Literature DB >> 1706314

Monoclonal antibodies against cardiac myosin heavy chain.

J P Jin1, M L Malik, J J Lin.   

Abstract

Three mouse IgG1 monoclonal antibodies (MAbs), named FA1, FA2, and FA3, against cardiac myosin heavy chain (MHC) with high specificity have been obtained. The immunogen used to generate these MAbs was the high-salt- and detergent-insoluble fraction of adult rat myocardial tissue. Western blots showed that these MAbs reacted with a 200 kD protein band, which comigrated with the heavy chain of purified rat cardiac myosin in SDS-PAGE. Immunofluorescence microscopy revealed that the antigen recognized by these MAbs was localized at the A-band of isolated myofibrils. The tissue-, species-, and isoform-specificities of these MAbs were examined by Western blots on various muscle samples. FA2 recognized fish, frog, chicken, rabbit, bovine, mouse and rat cardiac MHC, as well as rabbit skeletal and rat aorta smooth muscle MHC. This antibody reacted equally well with both alpha- and beta-isoforms of MHC. FA1 did not crossreact with any MHC tested so far but with rat cardiac MHC. It appeared to react only with alpha-isoform of MHC. FA3 recognized only rat, bovine and rabbit cardiac MHC with the specificity to bovine and rabbit atrial MHC. Elisa competition assay revealed that different epitopes on the antigen molecules were recognized by these three MAbs, although there was a partial overlap between the epitopes for FA1 and FA2. These anti-MHC MAbs will be most useful in investigating the expression of MHC during myocardial development.

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Year:  1990        PMID: 1706314     DOI: 10.1089/hyb.1990.9.597

Source DB:  PubMed          Journal:  Hybridoma        ISSN: 0272-457X


  16 in total

1.  Toad heart utilizes exclusively slow skeletal muscle troponin T: an evolutionary adaptation with potential functional benefits.

Authors:  Han-Zhong Feng; Xuequn Chen; M Moazzem Hossain; Jian-Ping Jin
Journal:  J Biol Chem       Date:  2012-07-09       Impact factor: 5.157

2.  Slow recovery of the impaired fatigue resistance in postunloading mouse soleus muscle corresponding to decreased mitochondrial function and a compensatory increase in type I slow fibers.

Authors:  Han-Zhong Feng; Xuequn Chen; Moh H Malek; J-P Jin
Journal:  Am J Physiol Cell Physiol       Date:  2015-10-07       Impact factor: 4.249

3.  Rats genetically selected for low and high aerobic capacity exhibit altered soleus muscle myofilament functions.

Authors:  B J Biesiadecki; M A Brotto; L S Brotto; L G Koch; S L Britton; T M Nosek; J-P Jin
Journal:  Am J Physiol Cell Physiol       Date:  2019-12-25       Impact factor: 4.249

Review 4.  Cardiac myofibrillar proteins: biochemical markers to estimate myocardial injury.

Authors:  K H Haider; W H Stimson
Journal:  Mol Cell Biochem       Date:  1999-04       Impact factor: 3.396

5.  The loss of slow skeletal muscle isoform of troponin T in spindle intrafusal fibres explains the pathophysiology of Amish nemaline myopathy.

Authors:  Kentaro Oki; Bin Wei; Han-Zhong Feng; Jian-Ping Jin
Journal:  J Physiol       Date:  2019-07-03       Impact factor: 5.182

6.  Structure of the NH2-terminal variable region of cardiac troponin T determines its sensitivity to restrictive cleavage in pathophysiological adaptation.

Authors:  Zhiling Zhang; Han-Zhong Feng; J-P Jin
Journal:  Arch Biochem Biophys       Date:  2011-09-05       Impact factor: 4.013

7.  Microtiter plate monoclonal antibody epitope analysis of Ca2+- and Mg2+-induced conformational changes in troponin C.

Authors:  Jian-Ping Jin; Stephen M Chong; M Moazzem Hossain
Journal:  Arch Biochem Biophys       Date:  2007-08-06       Impact factor: 4.013

8.  Loss of mXinalpha, an intercalated disk protein, results in cardiac hypertrophy and cardiomyopathy with conduction defects.

Authors:  Elisabeth A Gustafson-Wagner; Haley W Sinn; Yen-Lin Chen; Da-Zhi Wang; Rebecca S Reiter; Jenny L-C Lin; Baoli Yang; Roger A Williamson; Ju Chen; Cheng-I Lin; Jim J-C Lin
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-08-31       Impact factor: 4.733

9.  Removal of the N-terminal extension of cardiac troponin I as a functional compensation for impaired myocardial beta-adrenergic signaling.

Authors:  Han-Zhong Feng; Min Chen; Lee S Weinstein; Jian-Ping Jin
Journal:  J Biol Chem       Date:  2008-09-24       Impact factor: 5.157

10.  Adaptation by alternative RNA splicing of slow troponin T isoforms in type 1 but not type 2 Charcot-Marie-Tooth disease.

Authors:  Lars Larsson; Xin Wang; Fushun Yu; Peter Höök; Kristian Borg; Stephen M Chong; J-P Jin
Journal:  Am J Physiol Cell Physiol       Date:  2008-06-25       Impact factor: 4.249

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