TY - JOUR
T1 - Mutations in human dynamin block an intermediate stage in coated vesicle formation
AU - Van Der Bliek, Alexander M.
AU - Redelmeier, Thomas E.
AU - Damke, Hanna
AU - Tisdale, Ellen J.
AU - Meyerowitz, Elliot M.
AU - Schmid, Sandra L.
PY - 1993
Y1 - 1993
N2 - The role of human dynamin in receptor-mediated endocytosis was investigated by transient expression of GTP-binding domain mutants in mammalian cells. Using assays which detect intermediates in coated vesicle formation, the dynamin mutants were found to block endocytosis at a stage after the initiation of coat assembly and preceding the sequestration of ligands into deeply invaginated coated pits. Membrane transport from the ER to the Golgi complex was unaffected indicating that dynamin mutants specifically block early events in endocytosis. These results demonstrate that mutations in the GTP-binding domain of dynamin block Tfn-endocytosis in mammalian cells and suggest that a functional dynamin GTPase is required for receptor-mediated endocytosis via clathrin-coated pits.
AB - The role of human dynamin in receptor-mediated endocytosis was investigated by transient expression of GTP-binding domain mutants in mammalian cells. Using assays which detect intermediates in coated vesicle formation, the dynamin mutants were found to block endocytosis at a stage after the initiation of coat assembly and preceding the sequestration of ligands into deeply invaginated coated pits. Membrane transport from the ER to the Golgi complex was unaffected indicating that dynamin mutants specifically block early events in endocytosis. These results demonstrate that mutations in the GTP-binding domain of dynamin block Tfn-endocytosis in mammalian cells and suggest that a functional dynamin GTPase is required for receptor-mediated endocytosis via clathrin-coated pits.
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U2 - 10.1083/jcb.122.3.553
DO - 10.1083/jcb.122.3.553
M3 - Article
C2 - 8101525
AN - SCOPUS:0027203046
SN - 0021-9525
VL - 122
SP - 553
EP - 563
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 3
ER -