Authors: An Zhou, Roger P. Simon, Larry David
Addresses: Neuroscience Institute, Morehouse School of Medicine, 720 Westview Dr SW, Atlanta, GA 30310, USA. ' Neuroscience Institute, Morehouse School of Medicine, 720 Westview Dr SW, Atlanta, GA 30310, USA. ' Proteomic Shared Resource, Oregon Health and Sciences University, 3181 SW Sam Jackson Park Rd, Portland, OR 97239, USA
Abstract: In a recent study on ischemic rodent brains, we quantitatively characterised and compared brain proteomes under ischemic-preconditioned or injured or tolerant conditions. We discovered an enriched presence of repressive transcriptional regulator proteins with essential roles as epigenetic regulators in ischemic-tolerant brains (Stapels et al., 2010). We further showed their robust, dynamic and differential changes under different ischemic conditions in brains and in cultured neuronal cells. In the present work, using neuronal cell cultures, we aimed to characterise the nascent proteome, the proteome that presents early when the cells receive an ischemic insult. These would be the proteomic changes of newly synthesised proteins. Identification of effectors of this phase of response to ischemia bears the best promise of identifying therapeutic targets for treating acute stroke when patients present to hospital. We compared these nascent proteomes across different ischemic conditions using bioinformatic tools.
Keywords: nascent proteomes; brain proteomes; ischemic injured brains; ischemic tolerant brains; neuronal cells; quantitative proteomics; epigenetic regulators; click chemistry; newly synthesised proteins; bioinformatics; computational biology; ischemic rodent brains; acute strokes; stroke treatment.
International Journal of Computational Biology and Drug Design, 2011 Vol.4 No.1, pp.40 - 55
Available online: 17 Feb 2011 *Full-text access for editors Access for subscribers Purchase this article Comment on this article