Burke M, Sivaramakrishnam M, Kamalakannan V
Biochemistry. 1983 Jun 21;22(13):3046-53. doi: 10.1021/bi00282a004.
Evidence is presented that the removal of the alkali light chain subunit from myosin subfragment 1 results in the exposure of a site (or sites) at the carboxyl-terminal region of the heavy chain that is rapidly digested by both trypsin and alpha-chymotrypsin. In the case of trypsin digestion, cleavage at this site proceeds at a much higher rate than cleavage at the two other sensitive regions located in the interior of the primary structure of this chain. This initial cleavage is responsible for the generation, on further digestion with trypsin, of a carboxyl-terminal fragment about 3000 daltons smaller than the corresponding fragment formed by digestion of subfragment 1. The ability of the heavy chain to reassociate with alkali light chain at 4 degrees C in the presence of MgATP is essentially abolished by cleavage at this exposed site by either trypsin or chymotrypsin. These observations indicate that the alkali light chain is binding to, or is capable of perturbing, a region of the heavy chain adjacent to the subfragment 1/subfragment 2 "hinge" region and support recent proposals that both the DTNB light chain and the alkali light chain may be interacting and may be modulating this flexible region of the cross bridge.
有证据表明,从肌球蛋白亚片段1中去除碱性轻链亚基会导致重链羧基末端区域的一个位点(或多个位点)暴露,该位点会被胰蛋白酶和α-糜蛋白酶迅速消化。在胰蛋白酶消化的情况下,该位点的切割速度比位于该链一级结构内部的其他两个敏感区域的切割速度要高得多。这种初始切割导致在用胰蛋白酶进一步消化时产生一个羧基末端片段,该片段比通过亚片段1消化形成的相应片段小约3000道尔顿。在MgATP存在下,重链在4℃与碱性轻链重新结合的能力基本上被胰蛋白酶或糜蛋白酶在这个暴露位点的切割所消除。这些观察结果表明,碱性轻链与重链中亚片段1/亚片段2“铰链”区域相邻的区域结合,或者能够干扰该区域,并且支持最近的提议,即DTNB轻链和碱性轻链可能相互作用,并可能调节横桥的这个柔性区域。