Boussouf Sabrina E, Agianian Bogos, Bullard Belinda, Geeves Michael A
Protein Sciences Group, Department of Biosciences, University of Kent at Canterbury CT2 7NJ, UK.
J Mol Biol. 2007 Oct 26;373(3):587-98. doi: 10.1016/j.jmb.2007.07.066. Epub 2007 Aug 14.
Lethocerus indirect flight muscle has two isoforms of troponin C, TnC-F1 and F2, which are unusual in having only a single C-terminal calcium binding site (site IV, isoform F1) or one C-terminal and one N-terminal site (sites IV and II, isoform F2). We show here that thin filaments assembled from rabbit actin and Lethocerus tropomyosin (Tm) and troponin (Tn) regulate the binding of rabbit myosin to rabbit actin in much the same way as the mammalian regulatory proteins. The removal of calcium reduces the rate constant for S1 binding to regulated actin about threefold, independent of which TmTn is used. This is consistent with calcium removal causing the TmTn to occupy the B or blocked state to about 70% of the total. The mid point pCa for the switch differed for TnC-F1 and F2 (pCa 6.9 and 6.0, respectively) consistent with the reported calcium affinities for the two TnCs. Equilibrium titration of S1 binding to regulated actin filaments confirms calcium regulated binding of S1 to actin and shows that in the absence of calcium the three actin filaments (TnC-F1, TnC-F2 and mammalian control) are almost indistinguishable in terms of occupancy of the B and C states of the filament. In the presence of calcium TnC-F2 is very similar to the control with approximately 80% of the filament in the C-state and 10-15% in the fully on M-State while TnC-F1 has almost 50% in each of the C and M states. This higher occupancy of the M-state for TnC-F1, which occurs above pCa 6.9, is consistent with this isoform being involved in the calcium activation of stretch activation. However, it leaves unanswered how a C-terminal calcium binding site of TnC can activate the thin filament.
大田鳖间接飞行肌有两种肌钙蛋白C亚型,即TnC-F1和F2,其不同寻常之处在于,仅具有一个C端钙结合位点(位点IV,F1亚型)或一个C端和一个N端位点(位点IV和II,F2亚型)。我们在此表明,由兔肌动蛋白、大田鳖原肌球蛋白(Tm)和肌钙蛋白(Tn)组装而成的细肌丝,调节兔肌球蛋白与兔肌动蛋白结合的方式,与哺乳动物调节蛋白的方式大致相同。去除钙会使S1与受调节肌动蛋白结合的速率常数降低约三倍,这与使用哪种TmTn无关。这与去除钙导致TmTn占据B或阻断状态至总量的约70%是一致的。TnC-F1和F2的转换中点pCa不同(分别为pCa 6.9和6.0),这与报道的两种TnC的钙亲和力一致。S1与受调节肌动蛋白丝结合的平衡滴定证实了S1与肌动蛋白的钙调节结合,并表明在没有钙的情况下,三条肌动蛋白丝(TnC-F1、TnC-F2和哺乳动物对照)在肌丝B和C状态的占据情况几乎无法区分。在有钙的情况下,TnC-F2与对照非常相似,约80%的肌丝处于C状态,10 - 15%处于完全开启的M状态,而TnC-F1在C和M状态各有近50%。在pCa 6.9以上出现的TnC-F1的M状态更高占据率,与该亚型参与拉伸激活的钙激活一致。然而,TnC的C端钙结合位点如何激活细肌丝仍未得到解答。