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1.
Intern Med ; 55(20): 3021-3024, 2016.
Article in English | MEDLINE | ID: mdl-27746442

ABSTRACT

A 39-year-old man presented to our hospital with a four-week history of headache and a two-week history of low-grade fever. Chest X-rays showed a tumor of approximately 50 mm in size in the right lower field. A histopathological examination of a transbronchial lung biopsy specimen from the right S9/10 revealed numerous fungal elements that appeared as encapsulated yeast with clear halos. Gadolinium-enhanced brain magnetic resonance images showed multiple cerebral nodules. Cryptococcus gattii (Genotype VGIIa) was isolated from the bronchial lavage and cerebrospinal fluid specimens. The patient was an immunocompetent Japanese man who had not recently traveled to a C. gattii-endemic area.


Subject(s)
Cryptococcosis/diagnostic imaging , Cryptococcosis/microbiology , Cryptococcus gattii/isolation & purification , Adult , Humans , Japan , Magnetic Resonance Imaging , Male , Tomography, X-Ray Computed
2.
J Biochem ; 135(5): 589-96, 2004 May.
Article in English | MEDLINE | ID: mdl-15173197

ABSTRACT

We have expressed a M(2)-Galpha(i1) fusion protein in insect cells, in which the G protein alpha(i1) subunit was fused with a mutant of the muscarinic receptor M(2) subtype without glycosylation sites and the central part of the third intracellular loop. The M(2)-Galpha(i1) fusion protein showed GTP-sensitive, high-affinity agonist binding. Displacement curves by GDP of [(35)S]GTPgammaS binding shifted to the right in the presence of muscarinic agonists. The extent of the shift was greater for full agonists (120-150 fold) than for partial agonists (25-35 fold), and virtually no shift was observed for antagonists. The affinity for GDP decreased with increasing MgCl(2) concentration in the presence of an agonist but was not affected by MgCl(2) in the presence of an antagonist. These results indicate that the apparent affinity for GDP of the M(2)-Galpha(i1) fusion protein bound to a ligand represents the efficacy of the given ligand, and that Mg(2+) is required for the agonist-bound M(2) to interact with Galpha(i1), reducing its affinity for GDP. We propose that the agonist-M(2)-Galpha(i1) complex represents the transition state for the GDP-GTP exchange reaction catalyzed by agonist-bound receptors, and that the complex has different affinities for GDP depending on the species of the ligand bound to M(2) receptors.


Subject(s)
GTP-Binding Protein alpha Subunits, Gi-Go/chemistry , Magnesium/chemistry , Receptor, Muscarinic M2/chemistry , Alternative Splicing , Animals , Baculoviridae/metabolism , Biochemistry/methods , Cattle , Dose-Response Relationship, Drug , GTP-Binding Protein alpha Subunits, Gi-Go/metabolism , Guanosine Diphosphate/metabolism , Guanosine Triphosphate/metabolism , Humans , Insecta , Ions , Ligands , Magnesium Chloride/chemistry , Magnesium Chloride/metabolism , Models, Biological , Protein Binding , Protein Structure, Tertiary , Receptor, Muscarinic M2/metabolism , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/metabolism , Time Factors
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