Department of Biochemistry, School of Biology, Moscow State University, Moscow 119234, Russia.
A.N. Bach Institute of Biochemistry, Federal Research Center "Fundamentals of Biotechnology", Russian Academy of Sciences, Moscow 119071, Russia.
Int J Mol Sci. 2023 Jan 6;24(2):1085. doi: 10.3390/ijms24021085.
The α-crystallin domain (ACD) is the hallmark of a diverse family of small heat shock proteins (sHsps). We investigated some of the ACD properties of five human sHsps as well as their interactions with different full-length sHsps. According to size-exclusion chromatography, at high concentrations, the ACDs of HspB1 (B1ACD), HspB5 (B5ACD) and HspB6 (B6ACD) formed dimers of different stabilities, which, upon dilution, dissociated to monomers to different degrees. Upon dilution, the B1ACD dimers possessed the highest stabilities, and those of B6ACD had the lowest. In striking contrast, the ACDs of HspB7 (B7ACD) and HspB8 (B8ACD) formed monomers in the same concentration range, which indicated the compromised stabilities of their dimer interfaces. B1ACD, B5ACD and B6ACD transiently interacted with full-length HspB1 and HspB5, which are known to form large oligomers, and modulated their oligomerization behavior. The small oligomers formed by the 3D mutant of HspB1 (mimicking phosphorylation at Ser15, Ser78 and Ser82) effectively interacted with B1ACD, B5ACD and B6ACD, incorporating these α-crystallin domains into their structures. The inherently dimeric full-length HspB6 readily formed heterooligomeric complexes with B1ACD and B5ACD. In sharp contrast to the abovementioned ACDs, B7ACD and B8ACD were unable to interact with full-length HspB1, the 3D mutant of HspB1, HspB5 or HspB6. Thus, their high sequence homology notwithstanding, B7ACD and B8ACD differ from the other three ACDs in their inability to form dimers and interact with the full-length small heat shock proteins. Having conservative primary structures and being apparently similar, the ACDs of the different sHsps differ in terms of their dimer stabilities, which can influence the heterooligomerization preferences of sHsps.
α-晶体蛋白结构域(ACD)是小热休克蛋白(sHsps)家族的标志。我们研究了五种人类 sHsps 的一些 ACD 特性以及它们与不同全长 sHsps 的相互作用。根据大小排阻层析,在高浓度下,HspB1(B1ACD)、HspB5(B5ACD)和 HspB6(B6ACD)的 ACD 形成不同稳定性的二聚体,稀释后,二聚体不同程度地解离为单体。稀释后,B1ACD 二聚体具有最高的稳定性,而 B6ACD 的二聚体具有最低的稳定性。与此形成鲜明对比的是,HspB7(B7ACD)和 HspB8(B8ACD)的 ACD 在相同的浓度范围内形成单体,这表明它们的二聚体界面稳定性受损。B1ACD、B5ACD 和 B6ACD 与全长 HspB1 和 HspB5 瞬时相互作用,HspB1 和 HspB5 已知形成大寡聚物,并调节它们的寡聚化行为。HspB1 的 3D 突变体(模拟 Ser15、Ser78 和 Ser82 的磷酸化)形成的小寡聚物有效地与 B1ACD、B5ACD 和 B6ACD 相互作用,将这些 α-晶体蛋白结构域纳入其结构中。天然二聚全长 HspB6 与 B1ACD 和 B5ACD 容易形成异源寡聚复合物。与上述 ACD 形成鲜明对比的是,B7ACD 和 B8ACD 无法与全长 HspB1、HspB1 的 3D 突变体、HspB5 或 HspB6 相互作用。因此,尽管它们具有高度的序列同源性,但 B7ACD 和 B8ACD 与其他三个 ACD 不同,它们不能形成二聚体并与全长小热休克蛋白相互作用。不同 sHsps 的 ACD 具有保守的一级结构,且明显相似,但在二聚体稳定性方面存在差异,这可能影响 sHsps 的异源寡聚化偏好。