Sharma Gaurav, Rege Kaushal, Budil David E, Yarmush Martin L, Mavroidis Constantinos
Department of Mechanical and Industrial Engineering, Northeastern University, Boston, MA 02115, USA.
Int J Nanomedicine. 2008;3(4):505-21. doi: 10.2147/ijn.s4046.
We describe the molecular dynamics (MD)-aided engineering design of mutant peptides based on the alpha-helical coiled-coil GCN4 leucine zipper peptide (GCN4-p1) in order to obtain environmentally-responsive nanotweezers. The actuation mechanism of the nanotweezers depends on the modification of electrostatic charges on the residues along the length of the coiled coil. Modulating the solution pH between neutral and acidic values results in the reversible movement of helices toward and away from each other and creates a complete closed-open-closed transition cycle between the helices. Our results indicate that the mutants show a reversible opening of up to 15 A (1.5 nm; approximately 150% of the initial separation) upon pH actuation. Investigation on the physicochemical phenomena that influence conformational properties, structural stability, and reversibility of the coiled-coil peptide-based nanotweezers revealed that a rationale- and design-based approach is needed to engineer stable peptide or macromolecules into stimuli-responsive devices. The efficacy of the mutant that demonstrated the most significant reversible actuation for environmentally responsive modulation of DNA-binding activity was also demonstrated. Our results have significant implications in bioseparations and in the engineering of novel transcription factors.
我们描述了基于α-螺旋卷曲螺旋GCN4亮氨酸拉链肽(GCN4-p1)的突变肽的分子动力学(MD)辅助工程设计,以获得对环境响应的纳米镊子。纳米镊子的驱动机制取决于卷曲螺旋长度上残基静电电荷的修饰。在中性和酸性值之间调节溶液pH会导致螺旋相互靠近和远离的可逆运动,并在螺旋之间形成完整的闭合-打开-闭合转变循环。我们的结果表明,突变体在pH驱动下显示出高达15 Å(1.5 nm;约为初始间距的150%)的可逆打开。对影响基于卷曲螺旋肽的纳米镊子构象性质、结构稳定性和可逆性的物理化学现象的研究表明,需要一种基于原理和设计的方法来将稳定的肽或大分子设计成刺激响应装置。还展示了对DNA结合活性进行环境响应调节时表现出最显著可逆驱动的突变体的功效。我们的结果在生物分离和新型转录因子的工程设计方面具有重要意义。