TY - JOUR
T1 - Beetle luciferases with naturally red- and blue-shifted emission
AU - Carrasco-López, César
AU - Ferreira, Juliana C.
AU - Lui, Nathan M.
AU - Schramm, Stefan
AU - Berraud-Pache, Romain
AU - Navizet, Isabelle
AU - Panjikar, Santosh
AU - Naumov, Panče
AU - Rabeh, Wael M.
N1 - Publisher Copyright:
© 2018 Carrasco-López et al.
PY - 2018
Y1 - 2018
N2 - The different colors of light emitted by bioluminescent beetles that use an identical substrate and chemiexcitation reaction sequence to generate light remain a challenging and controversial mechanistic conundrum. The crystal structures of two beetle luciferases with red- and blue-shifted light relative to the green yellow light of the common firefly species provide direct insight into the molecular origin of the bioluminescence color. The structure of a blue-shifted green-emitting luciferase from the firefly Amydetes vivianii is monomeric with a structural fold similar to the previously reported firefly luciferases. The only known naturally red-emitting luciferase from the glow-worm Phrixothrix hirtus exists as tetramers and octamers. Structural and computational analyses reveal varying aperture between the two domains enclosing the active site. Mutagenesis analysis identified two conserved loops that contribute to the color of the emitted light. These results are expected to advance comparative computational studies into the conformational landscape of the luciferase reaction sequence.
AB - The different colors of light emitted by bioluminescent beetles that use an identical substrate and chemiexcitation reaction sequence to generate light remain a challenging and controversial mechanistic conundrum. The crystal structures of two beetle luciferases with red- and blue-shifted light relative to the green yellow light of the common firefly species provide direct insight into the molecular origin of the bioluminescence color. The structure of a blue-shifted green-emitting luciferase from the firefly Amydetes vivianii is monomeric with a structural fold similar to the previously reported firefly luciferases. The only known naturally red-emitting luciferase from the glow-worm Phrixothrix hirtus exists as tetramers and octamers. Structural and computational analyses reveal varying aperture between the two domains enclosing the active site. Mutagenesis analysis identified two conserved loops that contribute to the color of the emitted light. These results are expected to advance comparative computational studies into the conformational landscape of the luciferase reaction sequence.
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U2 - 10.26508/lsa.201800072
DO - 10.26508/lsa.201800072
M3 - Article
C2 - 30456363
AN - SCOPUS:85056991185
SN - 2575-1077
VL - 1
JO - Life science alliance
JF - Life science alliance
IS - 4
M1 - e201800072
ER -