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Coupling Droplet Microfluidics with Mass Spectrometry for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above 30 Hz
[Image: see text] High- and ultrahigh-throughput label-free sample analysis is required by many applications, extending from environmental monitoring to drug discovery and industrial biotechnology. HTS methods predominantly are based on a targeted workflow, which can limit their scope. Mass spectrom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009470/ https://www.ncbi.nlm.nih.gov/pubmed/32786490 http://dx.doi.org/10.1021/acs.analchem.0c02632 |
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author | Kempa, Emily E. Smith, Clive A. Li, Xin Bellina, Bruno Richardson, Keith Pringle, Steven Galman, James L. Turner, Nicholas J. Barran, Perdita E. |
author_facet | Kempa, Emily E. Smith, Clive A. Li, Xin Bellina, Bruno Richardson, Keith Pringle, Steven Galman, James L. Turner, Nicholas J. Barran, Perdita E. |
author_sort | Kempa, Emily E. |
collection | PubMed |
description | [Image: see text] High- and ultrahigh-throughput label-free sample analysis is required by many applications, extending from environmental monitoring to drug discovery and industrial biotechnology. HTS methods predominantly are based on a targeted workflow, which can limit their scope. Mass spectrometry readily provides chemical identity and abundance for complex mixtures, and here, we use microdroplet generation microfluidics to supply picoliter aliquots for analysis at rates up to and including 33 Hz. This is demonstrated for small molecules, peptides, and proteins up to 66 kDa on three commercially available mass spectrometers from salty solutions to mimic cellular environments. Designs for chip-based interfaces that permit this coupling are presented, and the merits and challenges of these interfaces are discussed. On an Orbitrap platform droplet infusion rates of 6 Hz are used for analysis of cytochrome c, on a DTIMS Q-TOF similar rates were obtained, and on a TWIMS Q-TOF utilizing IM-MS software rates up to 33 Hz are demonstrated. The potential of this approach is demonstrated with proof of concept experiments on crude mixtures including egg white, unpurified recombinant protein, and a biotransformation supernatant. |
format | Online Article Text |
id | pubmed-8009470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80094702021-03-31 Coupling Droplet Microfluidics with Mass Spectrometry for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above 30 Hz Kempa, Emily E. Smith, Clive A. Li, Xin Bellina, Bruno Richardson, Keith Pringle, Steven Galman, James L. Turner, Nicholas J. Barran, Perdita E. Anal Chem [Image: see text] High- and ultrahigh-throughput label-free sample analysis is required by many applications, extending from environmental monitoring to drug discovery and industrial biotechnology. HTS methods predominantly are based on a targeted workflow, which can limit their scope. Mass spectrometry readily provides chemical identity and abundance for complex mixtures, and here, we use microdroplet generation microfluidics to supply picoliter aliquots for analysis at rates up to and including 33 Hz. This is demonstrated for small molecules, peptides, and proteins up to 66 kDa on three commercially available mass spectrometers from salty solutions to mimic cellular environments. Designs for chip-based interfaces that permit this coupling are presented, and the merits and challenges of these interfaces are discussed. On an Orbitrap platform droplet infusion rates of 6 Hz are used for analysis of cytochrome c, on a DTIMS Q-TOF similar rates were obtained, and on a TWIMS Q-TOF utilizing IM-MS software rates up to 33 Hz are demonstrated. The potential of this approach is demonstrated with proof of concept experiments on crude mixtures including egg white, unpurified recombinant protein, and a biotransformation supernatant. American Chemical Society 2020-07-30 2020-09-15 /pmc/articles/PMC8009470/ /pubmed/32786490 http://dx.doi.org/10.1021/acs.analchem.0c02632 Text en 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 | Kempa, Emily E. Smith, Clive A. Li, Xin Bellina, Bruno Richardson, Keith Pringle, Steven Galman, James L. Turner, Nicholas J. Barran, Perdita E. Coupling Droplet Microfluidics with Mass Spectrometry for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above 30 Hz |
title | Coupling Droplet Microfluidics with Mass Spectrometry
for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above
30 Hz |
title_full | Coupling Droplet Microfluidics with Mass Spectrometry
for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above
30 Hz |
title_fullStr | Coupling Droplet Microfluidics with Mass Spectrometry
for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above
30 Hz |
title_full_unstemmed | Coupling Droplet Microfluidics with Mass Spectrometry
for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above
30 Hz |
title_short | Coupling Droplet Microfluidics with Mass Spectrometry
for Ultrahigh-Throughput Analysis of Complex Mixtures up to and above
30 Hz |
title_sort | coupling droplet microfluidics with mass spectrometry
for ultrahigh-throughput analysis of complex mixtures up to and above
30 hz |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009470/ https://www.ncbi.nlm.nih.gov/pubmed/32786490 http://dx.doi.org/10.1021/acs.analchem.0c02632 |
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