Na Yu-Ran, Im Hana
Department of Molecular Biology, Sejong University, Kwangjin-gu, Seoul 143-747, Korea.
Protein Sci. 2007 Aug;16(8):1659-66. doi: 10.1110/ps.072838107. Epub 2007 Jun 28.
Plasminogen activator inhibitor-1 (PAI-1) belongs to the serine protease inhibitor (serpin) protein superfamily. Serpins are unique in that their native forms are not the most thermodynamically stable conformation; instead, a more stable, latent conformation exists. During the transition to the latent form, the first strand of beta-sheet C (s1C) in the serpin is peeled away from the beta-sheet, and the reactive center loop (RCL) is inserted into beta-sheet A, rendering the serpin inactive. To elucidate the contribution of specific interactions in the metastable native form to the latency transition, we examined the effect of mutations at the s1C of PAI-1, specifically in positions P4' through P10'. Several mutations strengthened the interactions between these residues and the core protein, and slowed the transition of the protein from the metastable native form to the latent form. In particular, anchoring of the strand to the protein's hydrophobic core at the beginning (P4' site) and center of the strand (P8' site) greatly retarded the latency transition. Mutations that weakened the interactions at the s1C region facilitated the conformational conversion of the protein to the latent form. PAI-1's overall structural stability was largely unchanged by the mutations, as evaluated by urea-induced equilibrium unfolding monitored via fluorescence emission. Therefore, the mutations likely exerted their effects by modulating the height of the energy barrier from the native to the latent form. Our results show that interactions found only in the metastable native form of serpins are important structural features that attenuate folding of the proteins into their latent forms.
纤溶酶原激活物抑制剂-1(PAI-1)属于丝氨酸蛋白酶抑制剂(serpin)蛋白超家族。丝氨酸蛋白酶抑制剂的独特之处在于其天然形式并非热力学上最稳定的构象;相反,存在一种更稳定的潜伏构象。在向潜伏形式转变的过程中,丝氨酸蛋白酶抑制剂中β折叠C的第一条链(s1C)从β折叠上剥离,反应中心环(RCL)插入β折叠A中,使丝氨酸蛋白酶抑制剂失去活性。为了阐明亚稳态天然形式中特定相互作用对潜伏转变的贡献,我们研究了PAI-1的s1C处的突变效应,特别是在P4'至P10'位置。几个突变增强了这些残基与核心蛋白之间的相互作用,并减缓了蛋白质从亚稳态天然形式向潜伏形式的转变。特别是,链的起始处(P4'位点)和链的中心(P8'位点)与蛋白质疏水核心的锚定极大地延迟了潜伏转变。削弱s1C区域相互作用的突变促进了蛋白质向潜伏形式的构象转化。通过荧光发射监测尿素诱导的平衡去折叠评估,突变对PAI-1的整体结构稳定性影响不大。因此,这些突变可能通过调节从天然形式到潜伏形式的能垒高度来发挥作用。我们的结果表明,仅在丝氨酸蛋白酶抑制剂的亚稳态天然形式中发现的相互作用是重要的结构特征,可减弱蛋白质折叠成其潜伏形式的过程。