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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9649756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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