Literature DB >> 6885756

Characterization and localization of the Mr = 43,000 proteins associated with acetylcholine receptor-rich membranes.

S Porter, S C Froehner.   

Abstract

A protein of Mr = 43,000 (43K protein) is a major component of highly purified postsynaptic membranes isolated from Torpedo electric organ. It can be removed from these membranes by alkaline treatment or with 10 mM lithium diiodosalicylate, conditions which extract peripheral membrane proteins without solubilizing the acetylcholine receptor. Two-dimensional polyacrylamide gel electrophoresis of the lithium diiodosalicylate extract shows it to contain several major Mr = 43,000 components of isoelectric points between 7.0 and 8.0 and a minor component of approximately pI 5.6. The pI 5.6 polypeptide co-migrates with skeletal muscle actin on a two-dimensional gel and gives a peptide map pattern very similar to that of actin. The three major spots of pI 7.0-8.0 yield peptide maps which are indistinguishable from one another but quite different from that of actin. The membrane-bound forms of both the basic 43K protein and actin can be iodinated in a lactoperoxidase-catalyzed reaction only if the membrane vesicles are first permeabilized with saponin, a treatment which permits entry of macromolecules to the interior of the vesicles. An immunoblot of a two-dimensional gel shows that a rabbit antiserum made against alkaline extract reacts strongly with the basic 43K protein and to lesser extent with an acidic component of Mr = 55,000 but not with actin. Immunofluorescence studies have shown that this antiserum reacts with the innervated face of Torpedo electrocytes and recognizes a component of rat diaphragm muscle which is highly concentrated at the neuromuscular junction (Froehner, S.C., Gulbrandsen, V., Hyman, C., Jeng, A. Y., Neubig, R. R., and Cohen, J. B. (1981) Proc. Natl. Acad. Sci. U. S. A. 78, 5230-5234). Similar experiments on intact rat muscle indicate that, like the 43K protein of Torpedo postsynaptic membranes, the immunologically related component in mammalian muscle endplates is located on the cytoplasmic side of the postsynaptic membrane.

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Year:  1983        PMID: 6885756

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  28 in total

1.  The actin-driven movement and formation of acetylcholine receptor clusters.

Authors:  Z Dai; X Luo; H Xie; H B Peng
Journal:  J Cell Biol       Date:  2000-09-18       Impact factor: 10.539

2.  Transglutaminase in membranes rich in nicotinic acetylcholine receptors.

Authors:  G Bandini; F Hucho
Journal:  J Protein Chem       Date:  1989-06

3.  2-D- and 3-D-ordered structures of acetylcholine receptors.

Authors:  M Giersig; S Hertling-Jaweed; F Hucho
Journal:  J Protein Chem       Date:  1989-06

4.  Tyrosine phosphorylation of nicotinic acetylcholine receptor mediates Grb2 binding.

Authors:  M Colledge; S C Froehner
Journal:  J Neurosci       Date:  1997-07-01       Impact factor: 6.167

Review 5.  Yotiao, a novel protein of neuromuscular junction and brain that interacts with specific splice variants of NMDA receptor subunit NR1.

Authors:  J W Lin; M Wyszynski; R Madhavan; R Sealock; J U Kim; M Sheng
Journal:  J Neurosci       Date:  1998-03-15       Impact factor: 6.167

6.  The subsynaptic 43-kDa protein is concentrated at developing nerve-muscle synapses in vitro.

Authors:  S J Burden
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

7.  Cholesterol modulates the rate and mechanism of acetylcholine receptor internalization.

Authors:  Virginia Borroni; Francisco J Barrantes
Journal:  J Biol Chem       Date:  2011-02-28       Impact factor: 5.157

8.  Direct cross-linking of 125I-labeled glucagon to its membrane receptor by UV irradiation.

Authors:  V Iwanij; K C Hur
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

9.  nu 1, a Mr 43,000 component of postsynaptic membranes, is a protein kinase.

Authors:  A S Gordon; D Milfay
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

10.  The 43-K protein, v1, associated with acetylcholine receptor containing membrane fragments is an actin-binding protein.

Authors:  J H Walker; C M Boustead; V Witzemann
Journal:  EMBO J       Date:  1984-10       Impact factor: 11.598

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