TY - JOUR
T1 - Ligand pathways in neuroglobin revealed by low-temperature photodissociation and docking experiments
AU - Ardiccioni, Chiara
AU - Arcovito, Alessandro
AU - Longa, Stefano Della
AU - Van Der Linden, Peter
AU - Bourgeois, Dominique
AU - Weik, Martin
AU - Montemiglio, Linda Celeste
AU - Savino, Carmelinda
AU - Avell, Giovanna
AU - Exertier, Cécile
AU - Carpentier, Philippe
AU - Prangé, Thierry
AU - Brunori, Maurizio
AU - Colloc'H, Nathalie
AU - Vallone, Beatrice
PY - 2019
Y1 - 2019
N2 - A combined biophysical approach was applied to map gas-docking sites within murine neuroglobin (Ngb), revealing snapshots of events that might govern activity and dynamics in this unique hexacoordinate globin, which is most likely to be involved in gas-sensing in the central nervous system and for which a precise mechanism of action remains to be elucidated. The application of UV-visible microspectroscopy in crystallo, solution X-ray absorption near-edge spectroscopy and X-ray diffraction experiments at 15-40 K provided the structural characterization of an Ngb photolytic intermediate by cryo-trapping and allowed direct observation of the relocation of carbon monoxide within the distal heme pocket after photodissociation. Moreover, X-ray diffraction at 100 K under a high pressure of dioxygen, a physiological ligand of Ngb, unravelled the existence of a storage site for O2 in Ngb which coincides with Xe-III, a previously described docking site for xenon or krypton. Notably, no other secondary sites were observed under our experimental conditions.
AB - A combined biophysical approach was applied to map gas-docking sites within murine neuroglobin (Ngb), revealing snapshots of events that might govern activity and dynamics in this unique hexacoordinate globin, which is most likely to be involved in gas-sensing in the central nervous system and for which a precise mechanism of action remains to be elucidated. The application of UV-visible microspectroscopy in crystallo, solution X-ray absorption near-edge spectroscopy and X-ray diffraction experiments at 15-40 K provided the structural characterization of an Ngb photolytic intermediate by cryo-trapping and allowed direct observation of the relocation of carbon monoxide within the distal heme pocket after photodissociation. Moreover, X-ray diffraction at 100 K under a high pressure of dioxygen, a physiological ligand of Ngb, unravelled the existence of a storage site for O2 in Ngb which coincides with Xe-III, a previously described docking site for xenon or krypton. Notably, no other secondary sites were observed under our experimental conditions.
KW - CO photolysis
KW - XANES
KW - cryo-trapping
KW - crystal microspectroscopy
KW - heme protein
KW - neuroglobin
KW - neuroprotection
KW - oxygen binding
KW - protein structure
KW - soak-and-freeze pressurization
KW - structural biology
KW - structure determination
KW - ultralow-temperature X-ray crystallography
KW - CO photolysis
KW - XANES
KW - cryo-trapping
KW - crystal microspectroscopy
KW - heme protein
KW - neuroglobin
KW - neuroprotection
KW - oxygen binding
KW - protein structure
KW - soak-and-freeze pressurization
KW - structural biology
KW - structure determination
KW - ultralow-temperature X-ray crystallography
UR - http://hdl.handle.net/10807/147475
UR - http://www.iucrj.org/m/
U2 - 10.1107/S2052252519008157
DO - 10.1107/S2052252519008157
M3 - Article
SN - 2052-2525
VL - 6
SP - 832
EP - 842
JO - IUCrJ
JF - IUCrJ
ER -