Zhou Yicheng, Zhang Yuyu, Rosi Nathaniel L
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.
Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States.
Langmuir. 2024 Jul 17;40(30):15700-9. doi: 10.1021/acs.langmuir.4c01531.
Realizing the promise of chiral inorganic nanomaterials hinges on improving their structural stability under various chemical and environmental conditions. Here, we examine the stability of 1-D gold nanoparticle (Au NP) single helices prepared using the amphiphilic peptide conjugate C-(PEP) (PEP = AYSSGAPPMPPF; = 16-22). We present a general template-independent strategy of tuning helix stability that relies on controlling the dimensions of constituent NPs. As NP dimensions increase, Au NP single helices become both more thermally stable and more stable in the presence of chemical denaturants and protein digestion agents (e.g., urea and proteinase K, respectively). We use this strategy for imparting helix stability to create colloidal suspensions of thermally robust Au NP single helices which maintain their plasmonic chiroptical activity up to ∼80 °C.
实现手性无机纳米材料的前景取决于提高它们在各种化学和环境条件下的结构稳定性。在此,我们研究了使用两亲性肽共轭物C-(PEP)(PEP = AYSSGAPPMPPF; = 16 - 22)制备的一维金纳米颗粒(Au NP)单螺旋的稳定性。我们提出了一种通用的、与模板无关的调节螺旋稳定性的策略,该策略依赖于控制组成纳米颗粒的尺寸。随着纳米颗粒尺寸的增加,Au NP单螺旋在热稳定性以及在化学变性剂和蛋白质消化剂(分别例如尿素和蛋白酶K)存在的情况下都变得更加稳定。我们使用这种赋予螺旋稳定性的策略来创建热稳定的Au NP单螺旋的胶体悬浮液,其在高达约80°C的温度下仍保持其等离子体圆二色活性。