ArticleThe Journal of cell biology1985
An integral glycoprotein associated with the membrane attachment sites of actin microfilaments.
Article in The Journal of cell biology, 1985. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 63 citations in OpenAlex.
- The specific interaction of helper T cells and antigen-presenting B cells. IV. Membrane and cytoskeletal reorganizations in the bound T cell as a function of antigen dose.The Journal of experimental medicine · 1989Article
- Organisation and assembly of the surface membrane during early cleavage of the mouse embryo.Roux's archives of developmental biology : the official organ of the EDBO · 1989Article
- RGD-containing peptides inhibit the synthesis of myelin-like membrane by cultured oligodendrocytes.The Journal of cell biology · 1988Article
- An integral membrane protein antigen associated with the membrane attachment sites of actin microfilaments is identified as an integrin beta-chain.Molecular and cellular biology · 1988Article
- Dynamic membrane-cytoskeletal interactions: specific association of integrin and talin arises in vivo after phorbol ester treatment of peripheral blood lymphocytes.Proceedings of the National Academy of Sciences of the United States of America · 1988Article
- A plasma membrane integral sialoglycoprotein (Sgp 130) molecularly distinguishes nonjunctional dense plaque sites of microfilament attachment.The Journal of cell biology · 1987Article
- Interaction of the cytoskeleton with the plasma membrane.The Journal of membrane biology · 1987Review
- Regulation of fibronectin receptor distribution by transformation, exogenous fibronectin, and synthetic peptides.The Journal of cell biology · 1986Article
- Identification of a new protein localized at sites of cell-substrate adhesion.The Journal of cell biology · 1986Article
- Coupled expression and colocalization of 140K cell adhesion molecules, fibronectin, and laminin during morphogenesis and cytodifferentiation of chick lung cells.The Journal of cell biology · 1986Article
- Vinculin interaction with permeabilized cells: disruption and reconstitution of a binding site.The Journal of cell biology · 1986Article
- Relationship between the organization of actin bundles and vinculin plaques.Cell and tissue research · 1986Article
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
An integral membrane protein associated with sites of microfilament-membrane attachment has been identified by a newly developed IgG1 monoclonal antibody. This antibody, MAb 30B6, was derived from hybridoma fusion experiments using intact mitotic cells of chick embryo fibroblasts as the immunization vehicle as well as the screening probe for cell surface antigens. In immunofluorescent experiments with fixed cells, MAb 30B6 surface labeling is uniquely correlated with microfilament distributions in the cleavage furrow region of dividing chick embryo fibroblasts and cardiac myocytes in culture. The MAb 30B6 antigen in addition is associated with microfilament-membrane attachment sites in interphase fibroblasts at the dorsal surface, the adhesion plaque region at the ventral surface, and at junction-like regions of cell-cell contact. It is also found co-localized with the membrane-dense plaques of smooth muscle. The MAb 30B6 antigen is expressed in a wide number of chicken cell types (particularly smooth muscle cells, platelets, and endothelial cells), but not in erythrocytes. Some of the molecular characteristics of the MAb 30B6 antigen have been determined from immunoblotting, immunoaffinity chromatography, immunoprecipitation, cell extraction, and charge shift electrophoresis experiments. It is an integral sialoglycoprotein with an apparent molecular mass of 130 kD (reduced form)/107 kD (nonreduced form) in SDS PAGE. Another prominent glycoprotein species with an apparent molecular mass of 175 kD (reduced form)/165 kD (nonreduced form) in SDS PAGE is co-isolated on MAb 30B6 affinity columns, but appears to be antigenically distinct since it is not recognized by MAb 30B6 in immunoblotting or immunoprecipitation experiments. By virtue of its surface distributions relative to actin microfilaments and its integral protein character, we propose that the MAb 30B6 antigen is an excellent candidate for the function of directly or indirectly anchoring microfilaments to the membrane.
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