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Updated: Mar 27, 2026

A Guided Materials Screening Approach for Developing Quantitative Sol-gel Derived Protein Microarrays
Published on: August 26, 2013
Proteome Microarray-Guided Global View: Multiple Pharmacological Targets of Icariin
Guichun Gong1, Xianjin Tang1, Guanghun Yuan1
1Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education and Key Laboratory of Basic Pharmacology of Guizhou Province and Laboratory Animal Center, Zunyi Medical University, Zunyi, Guizhou, 563000, People's Republic of China.
Background:
Icariin (ICA) is a major bioactive compound extracted from the traditional Chinese medicinal herb Epimedium, demonstrated a broad spectrum of pharmacological properties. However, a comprehensive and up-to-date study exclusively focusing on ICA direct binding proteins has not yet been conducted.
Methods:
HuProt™ 20K human proteome microarray, the highest capacity human protein microarray, is suitable for the applications of small molecule targeting proteins. Here, we constructed an atlas of the ICA-binding proteins directly via proteome microarray.
Results:
We showed that a total of 246 proteins which directly interacted with ICA. Subsequent PPI network analysis organized these proteins into 4 functionally distinct clusters, revealing that ICA interacts with proteins central to fundamental cellular processes, including protein folding chaperone complexes, the ubiquitin-proteasome system, apoptotic and PI3K-Akt signaling pathways, and nucleotide metabolism.
Conclusion:
This study constructed an atlas of the ICA-binding proteins directly via microarray, which spans protein folding, ubiquitin-proteasome, apoptosis and nucleotide metabolism, providing a theoretical basis for ICA treatment of diseases caused by dysregulation of these core pathways.
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