Teschke C M, King J
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.
Biochemistry. 1995 May 23;34(20):6815-26. doi: 10.1021/bi00020a028.
The coat protein that forms the icosahedral shell of phage P22 can be efficiently refolded in vitro [Teschke, C. M., & King, J. (1993) Biochemistry 32, 10839-10847]. Temperature-sensitive mutants of coat protein interfere with folding or assembly in vivo [Gordon, C. L., & King, J. (1993) J. Biol. Chem. 268, 9358-9368]. The folding of a set of phage P22 coat proteins carrying the temperature-sensitive for folding (tsf) substitutions W48Q, A108V, G232D, T294I, and F353L has been investigated in vitro. Denatured tsf polypeptides were able to fold into soluble species with high efficiency. The efficiency of folding of the wild-type (WT) and mutant polypeptides at different temperatures showed sharp transitions where aggregation predominated over folding. The refolding of the tsf mutant proteins did not show an obvious thermal defect in yield. The tsf polypeptides folded through the long-lived kinetic intermediate previously described for WT coat protein with similar relaxation times. The folding kinetics of the tsf polypeptides in bisANS, a hydrophobic fluorescent dye, were also similar to those of the WT protein. However, the folded tsf proteins showed decreased secondary structure compared to WT coat protein. Analysis of the folded state by native gel electrophoresis revealed that the tsf coat proteins folded into dimers and trimers, not monomers. The dimer and trimer species were incompetent for assembly. Once formed, dimers and trimers showed no propensity toward aggregation. The folding pathway of the mutant polypeptides must be quite similar to the WT pathway, but at some step inappropriate intersubunit interactions occur due to the amino acid substitutions, trapping the subunits from assembly.
形成噬菌体P22二十面体外壳的衣壳蛋白能够在体外高效重折叠[Teschke, C. M., & King, J. (1993) Biochemistry 32, 10839 - 10847]。衣壳蛋白的温度敏感突变体在体内会干扰折叠或组装过程[Gordon, C. L., & King, J. (1993) J. Biol. Chem. 268, 9358 - 9368]。已经对一组携带折叠温度敏感(tsf)替代突变W48Q、A108V、G232D、T294I和F353L的噬菌体P22衣壳蛋白进行了体外折叠研究。变性的tsf多肽能够高效折叠成可溶性产物。野生型(WT)和突变多肽在不同温度下的折叠效率显示出明显的转变,此时聚集作用超过折叠作用。tsf突变蛋白的重折叠在产量上没有表现出明显的热缺陷。tsf多肽通过先前描述的野生型衣壳蛋白的长寿命动力学中间体进行折叠,且弛豫时间相似。tsf多肽在疏水荧光染料bisANS中的折叠动力学也与野生型蛋白相似。然而,与野生型衣壳蛋白相比,折叠后的tsf蛋白二级结构减少。通过天然凝胶电泳对折叠态进行分析发现,tsf衣壳蛋白折叠成二聚体和三聚体,而非单体。二聚体和三聚体物种无法进行组装。一旦形成,二聚体和三聚体没有聚集倾向。突变多肽的折叠途径必定与野生型途径非常相似,但由于氨基酸替代,在某个步骤会发生不适当的亚基间相互作用,从而阻碍亚基的组装。