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dc.contributor.authorIngalls, H. M.
dc.contributor.authorGoodloe-Holland, C. M.
dc.contributor.authorLuna, Elizabeth J.
dc.date2022-08-11T08:11:04.000
dc.date.accessioned2022-08-23T17:31:32Z
dc.date.available2022-08-23T17:31:32Z
dc.date.issued1986-07-01
dc.date.submitted2007-11-13
dc.identifier.citation<p>Proc Natl Acad Sci U S A. 1986 Jul;83(13):4779-83.</p>
dc.identifier.issn0027-8424 (Print)
dc.identifier.doi10.1073/pnas.83.13.4779
dc.identifier.pmid3460072
dc.identifier.urihttp://hdl.handle.net/20.500.14038/50756
dc.description.abstractRegions of plasma membrane involved in Dictyostelium discoideum intercellular adhesion resist solubilization with the nonionic detergent Triton X-100. Electron microscopy shows that these regions of the plasma membrane adhere to each other, forming many bi- and multilamellar structures. NaDodSO4/polyacrylamide gels of these regions contain major polypeptides at 225 kDa (residual myosin), 105 kDa, 88 kDa, 84 kDa, 47 kDa (residual actin), and 34 kDa. These membranes contain a subset of the total plasma membrane proteins, as analyzed by labeling of electrophoretically fractionated and blotted membrane proteins with radioiodinated Con A and by electrophoresis of membrane proteins from surface-labeled cells. Antibodies specific for gp80, a glycoprotein implicated in intercellular adhesion, intensely stain the 88-kDa and 84-kDa bands. Since these membrane regions resist Triton extraction, they appear to be stabilized by protein-protein interactions. Such stabilizing interactions may involve multivalent linkages with adjacent cells, or associations with intracellular actin and myosin, or both. Since these membranes appear to represent regions of intercellular contact, we call them "contact regions."
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3460072&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC323825/
dc.subjectAnimals
dc.subjectCell Adhesion
dc.subject*Cell Aggregation
dc.subjectCell Fractionation
dc.subjectCell Membrane
dc.subjectDictyostelium
dc.subjectMembrane Proteins
dc.subjectMicroscopy, Electron
dc.subjectMolecular Weight
dc.subjectCell Biology
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleJunctional plasma membrane domains isolated from aggregating Dictyostelium discoideum amebae
dc.typeJournal Article
dc.source.journaltitleProceedings of the National Academy of Sciences of the United States of America
dc.source.volume83
dc.source.issue13
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/wfc_pp/284
dc.identifier.contextkey392368
html.description.abstract<p>Regions of plasma membrane involved in Dictyostelium discoideum intercellular adhesion resist solubilization with the nonionic detergent Triton X-100. Electron microscopy shows that these regions of the plasma membrane adhere to each other, forming many bi- and multilamellar structures. NaDodSO4/polyacrylamide gels of these regions contain major polypeptides at 225 kDa (residual myosin), 105 kDa, 88 kDa, 84 kDa, 47 kDa (residual actin), and 34 kDa. These membranes contain a subset of the total plasma membrane proteins, as analyzed by labeling of electrophoretically fractionated and blotted membrane proteins with radioiodinated Con A and by electrophoresis of membrane proteins from surface-labeled cells. Antibodies specific for gp80, a glycoprotein implicated in intercellular adhesion, intensely stain the 88-kDa and 84-kDa bands. Since these membrane regions resist Triton extraction, they appear to be stabilized by protein-protein interactions. Such stabilizing interactions may involve multivalent linkages with adjacent cells, or associations with intracellular actin and myosin, or both. Since these membranes appear to represent regions of intercellular contact, we call them "contact regions."</p>
dc.identifier.submissionpathwfc_pp/284
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages4779-83


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