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1 y effect on the luminescence activity of the photoprotein.
2 nophores, is carried out by Ca(2+)-dependent photoproteins.
3 luminescence ordinarily observed from native photoproteins.
4 cells constructed from the purple bacterial photoproteins.
5 aluable insights for future studies of PT in photoproteins.
6 nt dyes, although the use of the recombinant photoprotein aequorin (AEQ) as a Ca(2+) sensor has gaine
8 he most deadly species of malaria, using the photoprotein aequorin as a bioluminescent label has been
10 pecifically, we have prepared mutants of the photoprotein aequorin containing single cysteine residue
12 lecules or peptides to the N-terminus of the photoprotein aequorin such that the binding characterist
15 jellyfish Aequorea victoria consists of the photoprotein aequorin, which contains the molecule coele
21 the AEQ system for cells expressing both the photoprotein and the GPCR target of interest has necessi
23 tability is the architecture surrounding the photoprotein, and that biohybrid sensors and photovoltai
27 , we evaluated aequorin, a calcium-dependent photoprotein, as a potential bioluminescent reporter pro
30 ntitative measurements of a Ca(2+)-activated photoprotein biosensor of recombinant OR function in an
31 s environment were recently shown to contain photoproteins called proteorhodopsins, thought to contri
33 Despite numerous studies on the ctenophore photoprotein family, the detailed catalytic mechanism an
36 Transgenic fish with the Ca(2+)-sensitive photoprotein green fluorescent protein (GFP)-Aequorin in
37 nt molecules to fluorescent biomolecules and photoproteins ingeniously engineered to follow signaling
39 2 and the coelenterazine found in the active photoprotein is preserved at the equivalent position of
40 orage of electrical charge in multilayers of photoproteins isolated from Rhodobacter sphaeroides.
41 inescence reaction in these Ca(2+)-regulated photoproteins may be a shift of the hydrogen bond donor-
42 h bioluminescence spectra obtained from some photoprotein mutants or to populate the lower energy sta
44 as developed on the base of Ca(2+)-regulated photoprotein obelin mutants with altered color and kinet
45 njugate of this aptamer and Ca(2+)-regulated photoprotein obelin was obtained for the first time and
47 s - consisting of ER Ca(2+) depletion during photoprotein reconstitution followed by ER Ca(2+) refill
48 ndent fitness contributions, which drive the photoprotein's lateral acquisition and retention, but co
49 rom re-binding of fresh chromophore to spent photoprotein, suggesting that a minority fraction of the
51 e members of a subfamily of Ca(2+)-regulated photoproteins that is a part of the larger EF-hand calci