Vera-Rodríguez Darex J, Sapienza Paul J, Popov Konstantin I, Lee Andrew L
Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Protein Sci. 2025 Oct;34(10):e70315. doi: 10.1002/pro.70315.
Allostery is a key driver of protein function and behavior in biological systems. Historically, allosteric regulation has been attributed to conformational and dynamic changes, mostly derived from well-structured regions of proteins. While the regulatory contributions of specific unstructured elements, such as catalytic loops near the active site, have been widely characterized, the role of distal, flexible loops remains poorly understood. Here, we investigate the allosteric protein chorismate mutase (CM), a homodimeric enzyme critical for the biosynthesis of aromatic amino acids. Although CM is differentially regulated by tryptophan and tyrosine via a shared pocket over 25 Å from the active site, their near-identical NMR spectra suggest that alternative mechanisms may explain TrpCM and TyrCM's distinct functional landscapes. We demonstrate that a mutation within a structurally invisible and highly flexible loop, loop 11-12, located far from the active site, drastically alters CM's activity landscape. Using paramagnetic labeling of the loop, we show that loop 11-12 undergoes transient excursions toward the active site, but only in the presence of the activator Trp, which binds over 20 Å away. Furthermore, employing a novel NMR approach, we show that loop 11-12 modulates CM's electrostatics, potentially influencing charge distribution to provide another control of enzymatic activity. Our findings support a sophisticated allosteric process in which a flexible, distal loop is functionally coupled to both the effector binding region and the active site. This mechanism provides new insights into the diverse ways proteins achieve allosteric regulation and may contribute to understanding flexible regions in other allosteric systems.
变构是生物系统中蛋白质功能和行为的关键驱动因素。从历史上看,变构调节一直归因于构象和动态变化,这些变化大多源自蛋白质结构良好的区域。虽然特定的非结构化元件(如活性位点附近的催化环)的调节作用已得到广泛表征,但远端柔性环的作用仍知之甚少。在这里,我们研究变构蛋白分支酸变位酶(CM),一种对芳香族氨基酸生物合成至关重要的同二聚体酶。尽管CM通过一个距离活性位点超过25埃的共享口袋受到色氨酸和酪氨酸的差异调节,但其几乎相同的核磁共振光谱表明,其他机制可能解释色氨酸CM和酪氨酸CM不同的功能格局。我们证明,位于远离活性位点的结构不可见且高度柔性的环(环11 - 12)内的一个突变会极大地改变CM的活性格局。通过对该环进行顺磁标记,我们表明环11 - 12会向活性位点进行短暂偏移,但仅在结合位点距离超过20埃的激活剂色氨酸存在时才会发生。此外,采用一种新颖的核磁共振方法,我们表明环11 - 12调节CM的静电作用,可能影响电荷分布以提供对酶活性的另一种控制。我们的研究结果支持一种复杂的变构过程,其中一个柔性远端环在功能上与效应物结合区域和活性位点都耦合。这种机制为蛋白质实现变构调节的多种方式提供了新见解,并可能有助于理解其他变构系统中的柔性区域。