Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri.
Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri; Department of Physics, Washington University in St. Louis, St. Louis, Missouri.
Biophys J. 2019 Dec 3;117(11):2120-2140. doi: 10.1016/j.bpj.2019.09.047. Epub 2019 Oct 28.
Escherichia coli single-strand (ss) DNA-binding protein (SSB) is an essential protein that binds ssDNA intermediates formed during genome maintenance. SSB homotetramers bind ssDNA in several modes differing in occluded site size and cooperativity. The 35-site-size ((SSB)) mode favored at low [NaCl] and high SSB/DNA ratios displays high "unlimited" nearest-neighbor cooperativity (ω), forming long protein clusters, whereas the 65-site-size ((SSB)) mode in which ssDNA wraps completely around the tetramer is favored at higher [NaCl] (>200 mM) and displays "limited" cooperativity (ω), forming only dimers of tetramers. In addition, a non-nearest-neighbor high cooperativity can also occur in the (SSB) mode on long ssDNA even at physiological salt concentrations in the presence of glutamate and requires its intrinsically disordered C-terminal linker (IDL) region. However, whether cooperativity exists between the different modes and the role of the IDL in nearest-neighbor cooperativity has not been probed. Here, we combine sedimentation velocity and fluorescence titration studies to examine nearest-neighbor cooperativity in each binding mode and between binding modes using (dT) and (dT). We find that the (SSB) mode always shows extremely high "unlimited" cooperativity that requires the IDL. At high salt, wild-type SSB and a variant without the IDL, SSB-ΔL, bind in the (SSB) mode but show little cooperativity, although cooperativity increases at lower [NaCl] for wild-type SSB. We also find significant intermode nearest-neighbor cooperativity (ω), with ω ≪ ω <ω. The intrinsically disordered region of SSB is required for all cooperative interactions; however, in contrast to the non-nearest-neighbor cooperativity observed on longer ssDNA, glutamate does not enhance these nearest-neighbor cooperativities. Therefore, we show that SSB possesses four types of cooperative interactions, with clear differences in the forces stabilizing nearest-neighbor versus non-nearest-neighbor cooperativity.
大肠杆菌单链(ss)DNA 结合蛋白(SSB)是一种必需的蛋白质,可结合基因组维护过程中形成的 ssDNA 中间体。SSB 同源四聚体以不同的结合模式结合 ssDNA,这些模式在被占据的位点大小和协同性方面存在差异。在低盐浓度和高 SSB/DNA 比例下,35 个碱基大小((SSB))模式有利于形成长的蛋白质簇,而在高盐浓度(>200 mM)下,65 个碱基大小((SSB))模式有利于 ssDNA 完全缠绕四聚体,显示出“有限”的协同性(ω),仅形成四聚体的二聚体。此外,在生理盐浓度下,谷氨酸存在时,即使在生理盐浓度下,非近邻高协同性也会在(SSB)模式的长 ssDNA 上发生,并且需要其内在无序的 C 端连接区(IDL)。然而,不同模式之间是否存在协同性以及 IDL 在近邻协同性中的作用尚未得到探究。在这里,我们结合沉降速度和荧光滴定研究,使用(dT)和(dT)检查每个结合模式和结合模式之间的近邻协同性。我们发现(SSB)模式始终显示出极高的“无限”协同性,需要 IDL。在高盐浓度下,野生型 SSB 和没有 IDL 的变体 SSB-ΔL 以(SSB)模式结合,但协同性很小,尽管野生型 SSB 的[NaCl]较低时协同性增加。我们还发现了显著的模式间近邻协同性(ω),ω<ω<ω。SSB 的无规卷曲区域是所有协同相互作用所必需的;然而,与在较长 ssDNA 上观察到的非近邻协同性相反,谷氨酸不会增强这些近邻协同性。因此,我们表明 SSB 具有四种类型的协同相互作用,在稳定近邻与非近邻协同性的力方面存在明显差异。