FUNCTIONAL EPITOPE ANALYSIS OF THE 2ND EXTRACELLULAR LOOP OF THE HUMAN HEART MUSCARINIC ACETYLCHOLINE-RECEPTOR

被引:24
作者
FU, MLX
SCHULZE, W
WALLUKAT, G
HJALMARSON, A
HOEBEKE, J
机构
[1] GOTHENBURG UNIV, S-41345 GOTHENBURG, SWEDEN
[2] MAX DELBRUCK CTR MOLEC MED, O-1115 BERLIN, GERMANY
[3] LAB ENZYMOL & CHIM PROT, CNRS, URA 1334, F-37032 TOURS, FRANCE
关键词
ANTIBODY; CARDIOMYOCYTES; EPITOPE ANALYSIS; IMMUNOGENICITY; HEART MUSCARINIC RECEPTOR; PEPTIDE;
D O I
10.1016/S0022-2828(08)80039-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Two synthetic peptides corresponding to amino acids 172-181 and 169-193 of the second extracellular loop of the human M2 muscarinic receptor respectively were used to raise antibodies in rabbits. Affinity-purified antibodies were able not only to recognize a major band with a molecular weight of about 80 kDa on the electrotransferred membrane proteins of rat ventricular membranes but also to localize the muscarinic receptors on the sarcolemma and t-tubules of rat, cardiomyocytes. Antibodies were also able to mimic muscarinic agonist stimulation as demonstrated by a negative chronotropic effect on cultured neonatal cardiomyocytes. In contrast with the antibodies raised against the peptide 169-193, the antibodies against the peptide 172-181 were unable to inhibit muscarinic ligand binding, These results suggest that the decapeptide 172-181 contains the B-cell epitope responsible for the functional effect of antibodies directed against the second extracellular loop of the receptor. Coupling this peptide by cystein 177 blocks the induction of antibodies with pharmacological effects but induces antibodies which are able to recognize the denatured receptor protein and to exert a negative chronotropic effect.
引用
收藏
页码:427 / 436
页数:10
相关论文
共 21 条
[1]  
Bernatowicz M.S., Matsueda G.R., Preparation of peptide-protein immunogens using N-succinimidyl bromoacetate as a heterottlunctional crosslinking reagent, Anal Biochew, 155, pp. 95-102, (1986)
[2]  
Beecher M., Lewis S., Hicks J.M., Josephs S., Blocking autoantibodies in pediatric bronchial asthma, J Allergy Clin Immwiol, 74, pp. 246-251, (1984)
[3]  
Bokda E., Pascoat J., Cossio P., Dti La Vega M., Arana R., Sterin-Borda L., A circulating lg G in Chagas disease which binds to p-adrenoceptors of myocardium and modulates their activity, Clin Exp Inmnmol, 57, pp. 679-686, (1984)
[4]  
Brbndki V., Dohlman J., Blaisdel B.E., Karlin S., Very long charge runs in systemic lupus erythematosus-associated autoantigens, Proc Natl Acad Srt USA, 88, pp. 1536-1540, (1991)
[5]  
Fit L.X., Bi Ron C.H., Hoebeke J., Liang Q.M., Sjogren K.S., Waagstein F., Hjalmarson A., Effect of me-toprolol on activity of receptors coupled to G-proteins in adriamycln-induced cardiotoxlcity, Basic Res Cardio, 86, pp. 117-126, (1991)
[6]  
Fu L.X., Magnijsson Y., Berge C.H., Liljeqvtst J., Waagstein F., Hjalmarson A., Hoebeke J., Localization of autoimmune epitope on the second extracellular loop of human muscarinic receptor-2 in patients with idiopathic dilated cardiomyopathy, Jclin Invest, 91, pp. 1964-1968, (1993)
[7]  
Fu L., Hoebeke J., Magnijsson Y., Matsiji S., Matoba M., Hedner T., Herijtz H., Hjalmarson A., Autoantibodies against cardiac G-protein coupled receptors in patients with cardiomyopathy but not with hypertension, Clin Immunol Immunopalhol, 72, pp. 15-20, (1994)
[8]  
Fu L., Schulze W., Wolf W.P., Hjalmarson A., Hoebeke J., Immunocytochemical localization of M2 muscarinic receptor in rat ventricles using anti-peptide antibodies, J Histochem Cytochem, 42, pp. 337-343, (1994)
[9]  
Fu L., Wallukat G., Hjalmarson A., Hoebeke J., Agonist-like activity of anti-peptide antibodies directed against an autoimmune epitope on the heart muscarinic receptors, Receptors & Channels, 2, pp. 121-130, (1994)
[10]  
Geysen H.M., Rodda S.F., Mason G., Tribbick G., Schooes P.G., Strategies for epitope analysis using peptide synthesis, J Immunol Methods, 120, pp. 259-270, (1987)