Sealy Center for Structural Biology and Molecular Biophysics, University of Texas Medical Branch, Galveston, Texas 77555-0857, USA.
Proteins. 2012 May;80(5):1308-15. doi: 10.1002/prot.24027. Epub 2012 Feb 10.
Use of atomic force microscopy (AFM) has recently led to a better understanding of the molecular mechanisms of the unfolding process by mechanical forces; however, the rational design of novel proteins with specific mechanical strength remains challenging. We have approached this problem from a new perspective that generates linear physical-chemical properties (PCP) motifs from a limited AFM data set. Guided by our linear sequence analysis, we designed and analyzed four new mutants of the titin I1 domain with the goal of increasing the domain's mechanical strength. All four mutants could be cloned and expressed as soluble proteins. AFM data indicate that at least two of the mutants have increased molecular mechanical strength. This observation suggests that the PCP method is useful to graft sequences specific for high mechanical stability to weak proteins to increase their mechanical stability, and represents an additional tool in the design of novel proteins besides steered molecular dynamics calculations, coarse grained simulations, and ϕ-value analysis of the transition state.
原子力显微镜(AFM)的使用最近使人们对机械力作用下的蛋白质解折叠过程的分子机制有了更好的理解;然而,设计具有特定机械强度的新型蛋白质仍然具有挑战性。我们从一个新的角度来解决这个问题,即从有限的 AFM 数据集生成线性物理化学性质(PCP)基序。在我们的线性序列分析的指导下,我们设计并分析了 Titin I1 结构域的四个新突变体,目的是增加该结构域的机械强度。这四个突变体都可以被克隆并表达为可溶性蛋白。AFM 数据表明,至少有两个突变体的分子机械强度增加。这一观察结果表明,PCP 方法可用于将特定于高机械稳定性的序列嫁接到弱蛋白上,以提高其机械稳定性,并且是除导向分子动力学计算、粗粒化模拟和过渡态ϕ 值分析之外,设计新型蛋白质的另一种工具。