysis. Here we show how negatively charged ferritin and viral protein cages can adopt specific cocrystal structures with supercharged cationic polypeptides (SUPs, K72) and their recombinant fusions with green fluorescent protein (GFP-K72). The cage structures and recombinant proteins self-assemble in aqueous solution to large ordered structures, where the structure morphology and size are controlled by the ratio of oppositely charged building blocks and the electrolyte concentration. Both ferritin and viral cages form cocrystals with face centered cubic structure and lattice constants of 14.0 and 28.5 nm, respectively. The crystals are porous and the cationic recombinant proteins occupy the voids between the cages. Such systems resemble naturally occurring occlusion bodies and may serve as protecting agents as well as aid the structure determination of biomolecules by X-ray scattering. American Chemical Society 2018-02-19 2018-03-20 /pmc/articles/PMC6156108/ /pubmed/30271674 http://dx.doi.org/10.1021/acsmacrolett.8b00023 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Korpi, Antti
Ma, Chao
Liu, Kai
Nonappa,
Herrmann, Andreas
Ikkala, Olli
Kostiainen, Mauri A.
Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages
title Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages
title_full Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages
title_fullStr Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages
title_full_unstemmed Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages
title_short Self-Assembly of Electrostatic Cocrystals from Supercharged Fusion Peptides and Protein Cages
title_sort self-assembly of electrostatic cocrystals from supercharged fusion peptides and protein cages
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156108/
https://www.ncbi.nlm.nih.gov/pubmed/30271674
http://dx.doi.org/10.1021/acsmacrolett.8b00023
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