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Multiplex Protein Imaging through PACIFIC: Photoactive Immunofluorescence with Iterative Cleavage
[Image: see text] Multiplex protein imaging technologies enable deep phenotyping and provide rich spatial information about biological samples. Existing methods have shown great success but also harbored trade-offs between various pros and cons, underscoring the persisting necessity to expand the im...
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/PMC10288499/ https://www.ncbi.nlm.nih.gov/pubmed/37363079 http://dx.doi.org/10.1021/acsbiomedchemau.3c00018 |
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author | Ji, Fei Hur, Moises Hur, Sungwon Wang, Siwen Sarkar, Priyanka Shao, Shiqun Aispuro, Desiree Cong, Xu Hu, Yanhao Li, Zhonghan Xue, Min |
author_facet | Ji, Fei Hur, Moises Hur, Sungwon Wang, Siwen Sarkar, Priyanka Shao, Shiqun Aispuro, Desiree Cong, Xu Hu, Yanhao Li, Zhonghan Xue, Min |
author_sort | Ji, Fei |
collection | PubMed |
description | [Image: see text] Multiplex protein imaging technologies enable deep phenotyping and provide rich spatial information about biological samples. Existing methods have shown great success but also harbored trade-offs between various pros and cons, underscoring the persisting necessity to expand the imaging toolkits. Here we present PACIFIC: photoactive immunofluorescence with iterative cleavage, a new modality of multiplex protein imaging methods. PACIFIC achieves iterative multiplexing by implementing photocleavable fluorophores for antibody labeling with one-step spin-column purification. PACIFIC requires no specialized instrument, no DNA encoding, or chemical treatments. We demonstrate that PACIFIC can resolve cellular heterogeneity in both formalin-fixed paraffin-embedded (FFPE) samples and fixed cells. To further highlight how PACIFIC assists discovery, we integrate PACIFIC with live-cell tracking and identify phosphor-p70S6K as a critical driver that governs U87 cell mobility. Considering the cost, flexibility, and compatibility, we foresee that PACIFIC can confer deep phenotyping capabilities to anyone with access to traditional immunofluorescence platforms. |
format | Online Article Text |
id | pubmed-10288499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102884992023-06-24 Multiplex Protein Imaging through PACIFIC: Photoactive Immunofluorescence with Iterative Cleavage Ji, Fei Hur, Moises Hur, Sungwon Wang, Siwen Sarkar, Priyanka Shao, Shiqun Aispuro, Desiree Cong, Xu Hu, Yanhao Li, Zhonghan Xue, Min ACS Bio Med Chem Au [Image: see text] Multiplex protein imaging technologies enable deep phenotyping and provide rich spatial information about biological samples. Existing methods have shown great success but also harbored trade-offs between various pros and cons, underscoring the persisting necessity to expand the imaging toolkits. Here we present PACIFIC: photoactive immunofluorescence with iterative cleavage, a new modality of multiplex protein imaging methods. PACIFIC achieves iterative multiplexing by implementing photocleavable fluorophores for antibody labeling with one-step spin-column purification. PACIFIC requires no specialized instrument, no DNA encoding, or chemical treatments. We demonstrate that PACIFIC can resolve cellular heterogeneity in both formalin-fixed paraffin-embedded (FFPE) samples and fixed cells. To further highlight how PACIFIC assists discovery, we integrate PACIFIC with live-cell tracking and identify phosphor-p70S6K as a critical driver that governs U87 cell mobility. Considering the cost, flexibility, and compatibility, we foresee that PACIFIC can confer deep phenotyping capabilities to anyone with access to traditional immunofluorescence platforms. American Chemical Society 2023-04-28 /pmc/articles/PMC10288499/ /pubmed/37363079 http://dx.doi.org/10.1021/acsbiomedchemau.3c00018 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ji, Fei Hur, Moises Hur, Sungwon Wang, Siwen Sarkar, Priyanka Shao, Shiqun Aispuro, Desiree Cong, Xu Hu, Yanhao Li, Zhonghan Xue, Min Multiplex Protein Imaging through PACIFIC: Photoactive Immunofluorescence with Iterative Cleavage |
title | Multiplex Protein Imaging through PACIFIC: Photoactive
Immunofluorescence with Iterative Cleavage |
title_full | Multiplex Protein Imaging through PACIFIC: Photoactive
Immunofluorescence with Iterative Cleavage |
title_fullStr | Multiplex Protein Imaging through PACIFIC: Photoactive
Immunofluorescence with Iterative Cleavage |
title_full_unstemmed | Multiplex Protein Imaging through PACIFIC: Photoactive
Immunofluorescence with Iterative Cleavage |
title_short | Multiplex Protein Imaging through PACIFIC: Photoactive
Immunofluorescence with Iterative Cleavage |
title_sort | multiplex protein imaging through pacific: photoactive
immunofluorescence with iterative cleavage |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288499/ https://www.ncbi.nlm.nih.gov/pubmed/37363079 http://dx.doi.org/10.1021/acsbiomedchemau.3c00018 |
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