Phelan Paul, Gorfe Alemayehu A, Jelesarov Ilian, Marti Daniel N, Warwicker James, Bosshard Hans Rudolf
Biochemisches Institut der Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.
Biochemistry. 2002 Mar 5;41(9):2998-3008. doi: 10.1021/bi011920c.
Interhelical salt bridges are common in leucine zippers and are thought to stabilize the coiled coil conformation. Here we present a detailed thermodynamic investigation of the designed, disulfide-linked leucine zipper AB(SS) whose high-resolution NMR structure shows six interhelical ion pairs between heptad positions g of one helix and e' of the other helix but no ion pairing within single helices. The average pK(a) value of the Glu side chain carboxyl groups of AB(SS) is slightly higher than the pK(a) of a freely accessible Glu in an unfolded peptide [Marti, D. N., Jelesarov, I., and Bosshard, H. R. (2000) Biochemistry 39, 12804-12818]. This indicates that the salt bridges are destabilizing, a prediction we now have confirmed by determining the pH +/- stability profile of AB(SS). Circular dichroism-monitored unfolding by urea and by heating and differential scanning calorimetry show that the coiled coil conformation is approximately 5 kJ/mol more stable when salt bridges are broken by protonation of the carboxyl side chains. Using guanidinium chloride as the denaturant, the increase in the free energy of unfolding on protonation of the carboxyl side chains is larger, approximately 17 kJ/mol. The discrepancy between urea and guanidinium chloride unfolding can be ascribed to the ionic nature of guanidinium chloride, which screens charge-charge interactions. This work demonstrates the difficulty of predicting the energetic contribution of salt bridges from structural data alone even in a case where the ion pairs are seen in high-resolution NMR structures. The reason is that the contribution to stability results from a fine balance between energetically favorable Coulombic attractions and unfavorable desolvation of charges and conformational constraints of the residues involved in ion pairing. The apparent discrepancy between the results presented here and mutational studies indicating stabilization by salt bridges is discussed and resolved. An explanation is proposed for why interhelical salt bridges are frequently found in natural coiled coils despite evidence that they do not directly contribute to stability.
螺旋间盐桥在亮氨酸拉链中很常见,被认为能稳定卷曲螺旋构象。在此,我们对设计的、通过二硫键连接的亮氨酸拉链AB(SS)进行了详细的热力学研究,其高分辨率NMR结构显示在一个螺旋的七肽位置g与另一个螺旋的e'之间有六个螺旋间离子对,但单个螺旋内没有离子配对。AB(SS)的Glu侧链羧基的平均pK(a)值略高于未折叠肽中自由可及的Glu的pK(a) [Marti, D. N., Jelesarov, I., and Bosshard, H. R. (2000) Biochemistry 39, 12804 - 12818]。这表明盐桥是去稳定化的,我们现在通过测定AB(SS)的pH +/-稳定性曲线证实了这一预测。通过尿素、加热以及差示扫描量热法进行的圆二色性监测的去折叠实验表明,当羧基侧链质子化破坏盐桥时,卷曲螺旋构象的稳定性增加约5 kJ/mol。使用氯化胍作为变性剂时,羧基侧链质子化导致的去折叠自由能增加更大,约为17 kJ/mol。尿素和氯化胍去折叠之间的差异可归因于氯化胍的离子性质,它屏蔽了电荷 - 电荷相互作用。这项工作表明,即使在高分辨率NMR结构中能看到离子对的情况下,仅从结构数据预测盐桥的能量贡献也很困难。原因是对稳定性的贡献源于能量上有利的库仑吸引力与电荷去溶剂化以及离子配对中涉及的残基的构象限制之间的精细平衡。本文给出的结果与表明盐桥具有稳定作用的突变研究之间明显的差异也进行了讨论并得到了解决。对于尽管有证据表明螺旋间盐桥并不直接有助于稳定性,但在天然卷曲螺旋中却经常发现它们的原因,我们提出了一种解释。