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Orthogonal Versatile Interacting Peptide Tags for Imaging Cellular Proteins
[Image: see text] Genetic tags are transformative tools for investigating the function, localization, and interactions of cellular proteins. Most studies today are reliant on selective labeling of more than one protein to obtain comprehensive information on a protein’s behavior in situ. Some protein...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249344/ https://www.ncbi.nlm.nih.gov/pubmed/37167569 http://dx.doi.org/10.1021/acs.biochem.2c00712 |
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author | Suyama, Alexa Devlin, Kaylyn L. Macias-Contreras, Miguel Doh, Julia K. Shinde, Ujwal Beatty, Kimberly E. |
author_facet | Suyama, Alexa Devlin, Kaylyn L. Macias-Contreras, Miguel Doh, Julia K. Shinde, Ujwal Beatty, Kimberly E. |
author_sort | Suyama, Alexa |
collection | PubMed |
description | [Image: see text] Genetic tags are transformative tools for investigating the function, localization, and interactions of cellular proteins. Most studies today are reliant on selective labeling of more than one protein to obtain comprehensive information on a protein’s behavior in situ. Some proteins can be analyzed by fusion to a protein tag, such as green fluorescent protein, HaloTag, or SNAP-Tag. Other proteins benefit from labeling via small peptide tags, such as the recently reported versatile interacting peptide (VIP) tags. VIP tags enable observations of protein localization and trafficking with bright fluorophores or nanoparticles. Here, we expand the VIP toolkit by presenting two new tags: TinyVIPER and PunyVIPER. These two tags were designed for use with MiniVIPER for labeling up to three distinct proteins at once in cells. Labeling is mediated by the formation of a high-affinity, biocompatible heterodimeric coiled coil. Each tag was validated by fluorescence microscopy, including observation of transferrin receptor 1 trafficking in live cells. We verified that labeling via each tag is highly specific for one- or two-color imaging. Last, the self-sorting tags were used for simultaneous labeling of three protein targets (i.e., TOMM20, histone 2B, and actin) in fixed cells, highlighting their utility for multicolor microscopy. MiniVIPER, TinyVIPER, and PunyVIPER are small and robust peptide tags for selective labeling of cellular proteins. |
format | Online Article Text |
id | pubmed-10249344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102493442023-06-09 Orthogonal Versatile Interacting Peptide Tags for Imaging Cellular Proteins Suyama, Alexa Devlin, Kaylyn L. Macias-Contreras, Miguel Doh, Julia K. Shinde, Ujwal Beatty, Kimberly E. Biochemistry [Image: see text] Genetic tags are transformative tools for investigating the function, localization, and interactions of cellular proteins. Most studies today are reliant on selective labeling of more than one protein to obtain comprehensive information on a protein’s behavior in situ. Some proteins can be analyzed by fusion to a protein tag, such as green fluorescent protein, HaloTag, or SNAP-Tag. Other proteins benefit from labeling via small peptide tags, such as the recently reported versatile interacting peptide (VIP) tags. VIP tags enable observations of protein localization and trafficking with bright fluorophores or nanoparticles. Here, we expand the VIP toolkit by presenting two new tags: TinyVIPER and PunyVIPER. These two tags were designed for use with MiniVIPER for labeling up to three distinct proteins at once in cells. Labeling is mediated by the formation of a high-affinity, biocompatible heterodimeric coiled coil. Each tag was validated by fluorescence microscopy, including observation of transferrin receptor 1 trafficking in live cells. We verified that labeling via each tag is highly specific for one- or two-color imaging. Last, the self-sorting tags were used for simultaneous labeling of three protein targets (i.e., TOMM20, histone 2B, and actin) in fixed cells, highlighting their utility for multicolor microscopy. MiniVIPER, TinyVIPER, and PunyVIPER are small and robust peptide tags for selective labeling of cellular proteins. American Chemical Society 2023-05-11 /pmc/articles/PMC10249344/ /pubmed/37167569 http://dx.doi.org/10.1021/acs.biochem.2c00712 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Suyama, Alexa Devlin, Kaylyn L. Macias-Contreras, Miguel Doh, Julia K. Shinde, Ujwal Beatty, Kimberly E. Orthogonal Versatile Interacting Peptide Tags for Imaging Cellular Proteins |
title | Orthogonal Versatile
Interacting Peptide Tags for
Imaging Cellular Proteins |
title_full | Orthogonal Versatile
Interacting Peptide Tags for
Imaging Cellular Proteins |
title_fullStr | Orthogonal Versatile
Interacting Peptide Tags for
Imaging Cellular Proteins |
title_full_unstemmed | Orthogonal Versatile
Interacting Peptide Tags for
Imaging Cellular Proteins |
title_short | Orthogonal Versatile
Interacting Peptide Tags for
Imaging Cellular Proteins |
title_sort | orthogonal versatile
interacting peptide tags for
imaging cellular proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249344/ https://www.ncbi.nlm.nih.gov/pubmed/37167569 http://dx.doi.org/10.1021/acs.biochem.2c00712 |
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