| Literature DB >> 35417013 |
Landon Zarowny1, Damien Clavel2, Ryan Johannson1, Kévin Duarte2, Hadrien Depernet3, Jérôme Dupuy2, Heather Baker1, Alex Brown1, Antoine Royant2,3, Robert E Campbell1,4.
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.Entities:
Keywords: crystal structure; fluorescence microscopy; fluorescent protein; protein engineering; tryptophan-derived chromophore
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Year: 2022 PMID: 35417013 PMCID: PMC9083105 DOI: 10.1093/protein/gzac004
Source DB: PubMed Journal: Protein Eng Des Sel ISSN: 1741-0126 Impact factor: 1.952