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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2017
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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. |
format | Online Article Text |
id | pubmed-5788330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT azumayusuke substratesortingbyasuperchargednanoreactor AT baderdaniellv substratesortingbyasuperchargednanoreactor AT hilvertdonald substratesortingbyasuperchargednanoreactor |