No abstract

Surface-enhanced Raman scattering (SERS)-active nanomaterials have extended from noble metals and transition metals to semiconductor materials, since the first discovery of SERS in the mid-1970s. In comparison with metal substrates and transition metals, semiconductor materials have additional optical and electrical properties besides SERS enhancement ability, which enable them to display remarkable charge-transfer enhancement and catalytic ability. Moreover, their superior biocompatibility allows these nanomaterials to have great potential applications in bioscience. Herein we highlight the fast growing research field focusing on SERS-active semiconductor nanomaterials and semiconductor-other material heterostructures developed in our group as well as in other related research studies. The material size, morphology and assembly-dependent SERS enhancement have been discussed in detail. Furthermore, a variety of promising applications of semiconductor-enhanced Raman scattering in photoelectric characterization, redox biochemistry, sensing, and the catalytic degradation of organic pollutants are introduced.

Proteins are essential components of organisms and they participate in every process within cells. The key characteristic of proteins that allows their diverse functions is their ability to bind other molecules specifically and tightly. With the development of proteomics, exploring high-efficiency detection methods for large-scale proteins is increasingly important. In recent years, rapid development of surface-enhanced Raman scattering (SERS)-based biosensors leads to the SERS realm of applications from chemical analysis to nanostructure characterization and biomedical applications. For proteins, early studies focused on investigating SERS spectra of individual proteins, and the successful design of nanoparticle probes has promoted great progress of SERS-based immunoassays. In this review we outline the development of SERS-based methods for proteins with particular focus on our proposed protein-mediated SERS-active substrates and their applications in label-free and Raman dye-labeled protein detection.

We detected concentration-dependent surface-enhanced Raman scattering (SERS) spectra of several label-free proteins (lysozyme, ribonuclease B, avidin, catalase, and hemoglobin) for the first time in aqueous solutions. Acidified sulfate was used as an aggregation agent to induce high electromagnetic enhancement in SERS. Strong SERS spectra of simple and conjugated protein samples could easily be accessed after the pretreatment with the aggregation agent. The detection limits of the proposed method for lysozyme and catalase were as low as 5 microg/mL and 50 ng/mL, respectively. This detection protocol for label-free proteins has combined simplicity, sensitivity, and reproducibility and allows routine qualitative and relatively quantitative detections. Thus, it has great potential in practical high-throughput protein detections.