p-NN′-phenylenebismaleimide, a specific cross-linking agent for F-actin
- 1 December 1978
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 175 (3), 1023-1032
- https://doi.org/10.1042/bj1751023
Abstract
Covalent cross-links can be inserted between the subunits of F-actin by using p-NN′-phenylenebismaleimide. Cross-linking reaches its maximum value when one molecule of reagent has reacted with each actin subunit. p-NN′-Phenylenebismaleimide reacts initially with a cysteine residue on one subunit, the slower cross-linking reaction involving a lysine residue on a neighbouring subunit. Hydrolysis of the actin-bound reagent limits the extent of cross-linking. Quantitative analysis of the amounts of cross-linked oligomers seen on polyacrylamide gels containing sodium dodecyl sulphate suggests that neither the binding of the reagent to actin nor the formation of cross-links introduces strain into the structure. The cross-links do not join together different F-actin filaments, and evidence is presented that suggests that the cross-links join subunits of the same long-pitched helix.This publication has 20 references indexed in Scilit:
- Crystals of skeletal muscle actin: Pancreatic DNAase I complexFEBS Letters, 1977
- Crystallization of native striated‐muscle actinFEBS Letters, 1977
- Physical and chemical properties of rabbit muscle phosphofructokinase crosslinked with dimethyl suberimidateBiochemistry, 1974
- Molecular control mechanisms in muscle contraction.Physiological Reviews, 1973
- Regulation of muscle contraction. Effect of calcium on the affinity of troponin for actin and tropomyosinBiochemistry, 1973
- A new protein of the thick filaments of vertebrate skeletal myofibrilsJournal of Molecular Biology, 1973
- The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin.1971
- Optical diffraction studies of myofibrillar structurePhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1971
- Actin from Heart Muscle: Isolation, Purification, and Physicochemical PropertiesCirculation Research, 1963
- Tissue sulfhydryl groupsArchives of Biochemistry and Biophysics, 1959