Slow luminescence kinetics of semi-synthetic aequorin: expression, purification and structure determination of cf3-aequorin. (23rd May 2018)

• Record Type: Journal Article
• Authors: Inouye, Satoshi; Tomabechi, Yuri; Hosoya, Takamitsu; Sekine, Shun-ichi; Shirouzu, Mikako
• Is Part Of: Journal of biochemistry. Volume 164:Number 3(2018:Sep.)
• Page Start: 247
• Page End: 255
• Publication Date: 2018-05-23
• Subjects: calcium-binding protein -- EF-hand motif -- photoprotein -- van der Waals interaction -- water molecules; Biochemistry -- Periodicals; Biochemistry -- Periodicals; Electronic journals; 572.05
• DOI: 10.1093/jb/mvy049
• Languages: English
• ISSNs: 0021-924X

Abstract

Abstract: cf3 -Aequorin is one of the semi-synthetic aequorins that was produced by replacing 2-peroxycoelenterazine (CTZ-OOH) in native aequorin with a 2-peroxycoelenterazine analog, and it was prepared using the C2-modified trifluoromethyl analog of coelenterazine ( cf3 -CTZ) and the histidine-tagged apoaequorin expressed in Escherichia coli cells. The purified cf3 -aequorin showed a slow luminescence pattern with half-decay time of maximum intensities of luminescence of 5.0 s. This is much longer than that of 0.9 s for native aequorin, and its luminescence capacity was estimated to be 72.8% of that of native aequorin. The crystal structure of cf3 -aequorin was determined at 2.15 Å resolution. The light source of 2-peroxytrifluoromethylcoelenterazine ( cf3- CTZ-OOH) was stabilized by the hydrogen-bonding interactions at the C2-peroxy moiety and the p -hydroxy moiety at the C6-phenyl group. In native aequorin, three water molecules contribute to stabilizing CTZ-OOH through hydrogen bonds. However, cf3 -aequorin only contained one water molecule, and the trifluoromethyl moiety at the C2-benzyl group of cf3 -CTZ-OOH interacted with the protein by van der Waals interactions. The slow luminescence kinetics of cf3 -aequorin could be explained by slow conformational changes due to the bulkiness of the trifluoromethyl group, which might hinder the smooth cleavage of hydrogen bonds at the C2-peroxy moiety after the binding of Ca 2+ to cf3 -aequorin.