Multiplexed microbead immunoassays by flow cytometry for molecular profiling: Basic concepts and proteomics applications

被引:86
作者
Krishhan, V. V. [1 ,2 ,3 ]
Khan, Imran H. [3 ,4 ]
Luciw, Paul A. [3 ,4 ,5 ]
机构
[1] Calif State Univ Fresno, Dept Chem, Fresno, CA 93740 USA
[2] Dept Appl Sci, Davis, CA 95616 USA
[3] Ctr Comparat Med, Davis, CA 95616 USA
[4] Dept Pathol & Lab Med, Davis, CA 95616 USA
[5] Univ Calif Davis, Calif Natl Primate Res Ctr, Davis, CA 95616 USA
关键词
Flow cytometry; immunoassay; multiplex; biomarker; proteomics; HUMAN-IMMUNODEFICIENCY-VIRUS; RESPIRATORY SYNCYTIAL VIRUS; MICROSPHERE-BASED IMMUNOASSAY; SUSPENSION ARRAY TECHNOLOGY; HUMAN-PAPILLOMAVIRUS TYPES; MILD COGNITIVE IMPAIRMENT; BRANCHED DNA ASSAY; DRIED BLOOD SPOTS; BEAD-BASED ASSAYS; HIGH-THROUGHPUT;
D O I
10.1080/07388550802688847
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Flow cytometry was originally established as an automated method for measuring optical or fluorescence characteristics of cells or particles in suspension. With the enormous increase in development of reliable electronics, lasers, micro-fluidics, as well as many advances in immunology and other fields, flow cytometers have become user-friendlier, less-expensive instruments with an increasing importance for both basic research and clinical applications. Conventional uses of flow cytometry include immunophenotyping of blood cells and the analysis of the cell cycle. Importantly, methods for labeling microbeads with unique combinations of fluorescent spectral signatures have made multiplex analysis of soluble analytes (i.e. the ability to detect multiple targets in a single test sample) feasible by flow cytometry. The result is a rapid, high-throughput, sensitive, and reproducible detection technology for a wide range of biomedical applications requiring detection of proteins (in cells and biofluids) and nucleic acids. Thus, novel methods of flow cytometry are becoming important for diagnostic purposes (e.g. identifying multiple clinical biomarkers for a wide range of diseases) as well as for developing novel therapies (e.g. elucidating drug mechanisms and potential toxicities). In addition, flow cytometry for multiplex analysis, coupled with automated sample handling devices, has the potential to significantly enhance proteomics research, particularly analysis of post-translational modifications of proteins, on a large scale. Inherently, flow cytometry methods are strongly rooted in the laws of the physics of optics, fluidics, and electromagnetism. This review article describes principles and early sources of flow cytometry, provides an introduction to the multiplex microbead technology, and discusses its applications and advantages in comparison to other methods. Anticipated future directions, particularly for translational research in medicine, are also discussed.
引用
收藏
页码:29 / 43
页数:15
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