Department of Chemistry, University of Miami, Coral Gables, Florida 33124, United States.
J Am Chem Soc. 2011 Aug 17;133(32):12346-9. doi: 10.1021/ja203726n. Epub 2011 Jul 21.
The ability to control the size, shape, composition, and activity of nanomaterials presents a formidable challenge. Peptide approaches represent new avenues to achieve such control at the synthetic level; however, the critical interactions at the bio/nano interface that direct such precision remain poorly understood. Here we present evidence to suggest that materials-directing peptides bind at specific time points during Pd nanoparticle (NP) growth, dictated by material crystallinity. As such surfaces are presented, rapid peptide binding occurs, resulting in the stabilization and size control of single-crystal NPs. Such specificity suggests that peptides could be engineered to direct the structure of nanomaterials at the atomic level, thus enhancing their activity.
控制纳米材料的尺寸、形状、组成和活性是一项艰巨的挑战。肽方法代表了在合成水平上实现这种控制的新途径;然而,在生物/纳米界面上指导这种精确性的关键相互作用仍未得到很好的理解。在这里,我们提出的证据表明,在钯纳米粒子(NP)生长过程中,材料导向肽在特定的时间点结合,这取决于材料的结晶度。随着这些表面的出现,快速的肽结合发生,导致单晶 NP 的稳定和尺寸控制。这种特异性表明,可以设计肽来在原子水平上指导纳米材料的结构,从而提高它们的活性。