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Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy
High-resolution structural studies of proteins and protein complexes in a native eukaryotic environment present a challenge to structural biology. In-cell NMR can characterize atomic resolution structures but requires high concentrations of labeled proteins in intact cells. Most exogenous delivery t...
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/PMC9098904/ https://www.ncbi.nlm.nih.gov/pubmed/35551287 http://dx.doi.org/10.1038/s42003-022-03412-x |
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author | Sciolino, Nicholas Liu, Anna Breindel, Leonard Burz, David S. Sulchek, Todd Shekhtman, Alexander |
author_facet | Sciolino, Nicholas Liu, Anna Breindel, Leonard Burz, David S. Sulchek, Todd Shekhtman, Alexander |
author_sort | Sciolino, Nicholas |
collection | PubMed |
description | High-resolution structural studies of proteins and protein complexes in a native eukaryotic environment present a challenge to structural biology. In-cell NMR can characterize atomic resolution structures but requires high concentrations of labeled proteins in intact cells. Most exogenous delivery techniques are limited to specific cell types or are too destructive to preserve cellular physiology. The feasibility of microfluidics transfection or volume exchange for convective transfer, VECT, as a means to deliver labeled target proteins to HeLa cells for in-cell NMR experiments is demonstrated. VECT delivery does not require optimization or impede cell viability; cells are immediately available for long-term eukaryotic in-cell NMR experiments. In-cell NMR-based drug screening using VECT was demonstrated by collecting spectra of the sensor molecule DARPP32, in response to exogenous administration of Forskolin. |
format | Online Article Text |
id | pubmed-9098904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90989042022-05-14 Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy Sciolino, Nicholas Liu, Anna Breindel, Leonard Burz, David S. Sulchek, Todd Shekhtman, Alexander Commun Biol Article High-resolution structural studies of proteins and protein complexes in a native eukaryotic environment present a challenge to structural biology. In-cell NMR can characterize atomic resolution structures but requires high concentrations of labeled proteins in intact cells. Most exogenous delivery techniques are limited to specific cell types or are too destructive to preserve cellular physiology. The feasibility of microfluidics transfection or volume exchange for convective transfer, VECT, as a means to deliver labeled target proteins to HeLa cells for in-cell NMR experiments is demonstrated. VECT delivery does not require optimization or impede cell viability; cells are immediately available for long-term eukaryotic in-cell NMR experiments. In-cell NMR-based drug screening using VECT was demonstrated by collecting spectra of the sensor molecule DARPP32, in response to exogenous administration of Forskolin. Nature Publishing Group UK 2022-05-12 /pmc/articles/PMC9098904/ /pubmed/35551287 http://dx.doi.org/10.1038/s42003-022-03412-x Text en © The Author(s) 2022, corrected publication 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 Sciolino, Nicholas Liu, Anna Breindel, Leonard Burz, David S. Sulchek, Todd Shekhtman, Alexander Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy |
title | Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy |
title_full | Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy |
title_fullStr | Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy |
title_full_unstemmed | Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy |
title_short | Microfluidics delivery of DARPP-32 into HeLa cells maintains viability for in-cell NMR spectroscopy |
title_sort | microfluidics delivery of darpp-32 into hela cells maintains viability for in-cell nmr spectroscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098904/ https://www.ncbi.nlm.nih.gov/pubmed/35551287 http://dx.doi.org/10.1038/s42003-022-03412-x |
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