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Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes

Liquid-solid transition, also known as gelation, is a specific form of phase separation in which molecules cross-link to form a highly interconnected compartment with solid – like dynamical properties. Here, we utilize RNA hairpin coat-protein binding sites to form synthetic RNA based gel-like granu...

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Autores principales: Granik, Naor, Katz, Noa, Willinger, Or, Goldberg, Sarah, Amit, Roee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649756/
https://www.ncbi.nlm.nih.gov/pubmed/36357399
http://dx.doi.org/10.1038/s41467-022-34644-4
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author Granik, Naor
Katz, Noa
Willinger, Or
Goldberg, Sarah
Amit, Roee
author_facet Granik, Naor
Katz, Noa
Willinger, Or
Goldberg, Sarah
Amit, Roee
author_sort Granik, Naor
collection PubMed
description Liquid-solid transition, also known as gelation, is a specific form of phase separation in which molecules cross-link to form a highly interconnected compartment with solid – like dynamical properties. Here, we utilize RNA hairpin coat-protein binding sites to form synthetic RNA based gel-like granules via liquid-solid phase transition. We show both in-vitro and in-vivo that hairpin containing synthetic long non-coding RNA (slncRNA) molecules granulate into bright localized puncta. We further demonstrate that upon introduction of the coat-proteins, less-condensed gel-like granules form with the RNA creating an outer shell with the proteins mostly present inside the granule. Moreover, by tracking puncta fluorescence signals over time, we detected addition or shedding events of slncRNA-CP nucleoprotein complexes. Consequently, our granules constitute a genetically encoded storage compartment for protein and RNA with a programmable controlled release profile that is determined by the number of hairpins encoded into the RNA. Our findings have important implications for the potential regulatory role of naturally occurring granules and for the broader biotechnology field.
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spelling pubmed-96497562022-11-15 Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes Granik, Naor Katz, Noa Willinger, Or Goldberg, Sarah Amit, Roee Nat Commun Article Liquid-solid transition, also known as gelation, is a specific form of phase separation in which molecules cross-link to form a highly interconnected compartment with solid – like dynamical properties. Here, we utilize RNA hairpin coat-protein binding sites to form synthetic RNA based gel-like granules via liquid-solid phase transition. We show both in-vitro and in-vivo that hairpin containing synthetic long non-coding RNA (slncRNA) molecules granulate into bright localized puncta. We further demonstrate that upon introduction of the coat-proteins, less-condensed gel-like granules form with the RNA creating an outer shell with the proteins mostly present inside the granule. Moreover, by tracking puncta fluorescence signals over time, we detected addition or shedding events of slncRNA-CP nucleoprotein complexes. Consequently, our granules constitute a genetically encoded storage compartment for protein and RNA with a programmable controlled release profile that is determined by the number of hairpins encoded into the RNA. Our findings have important implications for the potential regulatory role of naturally occurring granules and for the broader biotechnology field. Nature Publishing Group UK 2022-11-10 /pmc/articles/PMC9649756/ /pubmed/36357399 http://dx.doi.org/10.1038/s41467-022-34644-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Granik, Naor
Katz, Noa
Willinger, Or
Goldberg, Sarah
Amit, Roee
Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes
title Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes
title_full Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes
title_fullStr Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes
title_full_unstemmed Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes
title_short Formation of synthetic RNA protein granules using engineered phage-coat-protein -RNA complexes
title_sort formation of synthetic rna protein granules using engineered phage-coat-protein -rna complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649756/
https://www.ncbi.nlm.nih.gov/pubmed/36357399
http://dx.doi.org/10.1038/s41467-022-34644-4
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