Das Gobind, Mecarini Federico, Gentile Francesco, De Angelis Francesco, Mohan Kumar Hg, Candeloro Patrizio, Liberale Carlo, Cuda Giovanni, Di Fabrizio Enzo
Dipartimento di Medicina Sperimentale e Clinica, Lab BIONEM, Università Magna Graecia di Catanzaro, Catanzaro, Italy.
Biosens Bioelectron. 2009 Feb 15;24(6):1693-9. doi: 10.1016/j.bios.2008.08.050. Epub 2008 Sep 10.
We have illustrated the fabrication of nano-structures as a surface enhanced Raman scattering (SERS) substrate using electro-plating and electron-beam lithography techniques to obtain an array of gold nanograin-aggregate structures of diameter ranging between 80 and 100 nm with interstitial gap of 10-30 nm. The nanostructure based SERS substrate permits us to have better control and reproducibility on generation of plasmon polaritons. The calculation shows the possible detection of myoglobin concentration down to attomole. This SERS substrate is used to investigate the structural changes of different proteins; lysozyme, ribonuclease-B, bovin serum albumin and myoglobin in the temperature range between -65 and 90 degrees C. The in-depth analysis even for small conformational changes is performed using 2D Raman correlation analysis and difference Raman analysis in order to gain straightforward understanding of proteins undergoing thermodynamical perturbation.
我们展示了利用电镀和电子束光刻技术制备作为表面增强拉曼散射(SERS)基底的纳米结构,以获得直径在80至100纳米之间、间隙为10 - 30纳米的金纳米颗粒聚集体阵列。基于纳米结构的SERS基底使我们能够更好地控制和再现表面等离激元极化激元的产生。计算结果表明,有可能检测低至阿托摩尔浓度的肌红蛋白。这种SERS基底用于研究不同蛋白质(溶菌酶、核糖核酸酶 - B、牛血清白蛋白和肌红蛋白)在 - 65至90摄氏度温度范围内的结构变化。为了直接了解经历热力学扰动的蛋白质,使用二维拉曼相关分析和差分拉曼分析对即使是微小的构象变化进行了深入分析。