Background: The first crystal structure of the active μ opioid receptor (μOR) exhibited several unexplained features. The ligand BU72 exhibited many extreme deviations from ideal geometry, along with unexplained electron density. I previously showed that inverting the benzylic configuration resolved these problems, establishing revised stereochemistry of BU72 and its analog BU74. However, another problem remains unresolved: additional unexplained electron density contacts both BU72 and a histidine residue in the N-terminus, revealing the presence of an as-yet unidentified atom.
Results: These short contacts and uninterrupted density are inconsistent with non-covalent interactions. Therefore, BU72 and μOR form a covalent adduct, rather than representing two separate entities as in the original model. A subsequently proposed magnesium complex is inconsistent with multiple lines of evidence. However, oxygen fits the unexplained density well. While the structure I propose is tentative, similar adducts have been reported previously in the presence of reactive oxygen species. Moreover, known sources of reactive oxygen species were present: HEPES buffer, nickel ions, and a sequence motif that forms redox-active nickel complexes. This motif contacts the unexplained density. The adduct exhibits severe strain, and the tethered N-terminus forms contacts with adjacent residues. These forces, along with the nanobody used as a G protein substitute, would be expected to influence the receptor conformation. Consistent with this, the intracellular end of the structure differs markedly from subsequent structures of active μOR bound to G protein.
Conclusions: Later G-bound structures are likely to be more accurate templates for ligand docking and modelling of active G protein-bound μOR. The possibility of reactions like this should be considered in the choice of protein truncation sites and purification conditions, and in the interpretation of excess or unexplained density.
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http://dx.doi.org/10.1186/s12915-023-01689-w | DOI Listing |
Clin Nucl Med
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From the Department of Nuclear Medicine, Peking University First Hospital, Beijing.
An 18F-FDG PET/CT was conducted on a 44-year-old man with a history of dermatomyositis and avascular necrosis of left femoral head, due to a fever of unknown origin. The scan revealed patchy and cloudy high densities within the medullary cavities of bilateral distal femur and proximal tibia, exhibiting peripheral high 18F-FDG avidity. Subsequent MRI confirmed bone infarction.
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November 2024
Renji Hospital, Shanghai Jiao Tong University Medical School, Shanghai, China.
J Mol Model
November 2024
School of Agriculture, Food and Ecosystem Sciences, Faculty of Science, University of Melbourne, Royal Parade, Parkville, VIC, 3010, Australia.
To investigate the excitation mechanism of ionospheric perturbations on Mars by the Neutral Gas and Ion Mass Spectrometer (NGIMS) onboard Mars Atmosphere and Volatile EvolutioN (MAVEN), we categorize ionospheric perturbations into three cases: (a) the ion-neutral coupling cases where ion and neutral perturbations are well coupled, (b) the ion-specific cases where ion perturbations move independently from neutrals, and (c) the coronal mass ejection cases associated with solar wind extreme events. A representative number of cases from total profiles are compared with a numerical model to determine the fraction that can be explained by an atmospheric gravity waves (GW). The neutral perturbations on the dayside at 170-190 km altitudes are in excellent agreement with the GW.
View Article and Find Full Text PDFHorm Res Paediatr
November 2024
Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Introduction: Phenylketonuria (PKU), an inborn error of metabolism, when inadequately treated, may lead to nutritional deficits, which could affect bone health. This remains a controversial issue, given that in the majority of PKU cases, bone mineral density is within normal limits. On the other hand, WNT1 mutations are detrimental for bone, as they lead to primary osteoporosis.
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