Department of Physical Chemistry, Faculty of Chemistry and Chemical Technology, University of Ljubljana, Ljubljana.
Protein Sci. 2022 Jul;31(7):e4370. doi: 10.1002/pro.4370.
Intrinsically disordered proteins (IDPs) are abundant in eukaryotic proteomes and preform critical roles in many cellular processes, most often through the association with globular proteins. Despite lacking a stable three-dimensional structure by themselves, they may acquire a defined conformation upon binding globular targets. The most common type of secondary structure acquired by these binding motifs entails formation of an α-helix. It has been hypothesized that such disorder-to-order transitions are associated with a significant free energy penalty due to IDP folding, which reduces the overall IDP-target affinity. However, the exact magnitude of IDP folding penalty in α-helical binding motifs has not been systematically estimated. Here, we report the folding penalty contributions for 30 IDPs undergoing folding-upon-binding and find that the average IDP folding penalty is +2.0 kcal/mol and ranges from 0.7 to 3.5 kcal/mol. We observe that the folding penalty scales approximately linearly with the change in IDP helicity upon binding, which provides a simple empirical way to estimate folding penalty. We analyze to what extent do pre-structuring and target-bound IDP dynamics (fuzziness) reduce the folding penalty and find that these effects combined, on average, reduce the folding cost by around half. Taken together, the presented analysis provides a quantitative basis for understanding the role of folding penalty in IDP-target interactions and introduces a method estimate this quantity. Estimation and reduction of IDP folding penalty may prove useful in the rational design of helix-stabilized inhibitors of IDP-target interactions. STATEMENT: The α-helical binding motifs are ubiquitous among the intrinsically disordered proteins (IDPs). Upon binding their targets, they undergo a disorder-to-order transition, which is accompanied by a significant folding penalty whose magnitude is generally not known. Here, we use recently developed statistical-thermodynamic model to estimate the folding penalties for 30 IDPs and clarify the roles of IDP pre-folding and bound-state dynamics in reducing the folding penalty.
无定形蛋白质(IDPs)在真核生物蛋白质组中大量存在,并在许多细胞过程中发挥关键作用,大多数情况下是通过与球状蛋白质结合来实现的。尽管它们本身没有稳定的三维结构,但在与球状靶标结合时,它们可能会获得确定的构象。这些结合基序获得的最常见的二级结构类型是形成α-螺旋。有人假设,由于 IDP 折叠,这种无序到有序的转变与显著的自由能损失有关,从而降低了整个 IDP-靶标亲和力。然而,α-螺旋结合基序中 IDP 折叠代价的确切幅度尚未系统地估计。在这里,我们报告了 30 个经历折叠的 IDP 的折叠代价贡献,并发现平均 IDP 折叠代价为+2.0 kcal/mol,范围为 0.7 至 3.5 kcal/mol。我们观察到,折叠代价与结合时 IDP 螺旋性的变化大致呈线性关系,这为估计折叠代价提供了一种简单的经验方法。我们分析了预结构化和靶标结合的 IDP 动力学(模糊性)在多大程度上降低了折叠代价,发现这些效应平均而言,降低了约一半的折叠成本。综上所述,所提出的分析为理解折叠代价在 IDP-靶标相互作用中的作用提供了定量基础,并介绍了一种估计该数量的方法。估计和降低 IDP 折叠代价可能有助于合理设计稳定 IDP-靶标相互作用的螺旋抑制剂。