Placido Tiziana, Tognaccini Lorenzo, Howes Barry D, Montrone Alessandro, Laquintana Valentino, Comparelli Roberto, Curri M Lucia, Smulevich Giulietta, Agostiano Angela
CNR-IPCF Istituto per I Processi Chimico-Fisici, S.S. Bari, c/o Dip. Chimica, Via Orabona 4, 70126 Bari, Italy.
Dipartimento di Chimica "Ugo Schiff", Università di Firenze, Via della Lastruccia 3-13, Sesto Fiorentino, 50019 Florence, Italy.
ACS Omega. 2018 May 31;3(5):4959-4967. doi: 10.1021/acsomega.8b00719. Epub 2018 May 7.
The surface of gold nanorods (Au NRs) has been appropriately engineered to achieve a suitable interface for bioconjugation with horse heart cytochrome (HCc). HCc, an extensively studied and well-characterized protein, represents an ideal model for nanoparticle (NP)-protein conjugation studies because of its small size, high stability, and commercial availability. Here, the native state of the protein has been demonstrated for the first time, by means of Raman spectroscopy, to be retained upon conjugation with the anisotropic Au nanostructures, thus validating the proposed protocol as specifically suited to mostly preserve the plasmonic properties of the NRs and to retain the structure of the protein. The successful creation of such bioconjugates with the retention of the protein structure and function along with the preservation of the NP properties represents a challenging but essential task, as it provides the only way to access functional hybrid systems with potential applications in biotechnology, medicine, and catalysis. In this perspective, the organic capping surrounding the Au NRs plays a key role, as it represents the functional interface for the conjugation step. Cetyltrimethylammonium bromide-coated Au NRs, prepared by using a seed-mediated synthetic route, have been wrapped with polyacrylic acid (PAA) by means of electrostatic interactions following a layer-by-layer approach. The resulting water-dispersible negatively charged AuNRs@PAA NPs have then been electrostatically bound to the positively charged HCc. The bioconjugation procedure has been thoroughly monitored by the combined analysis of UV-vis absorption, resonance Raman and Fourier transform infrared spectroscopies, transmission electron microscopy microscopy, and ζ-potential, which verified the successful conjugation of the protein to the nanorods.
金纳米棒(Au NRs)的表面已进行了适当的工程设计,以实现与马心细胞色素(HCc)生物共轭的合适界面。HCc是一种经过广泛研究且特性明确的蛋白质,由于其尺寸小、稳定性高且可商业获取,是纳米颗粒(NP)-蛋白质共轭研究的理想模型。在此,通过拉曼光谱首次证明,该蛋白质的天然状态在与各向异性金纳米结构共轭后得以保留,从而验证了所提出的方案特别适合在很大程度上保留纳米棒的等离子体特性并保留蛋白质的结构。成功制备出这种保留蛋白质结构和功能以及保留NP特性的生物共轭物是一项具有挑战性但又至关重要的任务,因为它提供了获得在生物技术、医学和催化领域具有潜在应用的功能性混合系统的唯一途径。从这个角度来看,Au NRs周围的有机封端起着关键作用,因为它代表了共轭步骤的功能界面。通过种子介导的合成路线制备的十六烷基三甲基溴化铵包覆的Au NRs,采用逐层方法通过静电相互作用用聚丙烯酸(PAA)进行了包裹。随后,所得的水分散性带负电荷的AuNRs@PAA NPs通过静电作用与带正电荷的HCc结合。通过紫外可见吸收光谱、共振拉曼光谱和傅里叶变换红外光谱、透射电子显微镜以及ζ电位的联合分析,对生物共轭过程进行了全面监测,证实了蛋白质与纳米棒成功共轭。