Localization of the forskolin photolabelling site within the monosaccharide transporter of human erythrocytes.

Wadzinski BE, Shanahan MF, Seamon KB, Ruoho AE
Biochem J. 1990 272 (1): 151-8

PMID: 2264820 · PMCID: PMC1149670 · DOI:10.1042/bj2720151

Chemical and proteolytic digestion of intact erythrocyte glucose transporter as well as purified transporter protein has been used to localize the derivatization site for the photoaffinity agent 3-[125I]iodo-4-azido-phenethylamino-7-O-succinyldeacetylforskol in [( 125I]IAPS-forskolin). Comparison of the partial amino acid sequence of the labelled 18 kDa tryptic fragment with the known amino acid sequence for the HepG2 glucose transporter confirmed that the binding site for IAPS-forskolin is between the amino acid residues Glu254 and Tyr456. Digestion of intact glucose transporter with Pronase suggests that this site is within the membrane bilayer. Digestion of labelled transporter with CNBr generated a major radiolabelled fragment of Mr approximately 5800 putatively identified as residues 365-420. Isoelectric focusing of Staphylococcus aureus V8 proteinase-treated purified labelled tryptic fragment identified two peptides which likely correspond to amino acid residues 360-380 and 381-393. The common region for these radiolabelled peptides is the tenth putative transmembrane helix of the erythrocyte glucose transporter, comprising amino acid residues 369-389. Additional support for this conclusion comes from studies in which [125I]APS-forskolin was photoincorporated into the L-arabinose/H(+)-transport protein of Escherichia coli. Labelling of this transport protein was protected by both cytochalasin B and D-glucose. The region of the erythrocyte glucose transporter thought to be derivatized with IAPS-forskolin contains a tryptophan residue (Trp388) that is conserved in the sequence of the E. coli arabinose-transport protein.

MeSH Terms (15)

Affinity Labels Amino Acid Sequence Azides Binding Sites Colforsin Cytochalasin B Diterpenes Electrophoresis, Polyacrylamide Gel Erythrocyte Membrane Models, Molecular Molecular Sequence Data Molecular Weight Monosaccharide Transport Proteins Peptide Fragments Protein Conformation

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