Cyan fluorescent proteins derived from mNeonGreen

Author:

Zarowny Landon1,Clavel Damien2,Johannson Ryan1ORCID,Duarte Kévin2,Depernet Hadrien3,Dupuy Jérôme2,Baker Heather1,Brown Alex1ORCID,Royant Antoine23,Campbell Robert E14ORCID

Affiliation:

1. Department of Chemistry, University of Alberta, Edmonton T6G 2G2, Canada

2. Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale (IBS), 38000 Grenoble, France

3. Structural Biology Group, European Synchrotron Radiation Facility, 38043 Grenoble, France

4. Department of Chemistry, University of Tokyo, Tokyo 113-0033, Japan

Abstract

Abstract mNeonGreen, an engineered green fluorescent protein (GFP) derived from lancelet, is one of the most brightly fluorescent homologs of Aequorea victoria jellyfish GFP (avGFP) yet reported. In this work, we investigated whether this bright fluorescence might be retained in homologs of mNeonGreen with modified chromophore structures and altered fluorescent hues. We found mNeonGreen to be generally less tolerant than avGFP to chromophore modification by substitution of the key chromophore-forming tyrosine residue with other aromatic amino acids. However, we were ultimately successful in creating a variant, designated as NeonCyan1, with a tryptophan-derived cyan fluorescent protein (CFP)-type chromophore, and two additional mutants with distinct spectral hues. Structural, computational, and photophysical characterization of NeonCyan1 and its variants provided insight into the factors that control the fluorescence emission color. Though not recommended as replacements for contemporary CFP variants, we demonstrate that NeonCyan1 variants are potentially suitable for live cell imaging applications.

Funder

French Agence Nationale de la Recherche

National Institutes of Health

Natural Sciences and Engineering Research Council

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,Bioengineering,Biotechnology

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