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Substrate Sorting by a Supercharged Nanoreactor

[Image: see text] Compartmentalization of proteases enables spatially and temporally controlled protein degradation in cells. Here we show that an engineered lumazine synthase protein cage, which possesses a negatively supercharged lumen, can exploit electrostatic effects to sort substrates for an e...

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Detalles Bibliográficos
Autores principales: Azuma, Yusuke, Bader, Daniel L. V., Hilvert, Donald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788330/
https://www.ncbi.nlm.nih.gov/pubmed/29278496
http://dx.doi.org/10.1021/jacs.7b11210
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author Azuma, Yusuke
Bader, Daniel L. V.
Hilvert, Donald
author_facet Azuma, Yusuke
Bader, Daniel L. V.
Hilvert, Donald
author_sort Azuma, Yusuke
collection PubMed
description [Image: see text] Compartmentalization of proteases enables spatially and temporally controlled protein degradation in cells. Here we show that an engineered lumazine synthase protein cage, which possesses a negatively supercharged lumen, can exploit electrostatic effects to sort substrates for an encapsulated protease. This proteasome-like nanoreactor preferentially cleaves positively charged polypeptides over both anionic and zwitterionic substrates, inverting the inherent substrate specificity of the guest enzyme approximately 480 fold. Our results suggest that supercharged nanochambers could provide a simple and potentially general means of conferring substrate specificity to diverse encapsulated catalysts.
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spelling pubmed-57883302018-01-30 Substrate Sorting by a Supercharged Nanoreactor Azuma, Yusuke Bader, Daniel L. V. Hilvert, Donald J Am Chem Soc [Image: see text] Compartmentalization of proteases enables spatially and temporally controlled protein degradation in cells. Here we show that an engineered lumazine synthase protein cage, which possesses a negatively supercharged lumen, can exploit electrostatic effects to sort substrates for an encapsulated protease. This proteasome-like nanoreactor preferentially cleaves positively charged polypeptides over both anionic and zwitterionic substrates, inverting the inherent substrate specificity of the guest enzyme approximately 480 fold. Our results suggest that supercharged nanochambers could provide a simple and potentially general means of conferring substrate specificity to diverse encapsulated catalysts. American Chemical Society 2017-12-26 2018-01-24 /pmc/articles/PMC5788330/ /pubmed/29278496 http://dx.doi.org/10.1021/jacs.7b11210 Text en Copyright © 2017 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 Azuma, Yusuke
Bader, Daniel L. V.
Hilvert, Donald
Substrate Sorting by a Supercharged Nanoreactor
title Substrate Sorting by a Supercharged Nanoreactor
title_full Substrate Sorting by a Supercharged Nanoreactor
title_fullStr Substrate Sorting by a Supercharged Nanoreactor
title_full_unstemmed Substrate Sorting by a Supercharged Nanoreactor
title_short Substrate Sorting by a Supercharged Nanoreactor
title_sort substrate sorting by a supercharged nanoreactor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788330/
https://www.ncbi.nlm.nih.gov/pubmed/29278496
http://dx.doi.org/10.1021/jacs.7b11210
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