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hνSABR: Photochemical Dose–Response Bead Screening in Droplets
[Image: see text] With the potential for each droplet to act as a unique reaction vessel, droplet microfluidics is a powerful tool for high-throughput discovery. Any attempt at compound screening miniaturization must address the significant scaling inefficiencies associated with library handling and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776284/ https://www.ncbi.nlm.nih.gov/pubmed/26815064 http://dx.doi.org/10.1021/acs.analchem.5b04811 |
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author | Price, Alexander K. MacConnell, Andrew B. Paegel, Brian M. |
author_facet | Price, Alexander K. MacConnell, Andrew B. Paegel, Brian M. |
author_sort | Price, Alexander K. |
collection | PubMed |
description | [Image: see text] With the potential for each droplet to act as a unique reaction vessel, droplet microfluidics is a powerful tool for high-throughput discovery. Any attempt at compound screening miniaturization must address the significant scaling inefficiencies associated with library handling and distribution. Eschewing microplate-based compound collections for one-bead-one-compound (OBOC) combinatorial libraries, we have developed hνSABR (Light-Induced and -Graduated High-Throughput Screening After Bead Release), a microfluidic architecture that integrates a suspension hopper for compound library bead introduction, droplet generation, microfabricated waveguides to deliver UV light to the droplet flow for photochemical compound dosing, incubation, and laser-induced fluorescence for assay readout. Avobenzone-doped PDMS (0.6% w/w) patterning confines UV exposure to the desired illumination region, generating intradroplet compound concentrations (>10 μM) that are reproducible between devices. Beads displaying photochemically cleavable pepstatin A were distributed into droplets and exposed with five different UV intensities to demonstrate dose–response screening in an HIV-1 protease activity assay. This microfluidic architecture introduces a new analytical approach for OBOC library screening, and represents a key component of a next-generation distributed small molecule discovery platform. |
format | Online Article Text |
id | pubmed-4776284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47762842016-03-07 hνSABR: Photochemical Dose–Response Bead Screening in Droplets Price, Alexander K. MacConnell, Andrew B. Paegel, Brian M. Anal Chem [Image: see text] With the potential for each droplet to act as a unique reaction vessel, droplet microfluidics is a powerful tool for high-throughput discovery. Any attempt at compound screening miniaturization must address the significant scaling inefficiencies associated with library handling and distribution. Eschewing microplate-based compound collections for one-bead-one-compound (OBOC) combinatorial libraries, we have developed hνSABR (Light-Induced and -Graduated High-Throughput Screening After Bead Release), a microfluidic architecture that integrates a suspension hopper for compound library bead introduction, droplet generation, microfabricated waveguides to deliver UV light to the droplet flow for photochemical compound dosing, incubation, and laser-induced fluorescence for assay readout. Avobenzone-doped PDMS (0.6% w/w) patterning confines UV exposure to the desired illumination region, generating intradroplet compound concentrations (>10 μM) that are reproducible between devices. Beads displaying photochemically cleavable pepstatin A were distributed into droplets and exposed with five different UV intensities to demonstrate dose–response screening in an HIV-1 protease activity assay. This microfluidic architecture introduces a new analytical approach for OBOC library screening, and represents a key component of a next-generation distributed small molecule discovery platform. American Chemical Society 2016-01-27 2016-03-01 /pmc/articles/PMC4776284/ /pubmed/26815064 http://dx.doi.org/10.1021/acs.analchem.5b04811 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Price, Alexander K. MacConnell, Andrew B. Paegel, Brian M. hνSABR: Photochemical Dose–Response Bead Screening in Droplets |
title | hνSABR: Photochemical
Dose–Response Bead Screening in Droplets |
title_full | hνSABR: Photochemical
Dose–Response Bead Screening in Droplets |
title_fullStr | hνSABR: Photochemical
Dose–Response Bead Screening in Droplets |
title_full_unstemmed | hνSABR: Photochemical
Dose–Response Bead Screening in Droplets |
title_short | hνSABR: Photochemical
Dose–Response Bead Screening in Droplets |
title_sort | hνsabr: photochemical
dose–response bead screening in droplets |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776284/ https://www.ncbi.nlm.nih.gov/pubmed/26815064 http://dx.doi.org/10.1021/acs.analchem.5b04811 |
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