Chemical Modification of Tropomyosin with NBD-Chloride
- 1 April 1985
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Biochemistry
- Vol. 97 (4) , 1067-1072
- https://doi.org/10.1093/oxfordjournals.jbchem.a135149
Abstract
Muscle tropomyosin was modified with 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole (NBD-chloride) at several different pH values. NBD-chloride reacts specifically with SH residue at neutral pH but it reacts with both SH residue and amino residues at alkaline pH. The polymerizability of tropomyosin at low ionic strength and the binding property of tropomyosin to F-actin were not affected by the modification of SH residues but they were lost rapidly by the modification of amino groups, in accordance with the previous report [Johnson, P. & Smillie, L.B. (1977) Biochemistry 16, 2264–2269]. By the addition of heavy meromyosin, labeled tropomyosin which could not bind to F-actin recovered the binding ability to F-actin and it could regulate the superprecipitation of actomyosin in the presence of troponin. Further modification of amino groups (labeling ratios more than 5) led to loss of the regulating ability completely.This publication has 7 references indexed in Scilit:
- Fluorescence energy transfer between ϵ-ATP at the nucleotide binding site and N-(4-dimethylamino-3,5-dinitrophenyl)-maleimide at Cys-373 of G-actinBiochimica et Biophysica Acta (BBA) - Protein Structure, 1978
- The amino acid sequence of rabbit skeletal alpha-tropomyosin. The NH2-terminal half and complete sequenceJournal of Biological Chemistry, 1978
- Polymerizability of rabbit skeletal tropomyosin: effects of enzymic and chemical modificationsBiochemistry, 1977
- Tropomyosin Binding to F-Actin Induced by Myosin HeadsScience, 1976
- Molecular Weight and Subunit Structure of Tropomyosin BJournal of Biological Chemistry, 1967
- Interaction of tropomyosin with actinArchives of Biochemistry and Biophysics, 1964
- Studies on the structure of myosinJournal of Molecular Biology, 1962