Miki M
J Biochem. 1985 Apr;97(4):1067-72. doi: 10.1093/oxfordjournals.jbchem.a135149.
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.
在几个不同的pH值下,用7-氯-4-硝基苯并-2-恶唑-1,3-二氮杂茂(NBD-氯化物)对肌肉原肌球蛋白进行修饰。NBD-氯化物在中性pH下与SH残基特异性反应,但在碱性pH下它与SH残基和氨基残基都反应。在低离子强度下原肌球蛋白的聚合能力以及原肌球蛋白与F-肌动蛋白的结合特性不受SH残基修饰的影响,但根据之前的报道[约翰逊,P.和斯米利,L.B.(1977年)《生物化学》16,2264 - 2269],它们会因氨基的修饰而迅速丧失。通过添加重酶解肌球蛋白,不能与F-肌动蛋白结合的标记原肌球蛋白恢复了与F-肌动蛋白的结合能力,并且在肌钙蛋白存在的情况下它能够调节肌动球蛋白的超沉淀。氨基的进一步修饰(标记率超过5)导致调节能力完全丧失。