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Recording of cellular physiological histories along optically readable self-assembling protein chains
Observing cellular physiological histories is key to understanding normal and disease-related processes. Here we describe expression recording islands—a fully genetically encoded approach that enables both continual digital recording of biological information within cells and subsequent high-through...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188365/ https://www.ncbi.nlm.nih.gov/pubmed/36593405 http://dx.doi.org/10.1038/s41587-022-01586-7 |
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author | Linghu, Changyang An, Bobae Shpokayte, Monika Celiker, Orhan T. Shmoel, Nava Zhang, Ruihan Zhang, Chi Park, Demian Park, Won Min Ramirez, Steve Boyden, Edward S. |
author_facet | Linghu, Changyang An, Bobae Shpokayte, Monika Celiker, Orhan T. Shmoel, Nava Zhang, Ruihan Zhang, Chi Park, Demian Park, Won Min Ramirez, Steve Boyden, Edward S. |
author_sort | Linghu, Changyang |
collection | PubMed |
description | Observing cellular physiological histories is key to understanding normal and disease-related processes. Here we describe expression recording islands—a fully genetically encoded approach that enables both continual digital recording of biological information within cells and subsequent high-throughput readout in fixed cells. The information is stored in growing intracellular protein chains made of self-assembling subunits, human-designed filament-forming proteins bearing different epitope tags that each correspond to a different cellular state or function (for example, gene expression downstream of neural activity or pharmacological exposure), allowing the physiological history to be read out along the ordered subunits of protein chains with conventional optical microscopy. We use expression recording islands to record gene expression timecourse downstream of specific pharmacological and physiological stimuli in cultured neurons and in living mouse brain, with a time resolution of a fraction of a day, over periods of days to weeks. |
format | Online Article Text |
id | pubmed-10188365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101883652023-05-18 Recording of cellular physiological histories along optically readable self-assembling protein chains Linghu, Changyang An, Bobae Shpokayte, Monika Celiker, Orhan T. Shmoel, Nava Zhang, Ruihan Zhang, Chi Park, Demian Park, Won Min Ramirez, Steve Boyden, Edward S. Nat Biotechnol Article Observing cellular physiological histories is key to understanding normal and disease-related processes. Here we describe expression recording islands—a fully genetically encoded approach that enables both continual digital recording of biological information within cells and subsequent high-throughput readout in fixed cells. The information is stored in growing intracellular protein chains made of self-assembling subunits, human-designed filament-forming proteins bearing different epitope tags that each correspond to a different cellular state or function (for example, gene expression downstream of neural activity or pharmacological exposure), allowing the physiological history to be read out along the ordered subunits of protein chains with conventional optical microscopy. We use expression recording islands to record gene expression timecourse downstream of specific pharmacological and physiological stimuli in cultured neurons and in living mouse brain, with a time resolution of a fraction of a day, over periods of days to weeks. Nature Publishing Group US 2023-01-02 2023 /pmc/articles/PMC10188365/ /pubmed/36593405 http://dx.doi.org/10.1038/s41587-022-01586-7 Text en © The Author(s) 2023 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 Linghu, Changyang An, Bobae Shpokayte, Monika Celiker, Orhan T. Shmoel, Nava Zhang, Ruihan Zhang, Chi Park, Demian Park, Won Min Ramirez, Steve Boyden, Edward S. Recording of cellular physiological histories along optically readable self-assembling protein chains |
title | Recording of cellular physiological histories along optically readable self-assembling protein chains |
title_full | Recording of cellular physiological histories along optically readable self-assembling protein chains |
title_fullStr | Recording of cellular physiological histories along optically readable self-assembling protein chains |
title_full_unstemmed | Recording of cellular physiological histories along optically readable self-assembling protein chains |
title_short | Recording of cellular physiological histories along optically readable self-assembling protein chains |
title_sort | recording of cellular physiological histories along optically readable self-assembling protein chains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188365/ https://www.ncbi.nlm.nih.gov/pubmed/36593405 http://dx.doi.org/10.1038/s41587-022-01586-7 |
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