Literature DB >> 3693407

Nerve terminal anchorage protein 1 (TAP-1) is a chondroitin sulfate proteoglycan: biochemical and electron microscopic characterization.

S S Carlson1, T N Wight.   

Abstract

The plasma membranes of the nerve terminal and the postsynaptic cell of electric organ are separated by a basal lamina. We have purified, biochemically characterized, and visualized in the electron microscope a macromolecule which appears to anchor the nerve terminal to this basal lamina. This molecule, terminal anchorage protein 1 (TAP-1) is associated with the nerve terminal membrane of electric organ, has the properties of an integral membrane protein, and is tightly bound to the extracellular matrix (Carlson, S.S., P. Caroni, and R.B. Kelly. 1986. J. Cell Biol. 103:509-520). TAP-1 can be solubilized from an electric organ extracellular matrix preparation with guanidine-HCl/3-[(3-cholamidopropyl)-dimethylammnio]-1-propane sulfonate and purified by a combination of permeation chromatography on Sephacryl S-1000, sedimentation velocity, and ion exchange chromatography on DEAE Sephacel. The total purification from electric organ is 91-fold and results in at least 86% purity. Digestion of the molecule with chondroitin ABC or AC lyase produces a large but similar shift in the molecular weight of the molecule on SDS-PAGE. The presence of chondroitin-4- or 6-sulfate is confirmed by identification of the isolated glycosaminoglycans with cellulose acetate electrophoresis. Gel filtration of the isolated chains indicates an average molecular weight of 42,000. Digestion of TAP-1 with other glycosaminoglycan lyases such as heparitinase indicates that only chondroitin sulfate is present. These results demonstrate that TAP-1 is a proteoglycan. Visualization of TAP-1 in the electron microscope reveals a "bottlebrush" structure expected for a proteoglycan. The molecule has an average total length of 345 +/- 17 nm with 20 +/- 2 side projections of 113 +/- 5 nm in length. These side projections are presumably the glycosaminoglycan side chains. From this structure, we predict that the TAP-1 glycosaminoglycan side chains should have a molecular weight of approximately 50,000, which is in close agreement with the biochemical studies. Both biochemical and morphologic data indicate that TAP-1 has a relative molecular weight of approximately 1.2 X 10(6). The large size of TAP-1 suggests that this molecule could span the synaptic cleft and make a significant contribution to the structure of the nerve terminal basal lamina of electric organ.

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Year:  1987        PMID: 3693407      PMCID: PMC2114688          DOI: 10.1083/jcb.105.6.3075

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  31 in total

1.  A rapid, sensitive, and specific method for the determination of protein in dilute solution.

Authors:  W Schaffner; C Weissmann
Journal:  Anal Biochem       Date:  1973-12       Impact factor: 3.365

2.  A method for the determination of the molecular weight and molecular-weight distribution of chondroitin sulphate.

Authors:  A Wasteson
Journal:  J Chromatogr       Date:  1971-07-08

3.  Structures and immunochemical properties of oligosaccharides isolated from pig submaxillary mucins.

Authors:  D M Carlson
Journal:  J Biol Chem       Date:  1968-02-10       Impact factor: 5.157

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  Proteinase activity in chondroitin lyase (chondroitinase) and endo-beta-D-galactosidase (keratanase) preparations and a method to abolish their proteolytic effect on proteoglycan.

Authors:  Y Oike; K Kimata; T Shinomura; S Suzuki
Journal:  Biochem J       Date:  1980-10-01       Impact factor: 3.857

6.  Cartilage proteoglycans: comparison of sectioned and spread whole molecules.

Authors:  G K Hascall
Journal:  J Ultrastruct Res       Date:  1980-03

7.  Cell-surface heparan sulfate: an intercalated membrane proteoglycan.

Authors:  L Kjellén; I Pettersson; M Höök
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

8.  Isolation of glycosaminoglycans (heparan sulfate) from glomerular basement membranes.

Authors:  Y S Kanwar; M G Farquhar
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

9.  Synaptic vesicles in electromotoneurones. II. Heterogeneity of populations is expressed in uptake properties; exocytosis and insertion of a core proteoglycan into the extracellular matrix.

Authors:  H Stadler; M L Kiene
Journal:  EMBO J       Date:  1987-08       Impact factor: 11.598

10.  Reinnervation of muscle fiber basal lamina after removal of myofibers. Differentiation of regenerating axons at original synaptic sites.

Authors:  J R Sanes; L M Marshall; U J McMahan
Journal:  J Cell Biol       Date:  1978-07       Impact factor: 10.539

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  7 in total

Review 1.  Extracellular matrix molecules and their receptors: functions in neural development.

Authors:  L F Reichardt; K J Tomaselli
Journal:  Annu Rev Neurosci       Date:  1991       Impact factor: 12.449

Review 2.  The cell biology of the nerve terminal.

Authors:  R B Kelly
Journal:  Neuron       Date:  1988-08       Impact factor: 17.173

Review 3.  Isolation and purification of proteoglycans.

Authors:  N S Fedarko
Journal:  Experientia       Date:  1993-05-15

Review 4.  Proteoglycans and the acute-phase response in Alzheimer's disease brain.

Authors:  B Leveugle; H Fillit
Journal:  Mol Neurobiol       Date:  1994 Aug-Dec       Impact factor: 5.590

5.  Heparin modulates the composition of the extracellular matrix domain surrounding arterial smooth muscle cells.

Authors:  A D Snow; R P Bolender; T N Wight; A W Clowes
Journal:  Am J Pathol       Date:  1990-08       Impact factor: 4.307

6.  Membrane-associated chondroitin sulfate proteoglycans of human lung fibroblasts.

Authors:  G David; V Lories; A Heremans; B Van der Schueren; J J Cassiman; H Van den Berghe
Journal:  J Cell Biol       Date:  1989-03       Impact factor: 10.539

7.  Tyrosine phosphorylation and acetylcholine receptor cluster formation in cultured Xenopus muscle cells.

Authors:  L P Baker; H B Peng
Journal:  J Cell Biol       Date:  1993-01       Impact factor: 10.539

  7 in total

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