Home LiteratureArticle Details
PMID: 1380092 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Localization of epitopes for antibodies that differentially label sodium sodium channels in skeletal muscle surface and T-tubular membranes.

The Journal of membrane biology ·Vol. 128 ·No. 3 ·1992-06-00 ·Pages 219-26

Cohen SA, Barchi RL

Abstract

We previously characterized two monoclonal antibodies, A/B2 and L/D3, that bind to the amino-terminus of the sodium channel but produce distinct immunocytochemical patterns in innervated adult skeletal muscle. Because these findings suggested the presence of several channel isoforms, we sought to define the epitopes for each antibody. Five peptides encompassing the amino-terminal 126 residues of the adult skeletal muscle sodium channel were synthesized and tested by radioimmunoassay against each antibody. Both monoclonals bound only to a peptide comprising residues 1-30 (I1-30). A nested set of peptides within this region was then synthesized and used to compete for antibody binding to I1-30. L/D3 binding was quantitatively inhibited by oligopeptides 1-30, 7-30, 13-30, and 19-30 but not 25-30, while binding of A/B2 was blocked only by the intact I1-30 peptide. This data implies that the epitope for L/D3 lies within residues 19-25 while the epitope for A/B2 is contained within residues 1-6. These tentative epitope localizations were confirmed using both proteolytic cleavage of I1-30 and immunoreactivity of a peptide corresponding to residues 1-12 with A/B2 but not L/D3. Therefore, epitopes for each monoclonal antibody are present in the SkM-1 sequence and are in close proximity in the amino-terminus of the protein. Their characteristic immunocytochemical labeling patterns may reflect differing accessibility of the epitopes in various membrane environments.

