Identification of two lysosomal membrane glycoproteins.
Open Access
- 1 July 1985
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 101 (1), 85-95
- https://doi.org/10.1083/jcb.101.1.85
Abstract
Two murine lysosome-associated membrane proteins, LAMP-1 of 105,000-115,000 D and LAMP-2 of 100,000-110,000 D, have been identified by monoclonal antibodies that bind specifically to lysosomal membranes. Both glycoproteins were distinguished as integral membrane components solubilized by detergent solutions but not by various chaotropic agents. The lysosome localization was demonstrated by indirect immunofluorescent staining, co-localization of the antigen to sites of acridine orange uptake, and immunoelectron microscopy. Antibody binding was predominantly located at the limiting lysosomal membrane, distinctly separated from colloidal gold-labeled alpha-2-macroglobulin accumulated in the lumen during prolonged incubation. LAMP-1 and LAMP-2 also appeared to be present in low concentrations on Golgi trans-elements but were not detected in receptosomes marked by the presence of newly endocytosed alpha-2-macroglobulin, or in other cellular structures. LAMP-1 and LAMP-2 were distinguished as different molecules by two-dimensional gel analysis, 125I-tryptic peptide mapping, and sequential immunoprecipitations of 125I-labeled cell extracts. Both glycoproteins were synthesized as a precursor protein of approximately 90,000 D, and showed a marked heterogeneity of apparent molecular weight expression in different cell lines. LAMP-2 was closely related or identical to the macrophage antigen, MAC-3, as indicated by antibody adsorption and tryptic peptide mapping. It is postulated that these glycoproteins, as major protein constituents of the lysosomal membrane, have important roles in lysosomal structure and function.This publication has 27 references indexed in Scilit:
- Antibodies against lysosomal membranes reveal a 100,000-mol-wt protein that cross-reacts with purified H+,K+ ATPase from gastric mucosa.The Journal of cell biology, 1984
- Fusion of intracellular membrane pools with cell surfaces of macrophages stimulated by phorbol esters and calcium ionophoresCell, 1984
- Lysosomes revisitedEuropean Journal of Biochemistry, 1983
- Membrane proteins of the vacuolar system. III. Further studies on the composition and recycling of endocytic vacuole membrane in cultured macrophagesThe Journal of cell biology, 1983
- Antibodies to the Golgi complex and the rough endoplasmic reticulum.The Journal of cell biology, 1982
- A monoclonal antibody that recognizes Golgi-associated protein of cultured fibroblast cells.The Journal of cell biology, 1982
- alpha 2-macroglobulin adsorbed to colloidal gold: a new probe in the study of receptor-mediated endocytosis.The Journal of cell biology, 1981
- Stabilization of proteins immobilized on Sepharose from leakage by glutaraldehyde crosslinkingAnalytical Biochemistry, 1980
- Localization of serum-derived α2 macroglobulin in cultured cells and decrease after moloney sarcoma virus transformationCell, 1977
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970