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Optimization of Rolling-Circle Amplified Protein Microarrays for Multiplexed Protein Profiling

Protein microarray-based approaches are increasingly being used in research and clinical applications to either profile the expression of proteins or screen molecular interactions. The development of high-throughput, sensitive, convenient, and cost-effective formats for detecting proteins is a neces...

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Detalles Bibliográficos
Autores principales: Shao, Weiping, Zhou, Zhimin, Laroche, Isabelle, Lu, Hong, Zong, Qiuling, Patel, Dhavalkumar D., Kingsmore, Stephen, Piccoli, Steven P.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC521503/
https://www.ncbi.nlm.nih.gov/pubmed/14688416
http://dx.doi.org/10.1155/S1110724303209268
Descripción
Sumario:Protein microarray-based approaches are increasingly being used in research and clinical applications to either profile the expression of proteins or screen molecular interactions. The development of high-throughput, sensitive, convenient, and cost-effective formats for detecting proteins is a necessity for the effective advancement of understanding disease processes. In this paper, we describe the generation of highly multiplexed, antibody-based, specific, and sensitive protein microarrays coupled with rolling-circle signal amplification (RCA) technology. A total of 150 cytokines were simultaneously detected in an RCA sandwich immunoassay format. Greater than half of these proteins have detection sensitivities in the pg/mL range. The validation of antibody microarray with human serum indicated that RCA-based protein microarrays are a powerful tool for high-throughput analysis of protein expression and molecular diagnostics.