MeSH Terms
Amino Acid Sequence Animals Antibodies, Monoclonal/immunology Binding, Competitive Cell Membrane/immunology Epitopes/immunology Microbial Collagenase Molecular Sequence Data Muscles/immunology,ultrastructure Rats Sodium Channels/immunology Trypsin
Chemicals
Antibodies, Monoclonal Epitopes Sodium Channels Trypsin Microbial Collagenase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cohen S A
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
Barchi R L
References (31)
31 references, click to expand
  1. New observations on the substrate specificity of cathepsin C (dipeptidyl aminopeptidase I). Including the degradation of beta-corticotropin and other peptide hormones.
    J Biol Chem. 1969 May 25;244(10):2693-709 PMID: 4306035
  2. Monoclonal antibodies against the voltage-sensitive sodium channel from rat skeletal muscle: mapping antibody binding sites.
    J Neurochem. 1987 Mar;48(3):773-8 PMID: 2433396
  3. Purification and functional reconstitution of the voltage-sensitive sodium channel from rabbit T-tubular membranes.
    J Biol Chem. 1985 May 25;260(10):6341-7 PMID: 2581954
  4. Primary structure and functional expression of a mammalian skeletal muscle sodium channel.
    Neuron. 1989 Jul;3(1):33-49 PMID: 2559760
  5. Distribution and lateral mobility of voltage-dependent sodium channels in neurons.
    J Cell Biol. 1988 Jun;106(6):1911-25 PMID: 2454930
  6. Existence of distinct sodium channel messenger RNAs in rat brain.
    Nature. 1986 Mar 13-19;320(6058):188-92 PMID: 3754035
  7. Ionic channels and their regulation by G protein subunits.
    Annu Rev Physiol. 1990;52:197-213 PMID: 1691904
  8. Analysis of protease-sensitive regions in the skeletal muscle sodium channel in vitro and implications for channel tertiary structure.
    J Biol Chem. 1991 Mar 5;266(7):4574-80 PMID: 1847924
  9. Beta-adrenergic inhibition of cardiac sodium channels by dual G-protein pathways.
    Science. 1989 Aug 4;245(4917):516-9 PMID: 2547248
  10. The voltage-sensitive sodium channel from rabbit skeletal muscle. Chemical characterization of subunits.
    J Biol Chem. 1987 Feb 15;262(5):2298-303 PMID: 2434481
  11. Ankyrin and spectrin associate with voltage-dependent sodium channels in brain.
    Nature. 1988 May 12;333(6169):177-80 PMID: 2452986
  12. Structural inferences for the native skeletal muscle sodium channel as derived from patterns of endogenous proteolysis.
    J Biol Chem. 1989 Aug 5;264(22):13273-80 PMID: 2546950
  13. Angiotensinase activity of dipeptidyl aminopeptidase I (cathepsin C) of rat liver.
    J Biol Chem. 1974 Jan 10;249(1):234-40 PMID: 4358631
  14. Molecular analysis of the para locus, a sodium channel gene in Drosophila.
    Cell. 1989 Sep 22;58(6):1143-54 PMID: 2550145
  15. Centruroides toxin, a selective blocker of surface Na+ channels in skeletal muscle: voltage-clamp analysis and biochemical characterization of the receptor.
    Proc Natl Acad Sci U S A. 1982 Jun;79(12):3896-900 PMID: 6285366
  16. Monoclonal antibodies against the voltage-sensitive Na+ channel from mammalian skeletal muscle.
    Proc Natl Acad Sci U S A. 1984 Oct;81(19):6227-31 PMID: 6207539
  17. Genomic organization and deduced amino acid sequence of a putative sodium channel gene in Drosophila.
    Science. 1987 Aug 14;237(4816):744-9 PMID: 2441469
  18. Ion pathways in transverse tubules. Quantification of receptors in membranes isolated from frog and rabbit skeletal muscle.
    Biochim Biophys Acta. 1986 Feb 13;855(1):89-98 PMID: 3002475
  19. Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence.
    Nature. 1984 Nov 8-14;312(5990):121-7 PMID: 6209577
  20. An isoform of ankyrin is localized at nodes of Ranvier in myelinated axons of central and peripheral nerves.
    J Cell Biol. 1990 Apr;110(4):1341-52 PMID: 2139035
  21. Both sodium channel II and IIA alpha subunits are expressed in rat brain.
    Nucleic Acids Res. 1990 Oct 11;18(19):5907 PMID: 2170951
  22. Use of selective toxins to separate surface and tubular sodium currents in frog skeletal muscle fibers.
    Pflugers Arch. 1988 Jan;411(1):1-7 PMID: 2451210
  23. Primary structure of rat brain sodium channel III deduced from the cDNA sequence.
    FEBS Lett. 1988 Feb 8;228(1):187-94 PMID: 2449363
  24. Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscle.
    Neuron. 1990 Feb;4(2):233-42 PMID: 2155010
  25. Differences in the properties of Na+ channels in muscle surface and T-tubular membranes revealed by tetrodotoxin derivatives.
    Pflugers Arch. 1983 Apr;397(1):1-5 PMID: 6306551
  26. Molecular cloning of a putative tetrodotoxin-resistant rat heart Na+ channel isoform.
    Proc Natl Acad Sci U S A. 1989 Oct;86(20):8170-4 PMID: 2554302
  27. Catalytic activity and arrangement of subunit polypeptides in rat liver cytochrome c oxidase as studied by proteolysis.
    Biochim Biophys Acta. 1980 Feb 8;589(2):336-45 PMID: 6243969
  28. Tityus gamma toxin, a high affinity effector of the Na+ channel in muscle, with a selectivity for channels in the surface membrane.
    Pflugers Arch. 1984 Jan;400(1):22-7 PMID: 6324066
  29. Immunoaffinity isolation of Na+ channels from rat skeletal muscle. Analysis of subunits.
    J Biol Chem. 1986 Mar 25;261(9):4318-23 PMID: 2419342
  30. Phosphorylation of the rat skeletal muscle sodium channel by cyclic AMP-dependent protein kinase.
    J Neurochem. 1990 Mar;54(3):954-62 PMID: 2154554
  31. Localization of sodium channel subtypes in adult rat skeletal muscle using channel-specific monoclonal antibodies.
    J Neurosci. 1987 Sep;7(9):2957-66 PMID: 2442326
Article Info
Journal
The Journal of membrane biology
Abbr.
J Membr Biol
ISSN
0022-2631
Published
1992-06-00
Pages
219-26
Language
English
Region
United States
NLM ID
0211301
Subset
IM
Grants
NINDS NIH HHS · NS 18013 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]