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Thermodynamic Model for the Stabilization of Trigonal Thiolato Mercury(II) in Designed Three-Stranded Coiled Coils

机译:设计的三股螺旋线圈中三角硫氰酸盐(II)稳定化的热力学模型

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摘要

A thermodynamic model is presented that describes the binding of Hg(II) to de novo designed peptides, Tn L9C and Baby L9C, which were derived from the Tn family. The Iii peptides are based on the parent sequence Ac-NH-G(LKALEEK)_xG-CONH_2 and are known to form two-stranded coiled coils at low pH (pH <4) and three-stranded coiled coils at high pH (pH >7). Tn L9C (x = 4) contains a four heptad repeat sequence with cysteine in position 9 and leucines in the other a and d positions; Baby L9C (x = 3). which also has a cysteine in position 9 but is one heptad shorter than Tn L9C, was designed to form less stable helical coiled coils in solution. The free energies of coiled coil formation for Tn, Tn L9C, Baby Tn, and Baby L9C at pH 2.5 and 8.5 were determined by guanidinium denaturation titrations:Tn L9C was observed to be highly helical in the absence of denaturant at pH 8.5 while Baby L9C contained <20% helical content at pH 8.5, indicating a weakly associated or unassociated coiled coil. Size-exclusion chromatography (SEC) verified that Baby L9C was a monomer at pH 8.5. The helicity of Baby L9C was induced by addition of HgCl_2. The subsequent formation of a trigonal thiolato Hg(II) in the interior of a three-stranded coiled coil was verified by the presence of a characteristic HgS_3 UV band at 248 nm. Titrations of Tn L9C and Baby L9C into solutions of HgCI_2 at pH values between 7 and 9 were performed to extract binding constants. Global fits to the data employed a mechanism that involved initial bindine of mercury to the peptides forming a two-stranded coiled coil with linear thiolato Hg(II) at [peptide]/[Hg] <2, followed by addition of a more weakly associated third helix to generate a three-stranded coiled coil. This mechanism would require the deprotonation of the third cysteine thiol to generate the trigonal thiolato Hg(II) at pH >7.5 [the pK_a of the cysteine thiol in the presence of Hg(II)]. Support for this mechanism was given by the observation of a three-stranded coiled coil by SEC in a solution of Tn L9C at pH 7.0.
机译:提出了一个热力学模型,该模型描述了Hg(II)与从Tn家族衍生的从头设计的肽Tn L9C和Baby L9C的结合。 Iii肽基于亲本序列Ac-NH-G(LKALEEK)_xG-CONH_2,已知在低pH值(pH <4)时可形成双链卷曲螺旋,而在高pH值(pH> 7)。 Tn L9C(x = 4)包含4个七肽重复序列,第9位为半胱氨酸,其他a和d位为亮氨酸;婴儿L9C(x = 3)。它在位置9上也有一个半胱氨酸,但比Tn L9C短一个七聚体,旨在在溶液中形成不太稳定的螺旋形线圈。 Tn,Tn L9C,Baby Tn和Baby L9C在pH 2.5和8.5下通过coil胍变性滴定确定了卷曲螺旋形成的自由能:在pH 8.5时不存在变性剂的情况下,观察到Tn L9C是高度螺旋的,而Baby L9C在pH 8.5时,其螺旋含量小于20%,表明弱关联或不关联的卷曲螺旋。尺寸排阻色谱法(SEC)证实Baby L9C是pH 8.5的单体。婴儿L9C的螺旋线是通过添加HgCl_2诱导的。通过在248 nm处存在特征性的HgS_3 UV带,验证了随后在三链卷曲线圈内部形成三角硫醇基Hg(II)。将Tn L9C和Baby L9C滴定到pH值为7至9的HgCl_2溶液中,以提取结合常数。对数据的整体拟合采用了一种机制,该机制涉及汞与肽的初始结合素形成肽的双链卷曲螺旋,其中线性硫醇Hg(II)的[肽] / [Hg] <2,然后添加更弱的缔合第三螺旋产生一个三链盘绕线圈。该机制将要求第三半胱氨酸硫醇去质子化以在pH> 7.5 [存在Hg(II)的情况下半胱氨酸硫醇的pK_a]生成三角硫醇Hg(II)。通过在7.0 pH的Tn L9C溶液中通过SEC观察到三链盘绕线圈,为这一机理提供了支持。

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