Improvement in the properties of 3-phenyl-3-trifluoromethyldiazirine based photoreactive bis-glucose probes for GLUT4 following substitution on the phenyl ring.

We have developed two novel 3-phenyl-3-trifluoromethyldiazirinyl bis-glucose derivatives to investigate the properties of the adipocyte glucose transporter GLUT4. These compounds were substituted by electron-withdrawing (iodo and nitro) groups on the aromatic ring of 3-phenyl-3-trifluoromethyldiazirine photophore and were found to be more photosensitive than compounds without such substituents. The compounds were used as inhibitors of insulin-stimulated glucose transport activity in order to assess half-maximal inhibition or relative affinity values for GLUT4. The affinities were found to be 60-130 times higher than the parent compound D-glucose. Because of the increased photo-reactivity and high affinity these compounds will be useful in studies directed at further elucidation of GLUT4 function.

[1]  M. Hashimoto,et al.  Versatile synthesis of phenoxydiazirine-based fatty acid analogues and photoreactive galactosylceramide. , 2002, Bioorganic & medicinal chemistry letters.

[2]  I. Sandoval,et al.  Moving the insulin-regulated glucose transporter GLUT4 into and out of storage. , 2001, Trends in cell biology.

[3]  G. Holman,et al.  Synthesis of biotinylated bis(D-glucose) derivatives for glucose transporter photoaffinity labelling. , 2001, Carbohydrate research.

[4]  H. Joost,et al.  The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members , 2001, Molecular membrane biology.

[5]  M. Hashimoto,et al.  Novel photoreactive cinnamic acid analogues to elucidate phenylalanine ammonia-lyase. , 2000, Bioorganic & medicinal chemistry letters.

[6]  J. Zierath,et al.  Use of a novel impermeable biotinylated photolabeling reagent to assess insulin- and hypoxia-stimulated cell surface GLUT4 content in skeletal muscle from type 2 diabetic patients. , 2000, Diabetes.

[7]  S. Baldwin Membrane transport : a practical approach , 2000 .

[8]  W. Rees,et al.  Synthesis of symmetrical 4,4′- and 6,6′- bis(D-glucose)-based probes as tools for the study of D-glucose transport proteins , 1999 .

[9]  M. Hashimoto,et al.  A Rapid and Efficient Method for Identifying Photoaffinity Biotinylated Sites within Proteins , 1998 .

[10]  S. Hashimoto,et al.  N-glycosylation with glycosyl diethyl phosphites: A highly stereoselective synthesis of 2′-deoxy-β-ribonucleosides , 1997 .

[11]  M. Hashimoto,et al.  A VERSATILE APPROACH FOR FUNCTIONALIZATION OF 3-ARYL-3-TRIFLUOROMETHYLDIAZIRINE PHOTOPHOR , 1997 .

[12]  M. Hashimoto,et al.  A Novel Family of Aromatic Diazirines for Photoaffinity Labeling , 1994 .

[13]  G. Gould,et al.  The glucose transporter family: structure, function and tissue-specific expression. , 1993, The Biochemical journal.

[14]  I. Simpson,et al.  Cell surface labeling of glucose transporter isoform GLUT4 by bis-mannose photolabel. Correlation with stimulation of glucose transport in rat adipose cells by insulin and phorbol ester. , 1990, The Journal of biological chemistry.

[15]  G. Holman,et al.  Photolabeling of erythrocyte and adipocyte hexose transporters using a benzophenone derivative of bis(D-mannose). , 1988, Biochimica et biophysica acta.

[16]  G. Holman,et al.  Exofacial photoaffinity labelling of the human erythrocyte sugar transporter. , 1986, Biochimica et biophysica acta.

[17]  G. Holman,et al.  Interaction of hydrophobic bis (D-mannose) derivatives with adipocyte and erythrocyte sugar transport systems. , 1985, Biochimica et biophysica acta.

[18]  W. Rees,et al.  Side-specific analogues for the rat adipocyte sugar transport system. , 1982, Biochimica et biophysica acta.

[19]  W. Rees,et al.  Hydrogen bonding requirements for the insulin-sensitive sugar transport system of rat adipocytes. , 1981, Biochimica et biophysica acta.

[20]  G. Holman,et al.  An explanation of the asymmetric binding of sugars to the human erythrocyte sugar-transport systems. , 1973, The Biochemical journal.