Open Access. Powered by Scholars. Published by Universities.®
- File Type
Articles 1 - 6 of 6
Full-Text Articles in Medicine and Health Sciences
A Monomeric Protein In The Golgi Membrane Catalyzes Both N-Deacetylation And N-Sulfation Of Heparan Sulfate, Elisabet Mandon, Ellis Kempner, Masayuki Ishihara, Carlos Hirschberg
A Monomeric Protein In The Golgi Membrane Catalyzes Both N-Deacetylation And N-Sulfation Of Heparan Sulfate, Elisabet Mandon, Ellis Kempner, Masayuki Ishihara, Carlos Hirschberg
Elisabet Mandon
Recent studies have shown that the rat liver heparan sulfate N-deacetylase/N-sulfotransferase is a glycoprotein encoded by a single polypeptide chain of 882 amino acids. Using radiation inactivation analyses, we have now determined that in rat liver Golgi vesicles the target size for the N-deacetylase is 88 +/- 14 kDa, whereas that of the N-sulfotransferase is 92 +/- 8 kDa. These results, together with previous biochemical and molecular cloning approaches, demonstrate that 1) in rat liver Golgi membranes there exists only on population of molecules expressing both activities, 2) the active protein in the Golgi membrane functions as a monomer, and …
Purification Of The Golgi Adenosine 3'-Phosphate 5'-Phosphosulfate Transporter, A Homodimer Within The Membrane, Elisabet Mandon, Marcos Milla, Ellis Kempner, Carlos Hirschberg
Purification Of The Golgi Adenosine 3'-Phosphate 5'-Phosphosulfate Transporter, A Homodimer Within The Membrane, Elisabet Mandon, Marcos Milla, Ellis Kempner, Carlos Hirschberg
Elisabet Mandon
Sulfation of proteoglycans, secretory and membrane proteins, and glycolipids occurs in the lumen of the Golgi apparatus. Adenosine 3'-phosphate 5'-phosphosulfate (PAPS), the sulfate donor in these reactions, must be transported from the cytosol, its site of synthesis, into the lumen of the Golgi apparatus. We have identified and purified to apparent homogeneity the rat liver Golgi membrane PAPS transporter by a combination of conventional and affinity chromatography as well as photoaffinity radiolabeling with adenosine 3',5'-bisphosphate, a competitive inhibitor of PAPS transport. The transporter, a 75-kDa protein, was purified 70,000-fold over homogenate (6% yield) and transported PAPS into phosphatidylcholine liposomes selectively …
Synthesis And Processing Of The Alpha Heavy Chains Of Secreted And Membrane-Bound Iga, H. Kikutani, R. Sitia, R. A. Good, Janet Stavnezer
Synthesis And Processing Of The Alpha Heavy Chains Of Secreted And Membrane-Bound Iga, H. Kikutani, R. Sitia, R. A. Good, Janet Stavnezer
Janet M. Stavnezer
We have compared the synthesis and processing of immunoglobulin alpha chains in two murine cell lines, a B cell lymphoma that expresses membrane-bound IgA and a hybridoma that secretes IgA. Results of biosynthetic labeling experiments demonstrated that membrane-bound and secreted alpha chains have two distinct intracellular precursors, of different molecular weights and isoelectric points. RNAs from both of these cell lines direct the synthesis in vitro of two alpha polypeptides of Mr 59,000 and 62,000, the larger one being the precursor for membrane-bound alpha chain and the smaller one being the precursor for secreted alpha chain. These cell lines each …
A Membrane Cytoskeleton From Dictyostelium Discoideum. Ii. Integral Proteins Mediate The Binding Of Plasma Membranes To F-Actin Affinity Beads, Elizabeth J. Luna, C. M. Goodloe-Holland, H. M. Ingalls
A Membrane Cytoskeleton From Dictyostelium Discoideum. Ii. Integral Proteins Mediate The Binding Of Plasma Membranes To F-Actin Affinity Beads, Elizabeth J. Luna, C. M. Goodloe-Holland, H. M. Ingalls
Elizabeth J. Luna
In novel, low-speed sedimentation assays, highly purified, sonicated Dictyostelium discoideum plasma membrane fragments bind to F-actin beads (fluorescein-labeled F-actin on antifluorescein IgG-Sephacryl S-1000 beads). Binding was found to be (a) specific, since beads containing bound fluorescein-labeled ovalbumin or beads without bound fluorescein-labeled protein do not bind membranes, (b) saturable at approximately 0.6 microgram of membrane protein per microgram of bead-bound F-actin, (c) rapid with a t1/2 of 4-20 min, and (d) apparently of reasonable affinity since the off rate is too slow to be measured by present techniques. Using low-speed sedimentation assays, we found that sonicated plasma membrane fragments, after …
Identification By Peptide Analysis Of The Spectrin-Binding Protein In Human Erythrocytes, Elizabeth Luna, G. Kidd, D. Branton
Identification By Peptide Analysis Of The Spectrin-Binding Protein In Human Erythrocytes, Elizabeth Luna, G. Kidd, D. Branton
Elizabeth J. Luna
One-dimensional and two-dimensional peptide-mapping techniques are used to identify the protein which gives rise to the 72,000 dalton alpha-chymotryptic fragment previously shown to be the membrane attachment site for spectrin. Peptide maps of the 72,000 dalton fragment are very different from maps of Bands 1, 2, 2.9, 3, 3.1, 4.1, and 4.2 and very similar to maps of the apparently closely homologous polypeptides, Bands 2.1, 2.2, 2.3, and 2.6. Limited proteolysis of erythrocyte membranes is shown to generate Band 3', another polypeptide which has been associated with spectrin-binding activity. Peptide maps of Band 3' are very similar to maps of …
F-Actin Binds To The Cytoplasmic Surface Of Ponticulin, A 17-Kd Integral Glycoprotein From Dictyostelium Discoideum Plasma Membranes, L. J. Wuestehube, Elizabeth J. Luna
F-Actin Binds To The Cytoplasmic Surface Of Ponticulin, A 17-Kd Integral Glycoprotein From Dictyostelium Discoideum Plasma Membranes, L. J. Wuestehube, Elizabeth J. Luna
Elizabeth J. Luna
F-actin affinity chromatography and immunological techniques are used to identify actin-binding proteins in purified Dictyostelium discoideum plasma membranes. A 17-kD integral glycoprotein (gp17) consistently elutes from F-actin columns as the major actin-binding protein under a variety of experimental conditions. The actin-binding activity of gp17 is identical to that of intact plasma membranes: it resists extraction with 0.1 N NaOH, 1 mM dithiothreitol (DTT); it is sensitive to ionic conditions; it is stable over a wide range of pH; and it is eliminated by proteolysis, denaturation with heat, or treatment with DTT and N-ethylmaleimide. gp17 may be responsible for much of …