小分子
天然产物
高通量筛选
纳米技术
DNA微阵列
微阵列
基因敲除
化学
表型筛选
细胞
计算生物学
材料科学
生物
基因
生物化学
基因表达
表型
作者
Bo Peng,Changmin Yu,Shubo Du,Si Si Liew,Xin Mao,Peiyan Yuan,Zhenkun Na,Shao Q. Yao
出处
期刊:ChemBioChem
[Wiley]
日期:2018-02-21
卷期号:19 (9): 986-996
被引量:16
标识
DOI:10.1002/cbic.201800101
摘要
Standard small-molecule microarrays (SMMs) are not well-suited for cell-based screening assays. Of the few attempts made thus far to render SMMs cell-compatible, all encountered major limitations. Here we report the first mesoporous silica nanoparticle (MSN)-on-a-chip platform capable of allowing high-throughput cell-based screening to be conducted on SMMs. By making use of a glass surface on which hundreds of MSNs, each encapsulated with a different native natural product, were immobilized in spatially defined manner, followed by on-chip mammalian cell growth and on-demand compound release, high-content screening was successfully carried out with readily available phenotypic detection methods. By combining this new MSN-on-a-chip system with small interfering RNA technology for the first time, we discovered that (+)-usniacin possesses synergistic inhibitory properties similar to those of olaparib (an FDA-approved drug) in BRCA1-knockdown cancer cells.
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