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Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity
Scanning probe microscopy provides a unique window into the morphology, mechanics, and structure of proteins and their complexes on the nanoscale. Such measurements require, however, deposition of samples onto substrates. This process can affect conformations and assembly states of the molecular spe...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155325/ https://www.ncbi.nlm.nih.gov/pubmed/30250131 http://dx.doi.org/10.1038/s41467-018-06345-4 |
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author | Ruggeri, Francesco Simone Charmet, Jerome Kartanas, Tadas Peter, Quentin Chia, Sean Habchi, Johnny Dobson, Christopher M. Vendruscolo, Michele Knowles, Tuomas P. J. |
author_facet | Ruggeri, Francesco Simone Charmet, Jerome Kartanas, Tadas Peter, Quentin Chia, Sean Habchi, Johnny Dobson, Christopher M. Vendruscolo, Michele Knowles, Tuomas P. J. |
author_sort | Ruggeri, Francesco Simone |
collection | PubMed |
description | Scanning probe microscopy provides a unique window into the morphology, mechanics, and structure of proteins and their complexes on the nanoscale. Such measurements require, however, deposition of samples onto substrates. This process can affect conformations and assembly states of the molecular species under investigation and can bias the molecular populations observed in heterogeneous samples through differential adsorption. Here, we show that these limitations can be overcome with a single-step microfluidic spray deposition platform. This method transfers biological solutions to substrates as microdroplets with subpicoliter volume, drying in milliseconds, a timescale that is shorter than typical diffusion times of proteins on liquid–solid interfaces, thus avoiding surface mass transport and change to the assembly state. Finally, the single-step deposition ensures the attachment of the full molecular content of the sample to the substrate, allowing quantitative measurements of different molecular populations within heterogeneous systems, including protein aggregates. |
format | Online Article Text |
id | pubmed-6155325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61553252018-09-28 Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity Ruggeri, Francesco Simone Charmet, Jerome Kartanas, Tadas Peter, Quentin Chia, Sean Habchi, Johnny Dobson, Christopher M. Vendruscolo, Michele Knowles, Tuomas P. J. Nat Commun Article Scanning probe microscopy provides a unique window into the morphology, mechanics, and structure of proteins and their complexes on the nanoscale. Such measurements require, however, deposition of samples onto substrates. This process can affect conformations and assembly states of the molecular species under investigation and can bias the molecular populations observed in heterogeneous samples through differential adsorption. Here, we show that these limitations can be overcome with a single-step microfluidic spray deposition platform. This method transfers biological solutions to substrates as microdroplets with subpicoliter volume, drying in milliseconds, a timescale that is shorter than typical diffusion times of proteins on liquid–solid interfaces, thus avoiding surface mass transport and change to the assembly state. Finally, the single-step deposition ensures the attachment of the full molecular content of the sample to the substrate, allowing quantitative measurements of different molecular populations within heterogeneous systems, including protein aggregates. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155325/ /pubmed/30250131 http://dx.doi.org/10.1038/s41467-018-06345-4 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Ruggeri, Francesco Simone Charmet, Jerome Kartanas, Tadas Peter, Quentin Chia, Sean Habchi, Johnny Dobson, Christopher M. Vendruscolo, Michele Knowles, Tuomas P. J. Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
title | Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
title_full | Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
title_fullStr | Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
title_full_unstemmed | Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
title_short | Microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
title_sort | microfluidic deposition for resolving single-molecule protein architecture and heterogeneity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155325/ https://www.ncbi.nlm.nih.gov/pubmed/30250131 http://dx.doi.org/10.1038/s41467-018-06345-4 |
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