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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...

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Autores principales: Prakash, Vivek, Ranbhor, Ranjit, Ramakrishnan, Vibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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
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AT ramakrishnanvibin denovodesignedheterochiralbluefluorescentprotein