Bioluminescence of the Ca2+‐binding photoprotein, aequorin, after histidine modification
Yoshihiro Ohmiya, Frederick I. Tsuji
Abstract
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Yoshihiro Ohmiya, Frederick I. Tsuji
Abstract
Open-access reader
Modification studies of the 5 histidine residues in aequorin employing site-directed mutagenesis and diethyl pyrocarbonate suggested that His169 may be the site of binding of molecular oxygen in aequorin. The modification of this residue led to complete loss of activity, whereas modification of the remaining 4 histidine residues yielded mutant aequorins with varying bioluminescence activities.
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Modification studies of the 5 histidine residues in aequorin employing site-directed mutagenesis and diethyl pyrocarbonate suggested that His169 may be the site of binding of molecular oxygen in aequorin. The modification of this residue led to complete loss of activity, whereas modification of the remaining 4 histidine residues yielded mutant aequorins with varying bioluminescence activities.
Key concepts: Aequorin, Photoprotein, Bioluminescence, Histidine, Chemistry, Site-directed mutagenesis, Biochemistry, Mutagenesis