Chromophore Deprotonation State Alters the Optical Properties of Blue Chromoprotein.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 26218063.
- Also identified by DOI 10.1371/journal.pone.0134108 and PMC identifier 4517874.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Chromoproteins (CPs) have unique colors and can be used in biological applications. In this work, a novel blue CP with a maximum absorption peak (λmax) at 608 nm was identified from the carpet anemone Stichodactyla gigantea (sgBP). In vivo expression of sgBP in zebrafish would change the appearance of the fishes to have a blue color, indicating the potential biomarker function. To enhance the color properties, the crystal structure of sgBP at 2.25 Å resolution was determined to allow structure-based protein engineering. Among the mutations conducted in the Gln-Tyr-Gly chromophore and chromophore environment, a S157C mutation shifted the λmax to 604 nm with an extinction coefficient (ε) of 58,029 M-1·cm-1 and darkened the blue color expression. The S157C mutation in the sgBP chromophore environment could affect the color expression by altering the deprotonation state of the phenolic group in the chromophore. Our results provide a structural basis for the blue color enhancement of the biomarker development.
Medical subject headings
- Green Fluorescent Proteins
- Luminescent Proteins
- Pigments, Biological
- Protein Engineering
- Sea Anemones
- Zebrafish