A label-free nanoparticle aggregation assay for protein complex/aggregate detection and study

被引:36
作者
Bogdanovic, Jelena [1 ]
Colon, Jimmie [2 ]
Baker, Cheryl [2 ]
Huo, Qun [1 ]
机构
[1] Univ Cent Florida, NanoSci Technol Ctr, Orlando, FL 32826 USA
[2] MD Anderson Canc Ctr Orlando, Canc Res Inst, Orlando, FL 32827 USA
关键词
Gold nanoparticles; Dynamic light scattering; Protein aggregates; GAPDH; DYNAMIC LIGHT-SCATTERING; III PNEUMOCOCCUS POLYSACCHARIDE; HOMOLOGOUS ANTIBODY; PRECIPITIN REACTION; 2-HYBRID SYSTEM; FLUORESCENCE; ASSOCIATION; PROBES;
D O I
10.1016/j.ab.2010.06.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The detection, analysis, and understanding of protein complexes/aggregates and their formation process are extremely important for biomolecular research, diagnosis, and biopharmaceutical development. Unfortunately, techniques that can be used conveniently for protein complex/aggregate detection and analysis are very limited. Using gold nanoparticle immunoprobes coupled with dynamic light scattering (DLS), we developed a label-free nanoparticle aggregation immunoassay (NanoDLSay) for protein aggregate detection and study. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH), a protein target used routinely in Western blot as a loading control, is demonstrated here as an example. Through this study, we discovered that GAPDH has a strong tendency to form large aggregates in certain buffer solutions at a concentration range of 10-25 mu g/ml. The strong light scattering property of gold nanoparticles immunoprobes greatly enhanced the sensitivity of the dynamic light scattering for protein complex/aggregate detection. In contrast to fluorescence techniques for protein complex and aggregation study, the protein targets do not need to be labeled with fluorescent probe molecules in NanoDLSay. NanoDLSay is a very convenient and sensitive tool for protein complex/aggregate detection and study. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:96 / 102
页数:7
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