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- W2013183862 abstract "Glucose transport has been studied in preparations of human erythrocyte ghosts which have been treated with trypsin (10μg/ml for 30 min). [3H]d-Glucose uptake by this preparation has been measured using a Millipore filter technique, with [14C]l-glucose serving as a marker for non-specific glucose uptake. Membrane vesicles prepared from erythrocyte ghosts did not preferentially take upd-glucose without prior treatment with trypsin. This trypsin-treated erythrocyte ghost preparation demonstrates many of the characteristics of glucose transport: (1) thed-isomer is both taken up and released more rapidly than thel-isomer; (2) countertransport ofd-glucose can be demonstrated; (3) competitive inhibition ofd-glucose uptake is observed with certain sugars; (4) known inhibitors of glucose uptake, phlorizin andN-ethylmaleimide, inhibitd-glucose uptake. Using very low concentrations of trypsin (1 μg/ml), the onset of glucose transport has been correlated with the pattern of cleavage of membrane peptides (assessed by polyacrylamide gel electrophoresis in sodium dodecyl sulfate). The appearance of glucose transport is temporally associated with the hydrolysis of two major membrane peptides. Specificd-glucose uptake is not inhibited by extensive proteolysis (trypsin, 100 μg/ml) or selective elution of specific peptides (by manipulation of ionic strength)." @default.
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- W2013183862 modified "2023-10-14" @default.
- W2013183862 title "Glucose transport by trypsin-treated red blood cell ghosts" @default.
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- W2013183862 doi "https://doi.org/10.1016/0005-2736(73)90502-6" @default.
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