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Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology

Molecular engineering of the green fluorescent protein (GFP) into a robust and stable variant named Superfolder GFP (sfGFP) has revolutionized the field of biosensor development and the use of fluorescent markers in diverse area of biology. sfGFP-based self-associating bipartite split-FP systems hav...

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Detalles Bibliográficos
Autores principales: Pedelacq, Jean-Denis, Cabantous, Stéphanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678664/
https://www.ncbi.nlm.nih.gov/pubmed/31311175
http://dx.doi.org/10.3390/ijms20143479
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author Pedelacq, Jean-Denis
Cabantous, Stéphanie
author_facet Pedelacq, Jean-Denis
Cabantous, Stéphanie
author_sort Pedelacq, Jean-Denis
collection PubMed
description Molecular engineering of the green fluorescent protein (GFP) into a robust and stable variant named Superfolder GFP (sfGFP) has revolutionized the field of biosensor development and the use of fluorescent markers in diverse area of biology. sfGFP-based self-associating bipartite split-FP systems have been widely exploited to monitor soluble expression in vitro, localization, and trafficking of proteins in cellulo. A more recent class of split-FP variants, named « tripartite » split-FP, that rely on the self-assembly of three GFP fragments, is particularly well suited for the detection of protein–protein interactions. In this review, we describe the different steps and evolutions that have led to the diversification of superfolder and split-FP reporter systems, and we report an update of their applications in various areas of biology, from structural biology to cell biology.
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spelling pubmed-66786642019-08-19 Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology Pedelacq, Jean-Denis Cabantous, Stéphanie Int J Mol Sci Review Molecular engineering of the green fluorescent protein (GFP) into a robust and stable variant named Superfolder GFP (sfGFP) has revolutionized the field of biosensor development and the use of fluorescent markers in diverse area of biology. sfGFP-based self-associating bipartite split-FP systems have been widely exploited to monitor soluble expression in vitro, localization, and trafficking of proteins in cellulo. A more recent class of split-FP variants, named « tripartite » split-FP, that rely on the self-assembly of three GFP fragments, is particularly well suited for the detection of protein–protein interactions. In this review, we describe the different steps and evolutions that have led to the diversification of superfolder and split-FP reporter systems, and we report an update of their applications in various areas of biology, from structural biology to cell biology. MDPI 2019-07-15 /pmc/articles/PMC6678664/ /pubmed/31311175 http://dx.doi.org/10.3390/ijms20143479 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pedelacq, Jean-Denis
Cabantous, Stéphanie
Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology
title Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology
title_full Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology
title_fullStr Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology
title_full_unstemmed Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology
title_short Development and Applications of Superfolder and Split Fluorescent Protein Detection Systems in Biology
title_sort development and applications of superfolder and split fluorescent protein detection systems in biology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678664/
https://www.ncbi.nlm.nih.gov/pubmed/31311175
http://dx.doi.org/10.3390/ijms20143479
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