Department of Biochemistry and Biophysics, University of Kalyani, Kalyani, 741235, West Bengal, India.
Cell Stress Chaperones. 2023 Nov;28(6):689-696. doi: 10.1007/s12192-023-01392-3. Epub 2023 Nov 1.
Inclusion body-associated proteins IbpA and IbpB of MW 16 KDa are the two small heat-shock proteins (sHSPs) of Escherichia coli, and they have only holding, but not folding, chaperone activity. In vitro holdase activity of IbpB is more than that of IbpA, and in combination, they synergise. Both IbpA and IbpB monomers first form homodimers, which as building blocks subsequently oligomerize to make heavy oligomers with MW of MDa range; for IbpB, the MW range of heavy oligomers is 2.0-3.0 MDa, whereas for IbpA oligomers, the values in MDa are not so specified/reported. By temperature upshift, such large oligomers of IbpB, but not of IbpA, dissociate to make relatively small oligomeric assemblies of MW around 600-700KDa. The larger oligomers of IbpB are assumed to be inactive storage form, which on facing heat or oxidative stress dissociate into smaller oligomers of ATP-independent holding chaperone activity. These smaller oligomers bind with stress-induced partially denatured/unfolded and thereby going to be aggregated proteins, to give them protection against permanent damage and aggregation. On withdrawal of stress, IbpB transfers the bound substrate protein to the ATP-dependent bi-chaperone system DnaKJE-ClpB, having both holdase and foldase properties, to finally refold the protein. Of the two sHSPs IbpA and IbpB of E. coli, this review covers the recent advances in research on IbpB only.
MW16kDa 的包涵体相关蛋白 IbpA 和 IbpB 是大肠杆菌的两种小热休克蛋白 (sHSPs),它们只有持留,而没有折叠的伴侣活性。IbpB 的体外持留酶活性大于 IbpA,并且两者结合时具有协同作用。IbpA 和 IbpB 单体首先形成同源二聚体,作为构建块随后寡聚化形成具有 MDa 范围的重寡聚物;对于 IbpB,重寡聚物的 MW 范围为 2.0-3.0 MDa,而对于 IbpA 寡聚物,MDa 中的值没有具体/报道。通过温度升高,IbpB 的这种大寡聚物而非 IbpA 的大寡聚物解离形成 MW 约为 600-700kDa 的相对较小的寡聚体组装体。较大的 IbpB 寡聚物被认为是无活性的储存形式,当面临热或氧化应激时,它会解离成具有 ATP 非依赖性持留伴侣活性的较小寡聚物。这些较小的寡聚物与应激诱导的部分变性/未折叠的蛋白质结合,从而对它们进行保护,防止永久性损伤和聚集。在应激消除后,IbpB 将结合的底物蛋白转移到具有持留酶和折叠酶特性的 ATP 依赖性双伴侣系统 DnaKJE-ClpB 中,最终使蛋白质重新折叠。在大肠杆菌的两种 sHSPs IbpA 和 IbpB 中,本综述仅涵盖了 IbpB 研究的最新进展。