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1.
FEBS Lett ; 308(1): 101-5, 1992 Aug 10.
Article in English | MEDLINE | ID: mdl-1379548

ABSTRACT

Protein sequencing shows that porcine brain tubulin retains the N-terminal sequences of alpha and beta tubulin after a mild treatment with subtilisin. C-terminal peptides released by subtilisin were purified and characterized by automated Edman degradation and mass spectrometry. We confirm the polyglutamylation of alpha tubulin on glutamic acid residue 445 reported by others and show in addition that class II beta tubulin, the major beta tubulin isotype of adult brain, is also polyglutamylated. The substitution is restricted to glutamic acid residue 435. Thus all major tubulin isotypes of adult brain are subjected to polyglutamylation.


Subject(s)
Glutamates/metabolism , Polyglutamic Acid/metabolism , Tubulin/metabolism , Amino Acid Sequence , Animals , Chromatography, Liquid , Electrophoresis, Polyacrylamide Gel , Glutamic Acid , Mass Spectrometry , Molecular Sequence Data , Subtilisins/chemistry , Swine , Tubulin/genetics
2.
Am J Pathol ; 140(5): 1215-23, 1992 May.
Article in English | MEDLINE | ID: mdl-1374594

ABSTRACT

The monoclonal antibody MAb 155, isolated by Tzartos et al, recognizes the alpha subunit of acetylcholine receptor (AChR) and stains type II skeletal muscle fibers but does not decorate heart muscle. In addition it reacts with most myasthenia gravis-associated thymomas. The authors show by immunoblotting techniques that the myofibrillar antigen is a 23 kd protein and by partial protein sequence data identify it as fast troponin I. Fast troponin I from various species contains the sequence EEKSGMEGRK close to the C-terminal end at positions 165 to 174. The first lysine (K) is crucial for MAb 155 reactivity since its substitution by methionine and leucine in slow troponin I and cardiac troponin I, respectively, abolishes MAb 155 reactivity. The epitope identified on troponin I is homologous in sequence with the MAb 155 epitope on the AChR alpha subunit established by direct peptide binding as KSAIEGIK (positions 373-380). The authors consider whether fortuitously shared epitopes can be responsible for the high level of autoantibodies to AChR and to muscle proteins seen in many MG patients.


Subject(s)
Epitopes , Muscles/metabolism , Myasthenia Gravis/etiology , Receptors, Cholinergic/immunology , Troponin/immunology , Amino Acid Sequence , Animals , Antibodies, Monoclonal , Cattle , Chickens , Female , Humans , Immunoblotting , Immunohistochemistry , Mice , Molecular Sequence Data , Rats , Receptors, Cholinergic/chemistry , Species Specificity , Troponin/genetics , Troponin I
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