Vreuls Christelle, Filée Patrice, Van Melckebeke Hélène, Aerts Tony, De Deyn Peter, Llabrès Gabriel, Matagne André, Simorre Jean-Pierre, Frère Jean-Marie, Joris Bernard
Centre d'ingénierie des Protéines, Institut de Chimie B6a, Université de Liège, Sart-Tilman, B4000 Liège, Belgium.
Biochem J. 2004 Nov 15;384(Pt 1):179-90. doi: 10.1042/BJ20040658.
The Bacillus licheniformis 749/I BlaI repressor is a prokaryotic regulator that, in the absence of a beta-lactam antibiotic, prevents the transcription of the blaP gene, which encodes the BlaP beta-lactamase. The BlaI repressor is composed of two structural domains. The 82-residue NTD (N-terminal domain) is a DNA-binding domain, and the CTD (C-terminal domain) containing the next 46 residues is a dimerization domain. Recent studies have shown the existence of the monomeric, dimeric and tetrameric forms of BlaI in solution. In the present study, we analyse the equilibrium unfolding of BlaI in the presence of GdmCl (guanidinium chloride) using different techniques: intrinsic and ANS (8-anilinonaphthalene-l-sulphonic acid) fluorescence, far- and near-UV CD spectroscopy, cross-linking, analytical ultracentrifugation, size exclusion chromatography and NMR spectroscopy. In addition, the intact NTD and CTD were purified after proteolysis of BlaI by papain, and their unfolding by GdmCl was also studied. GdmCl-induced equilibrium unfolding was shown to be fully reversible for BlaI and for the two isolated fragments. The results demonstrate that the NTD and CTD of BlaI fold/unfold independently in a four-step process, with no significant co-operative interactions between them. During the first step, the unfolding of the BlaI CTD occurs, followed in the second step by the formation of an 'ANS-bound' intermediate state. Cross-linking and analytical ultracentrifugation experiments suggest that the dissociation of the dimer into two partially unfolded monomers takes place in the third step. Finally, the unfolding of the BlaI NTD occurs at a GdmCl concentration of approx. 4 M. In summary, it is shown that the BlaI CTD is structured, more flexible and less stable than the NTD upon GdmCl denaturation. These results contribute to the characterization of the BlaI dimerization domain (i.e. CTD) involved in the induction process.
地衣芽孢杆菌749/I BlaI阻遏蛋白是一种原核调节因子,在不存在β-内酰胺抗生素的情况下,它会阻止编码BlaPβ-内酰胺酶的blaP基因的转录。BlaI阻遏蛋白由两个结构域组成。含82个残基的NTD(N端结构域)是一个DNA结合结构域,接下来含46个残基的CTD(C端结构域)是一个二聚化结构域。最近的研究表明,溶液中存在BlaI的单体、二聚体和四聚体形式。在本研究中,我们使用不同技术分析了在盐酸胍(GdmCl)存在下BlaI的平衡去折叠过程:固有荧光和ANS(8-苯胺基萘-1-磺酸)荧光、远紫外和近紫外圆二色光谱、交联、分析超速离心、尺寸排阻色谱和核磁共振光谱。此外,用木瓜蛋白酶对BlaI进行蛋白水解后,纯化了完整的NTD和CTD,并研究了它们在GdmCl作用下的去折叠情况。结果表明,GdmCl诱导的BlaI及其两个分离片段的平衡去折叠是完全可逆的。结果表明,BlaI的NTD和CTD在一个四步过程中独立折叠/去折叠,它们之间没有明显的协同相互作用。第一步,BlaI的CTD发生去折叠,第二步形成一个“ANS结合”的中间状态。交联和分析超速离心实验表明,第三步二聚体解离成两个部分去折叠的单体。最后,在约4 M的GdmCl浓度下,BlaI的NTD发生去折叠。总之,结果表明,在GdmCl变性时,BlaI的CTD比NTD结构更规整、更灵活且稳定性更低。这些结果有助于对参与诱导过程的BlaI二聚化结构域(即CTD)进行表征。