Morgan Brittany R, Deveau Laura M, Massi Francesca
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts, Worcester, Massachusetts.
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts, Worcester, Massachusetts.
Biophys J. 2015 Mar 24;108(6):1503-1515. doi: 10.1016/j.bpj.2015.01.039.
A member of the TTP family of proteins, TIS11d binds RNA with high specificity using a pair of CCCH-type tandem zinc fingers separated by a 18 residue long linker. Our previous work showed that the formation of hydrogen bonds between the C-terminal residue E220 and the residues of the linker region stabilized a compact structure of TIS11d in the absence of RNA. To investigate the role of the C-terminal residues in the structure of unbound TIS11d, the E220A mutant and the truncation mutant lacking the last two residues (D219/E220) were studied using molecular dynamics, NMR spectroscopy, and biochemical methods. This study confirmed the importance of the charged residues D219 and E220 in maintaining structural stability in unbound TIS11d and elucidated the underlying physical mechanisms. We observed a greater structural heterogeneity for the residues of the linker in the molecular dynamics trajectories of both mutant proteins relative to the wild-type. This heterogeneity was more pronounced in the D219/E220 deletion mutant than in the E220A mutant, indicating that a greater reduction of the charge of the C-terminus results in greater flexibility. In agreement with the increased flexibility and the reduced number of negatively charged residues of the D219/E220 deletion mutant, we measured more unfavorable entropic and a more favorable enthalpic contribution to the free energy of RNA binding in the mutant than in the wild-type protein. The relative orientation of the zinc fingers was stabilized by the electrostatic interaction between E220 and positively charged residues of the linker in TIS11d. In the E220A mutant, the relative orientation of the zinc fingers was less constrained, whereas in the D219/E220 deletion mutant, little orientational preference was observed. We posit that favorable electrostatic interactions provide a mechanism to promote preferential orientation of separate domains without imposing structural rigidity.
TIS11d是TTP蛋白家族的成员,它利用一对由18个残基长的连接子分隔的CCCH型串联锌指以高特异性结合RNA。我们之前的工作表明,在没有RNA的情况下,C末端残基E220与连接子区域的残基之间形成氢键稳定了TIS11d的紧凑结构。为了研究C末端残基在未结合的TIS11d结构中的作用,使用分子动力学、核磁共振光谱和生化方法研究了E220A突变体和缺少最后两个残基(D219/E220)的截短突变体。这项研究证实了带电荷的残基D219和E220在维持未结合的TIS11d结构稳定性方面的重要性,并阐明了潜在的物理机制。我们观察到,相对于野生型,两种突变蛋白的分子动力学轨迹中连接子残基的结构异质性更大。这种异质性在D219/E220缺失突变体中比在E220A突变体中更明显,表明C末端电荷的更大减少导致更大的灵活性。与D219/E220缺失突变体灵活性增加和带负电荷残基数量减少一致,我们测量到该突变体中RNA结合自由能的熵贡献更不利,焓贡献更有利。在TIS11d中,锌指的相对取向通过E220与连接子带正电荷残基之间的静电相互作用得以稳定。在E220A突变体中,锌指的相对取向受到的限制较小,而在D219/E220缺失突变体中,几乎没有观察到取向偏好。我们认为,有利的静电相互作用提供了一种机制,可促进独立结构域的优先取向,而不会造成结构刚性。