Abstract
The portion of the mannose 6-phosphate receptor (nominal Mr 180000 under nonreducing conditions) protruding at the external side of the plasma membrane of fibroblasts and HepG2 cells is susceptible to trypsin. A series of membrane-bound fragments smaller in Mr by 20000-65000 is obtained after incubation of cells with trypsin. When membranes from fibroblasts and HepG2 cells are incubated with trypsin or Staphylococcus aureus proteinase, the receptor is degraded to a single membrane-bound product smaller in Mr by about 9000. In the presence of 0.1% Triton X-100 extensive degradation of the receptor by trypsin is observed. Furthermore, the receptor in isolated membranes is sensitive to carboxypeptidase Y, which causes a decrease in Mr by about 5000 and 9000 in the absence or presence of detergent, respectively. Mannose 6-phosphate receptor appears to be a transmembrane protein with multiple trypsin-sensitive sites within its larger external (luminal) and smaller C-terminal (cytosolic) portions of the molecule.
MeSH Terms
Animals
Carboxypeptidases/pharmacology
Carrier Proteins/immunology,metabolism,pharmacology
Cell Line
Chemical Precipitation
Cytosol/metabolism
Endopeptidases/pharmacology
Fibroblasts/metabolism
Humans
Liver Neoplasms, Experimental/metabolism
Membrane Proteins/metabolism
Receptor, IGF Type 2
Serine Endopeptidases
Trypsin/pharmacology
Chemicals
Carrier Proteins
Membrane Proteins
Receptor, IGF Type 2
Carboxypeptidases
Endopeptidases
serine carboxypeptidase
Serine Endopeptidases
glutamyl endopeptidase
Trypsin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
von Figura K
Gieselmann V
Hasilik A
References (13)
13 references, click to expand
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