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De Novo Designed Heterochiral Blue Fluorescent Protein
[Image: see text] Diversification of chain stereochemistry offers a tremendous increase in protein design space. We have designed a minimal fluorescent protein, pregnant with β-(1-azulenyl)-l-alanine in the hydrophobic core of a heterotactic protein scaffold, employing automated design tools such as...
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/PMC7581079/ https://www.ncbi.nlm.nih.gov/pubmed/33110966 http://dx.doi.org/10.1021/acsomega.0c02574 |
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author | Prakash, Vivek Ranbhor, Ranjit Ramakrishnan, Vibin |
author_facet | Prakash, Vivek Ranbhor, Ranjit Ramakrishnan, Vibin |
author_sort | Prakash, Vivek |
collection | PubMed |
description | [Image: see text] Diversification of chain stereochemistry offers a tremendous increase in protein design space. We have designed a minimal fluorescent protein, pregnant with β-(1-azulenyl)-l-alanine in the hydrophobic core of a heterotactic protein scaffold, employing automated design tools such as automated repetitive simulated annealing molecular dynamics and IDeAS. The de novo designed heterochiral protein can be selectively excited at 342 nm, quite distant from the intrinsic fluorophore, and emits in the blue region. The structure and stability of the designed proteins were evaluated by established spectroscopic and calorimetric methods. |
format | Online Article Text |
id | pubmed-7581079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75810792020-10-26 De Novo Designed Heterochiral Blue Fluorescent Protein Prakash, Vivek Ranbhor, Ranjit Ramakrishnan, Vibin ACS Omega [Image: see text] Diversification of chain stereochemistry offers a tremendous increase in protein design space. We have designed a minimal fluorescent protein, pregnant with β-(1-azulenyl)-l-alanine in the hydrophobic core of a heterotactic protein scaffold, employing automated design tools such as automated repetitive simulated annealing molecular dynamics and IDeAS. The de novo designed heterochiral protein can be selectively excited at 342 nm, quite distant from the intrinsic fluorophore, and emits in the blue region. The structure and stability of the designed proteins were evaluated by established spectroscopic and calorimetric methods. American Chemical Society 2020-10-06 /pmc/articles/PMC7581079/ /pubmed/33110966 http://dx.doi.org/10.1021/acsomega.0c02574 Text en © 2020 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 | Prakash, Vivek Ranbhor, Ranjit Ramakrishnan, Vibin De Novo Designed Heterochiral Blue Fluorescent Protein |
title | De
Novo Designed Heterochiral Blue Fluorescent Protein |
title_full | De
Novo Designed Heterochiral Blue Fluorescent Protein |
title_fullStr | De
Novo Designed Heterochiral Blue Fluorescent Protein |
title_full_unstemmed | De
Novo Designed Heterochiral Blue Fluorescent Protein |
title_short | De
Novo Designed Heterochiral Blue Fluorescent Protein |
title_sort | de
novo designed heterochiral blue fluorescent protein |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7581079/ https://www.ncbi.nlm.nih.gov/pubmed/33110966 http://dx.doi.org/10.1021/acsomega.0c02574 |
work_keys_str_mv | AT prakashvivek denovodesignedheterochiralbluefluorescentprotein AT ranbhorranjit denovodesignedheterochiralbluefluorescentprotein AT ramakrishnanvibin denovodesignedheterochiralbluefluorescentprotein |