Cargando…

Rapid two-dimensional characterisation of proteins in solution

Microfluidic platforms provide an excellent basis for working with heterogeneous samples and separating biomolecular components at high throughput, with high recovery rates and by using only very small sample volumes. To date, several micron scale platforms with preparative capabilities have been de...

Descripción completa

Detalles Bibliográficos
Autores principales: Saar, Kadi L., Peter, Quentin, Müller, Thomas, Challa, Pavan K., Herling, Therese W., Knowles, Tuomas P. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799820/
https://www.ncbi.nlm.nih.gov/pubmed/31636924
http://dx.doi.org/10.1038/s41378-019-0072-3
_version_ 1783460373248081920
author Saar, Kadi L.
Peter, Quentin
Müller, Thomas
Challa, Pavan K.
Herling, Therese W.
Knowles, Tuomas P. J.
author_facet Saar, Kadi L.
Peter, Quentin
Müller, Thomas
Challa, Pavan K.
Herling, Therese W.
Knowles, Tuomas P. J.
author_sort Saar, Kadi L.
collection PubMed
description Microfluidic platforms provide an excellent basis for working with heterogeneous samples and separating biomolecular components at high throughput, with high recovery rates and by using only very small sample volumes. To date, several micron scale platforms with preparative capabilities have been demonstrated. Here we describe and demonstrate a microfluidic device that brings preparative and analytical operations together onto a single chip and thereby allows the acquisition of multidimensional information. We achieve this objective by using a free-flow electrophoretic separation approach that directs fractions of sample into an on-chip analysis unit, where the fractions are characterised through a microfluidic diffusional sizing process. This combined approach therefore allows simultaneously quantifying the sizes and the charges of components in heterogenous mixtures. We illustrate the power of the platform by describing the size distribution of a mixture comprising components which are close in size and cannot be identified as individual components using state-of-the-art solution sizing techniques on their own. Furthermore, we show that the platform can be used for two-dimensional fingerprinting of heterogeneous protein mixtures within tens of seconds, opening up a possibility to obtain multiparameter data on biomolecular systems on a minute timescale.
format Online
Article
Text
id pubmed-6799820
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-67998202019-10-21 Rapid two-dimensional characterisation of proteins in solution Saar, Kadi L. Peter, Quentin Müller, Thomas Challa, Pavan K. Herling, Therese W. Knowles, Tuomas P. J. Microsyst Nanoeng Article Microfluidic platforms provide an excellent basis for working with heterogeneous samples and separating biomolecular components at high throughput, with high recovery rates and by using only very small sample volumes. To date, several micron scale platforms with preparative capabilities have been demonstrated. Here we describe and demonstrate a microfluidic device that brings preparative and analytical operations together onto a single chip and thereby allows the acquisition of multidimensional information. We achieve this objective by using a free-flow electrophoretic separation approach that directs fractions of sample into an on-chip analysis unit, where the fractions are characterised through a microfluidic diffusional sizing process. This combined approach therefore allows simultaneously quantifying the sizes and the charges of components in heterogenous mixtures. We illustrate the power of the platform by describing the size distribution of a mixture comprising components which are close in size and cannot be identified as individual components using state-of-the-art solution sizing techniques on their own. Furthermore, we show that the platform can be used for two-dimensional fingerprinting of heterogeneous protein mixtures within tens of seconds, opening up a possibility to obtain multiparameter data on biomolecular systems on a minute timescale. Nature Publishing Group UK 2019-07-01 /pmc/articles/PMC6799820/ /pubmed/31636924 http://dx.doi.org/10.1038/s41378-019-0072-3 Text en © The Author(s) 2019 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
Saar, Kadi L.
Peter, Quentin
Müller, Thomas
Challa, Pavan K.
Herling, Therese W.
Knowles, Tuomas P. J.
Rapid two-dimensional characterisation of proteins in solution
title Rapid two-dimensional characterisation of proteins in solution
title_full Rapid two-dimensional characterisation of proteins in solution
title_fullStr Rapid two-dimensional characterisation of proteins in solution
title_full_unstemmed Rapid two-dimensional characterisation of proteins in solution
title_short Rapid two-dimensional characterisation of proteins in solution
title_sort rapid two-dimensional characterisation of proteins in solution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799820/
https://www.ncbi.nlm.nih.gov/pubmed/31636924
http://dx.doi.org/10.1038/s41378-019-0072-3
work_keys_str_mv AT saarkadil rapidtwodimensionalcharacterisationofproteinsinsolution
AT peterquentin rapidtwodimensionalcharacterisationofproteinsinsolution
AT mullerthomas rapidtwodimensionalcharacterisationofproteinsinsolution
AT challapavank rapidtwodimensionalcharacterisationofproteinsinsolution
AT herlingtheresew rapidtwodimensionalcharacterisationofproteinsinsolution
AT knowlestuomaspj rapidtwodimensionalcharacterisationofproteinsinsolution