| Literature DB >> 25688674 |
Justin Joachim1, Ming Jiang2, Nicole C McKnight3, Michael Howell2, Sharon A Tooze4.
Abstract
This article discusses the issues to consider in the development and implementation of high-throughput screens (HTSs) using both siRNA libraries and small molecule compound collections, in order to discover autophagy regulators in mammalian cells. We discuss how to develop the screen, focusing on the key parameters to establish in order to perform a successful screen. As our understanding of autophagy increases and its impact on human disease is elucidated, this technology can be further exploited to uncover novel genes, which may one day become new therapeutic targets.Entities:
Keywords: Amino acid starvation; Autophagosome; Autophagy; Drug and compound libraries; GFP-LC3; High-throughput screens; Z-score; p62; siRNA
Mesh:
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Year: 2015 PMID: 25688674 DOI: 10.1016/j.ymeth.2015.02.002
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608