Department of Chemistry and ‡Laufer Center for Physical and Quantitative Biology, Stony Brook University , Stony Brook, New York 11794-3400, United States.
J Am Chem Soc. 2016 Dec 7;138(48):15682-15689. doi: 10.1021/jacs.6b09511. Epub 2016 Nov 21.
The rational and predictable enhancement of protein stability is an important goal in protein design. Most efforts target the folded state, however stability is the free energy difference between the folded and unfolded states thus both are suitable targets. Strategies directed at the unfolded state usually seek to decrease chain entropy by introducing cross-links or by replacing glycines. Cross-linking has led to mixed results. Replacement of glycine with an l-amino acid, while reducing the entropy of the unfolded state, can introduce unfavorable steric interactions in the folded state, since glycine is often found in conformations that require a positive φ angle such as helical C-capping motifs or type I' and II″ β-turns. l-Amino acids are strongly disfavored in these conformations, but d-amino acids are not. However, there are few reported examples and conflicting results have been obtained when glycines are replaced with d-Ala. We critically examine the effect of Gly-to-d-Ala substitutions on protein stability using experimental approaches together with molecular dynamics simulations and free energy calculations. The data, together with a survey of high resolution structures, show that the vast majority of proteins can be stabilized by substitution of C-capping glycines with d-Ala. Sites suitable for substitutions can be identified via sequence alignment with a high degree of success. Steric clashes in the native state due to the new side chain are rarely observed, but are likely responsible for the destabilizing or null effect observed for the small subset of Gly-to-d-Ala substitutions which are not stabilizing. Changes in backbone solvation play less of a role. Favorable candidates for d-Ala substitution can be identified using a rapid algorithm based on molecular mechanics.
理性且可预测地增强蛋白质稳定性是蛋白质设计的重要目标。大多数努力都针对折叠状态,然而稳定性是折叠状态和未折叠状态之间的自由能差异,因此两者都是合适的目标。针对未折叠状态的策略通常旨在通过引入交联或取代甘氨酸来降低链熵。交联导致了混合的结果。用 l-氨基酸取代甘氨酸虽然降低了未折叠状态的熵,但可能在折叠状态下引入不利的空间相互作用,因为甘氨酸通常存在需要正 φ 角的构象,如螺旋 C 帽基序或 I 型和 II'型 β 转角。l-氨基酸在这些构象中强烈不利,而 d-氨基酸则不是。然而,报道的例子很少,并且当用 d-Ala 取代甘氨酸时,得到了相互矛盾的结果。我们使用实验方法以及分子动力学模拟和自由能计算来批判性地研究 Gly-to-d-Ala 取代对蛋白质稳定性的影响。这些数据,以及对高分辨率结构的调查,表明绝大多数蛋白质可以通过用 d-Ala 取代 C 帽甘氨酸来稳定。通过与具有高度成功率的序列比对,可以识别适合取代的位点。由于新侧链在天然状态下的空间冲突很少观察到,但可能是导致一小部分 Gly-to-d-Ala 取代物不稳定或无效应的原因,这些取代物不能稳定蛋白质。骨架溶剂化的变化作用较小。可以使用基于分子力学的快速算法识别 d-Ala 取代的有利候选物。