TITLE

PROTEOMIC SOLUTIONS FOR ANALYTICAL CHALLENGES ASSOCIATED WITH ALCOHOL RESEARCH

AUTHOR(S)
MacCoss, Michael J.; Wu, Christine C.
PUB. DATE
September 2008
SOURCE
Alcohol Research & Health;2008, Vol. 31 Issue 3, p251
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Alcohol addiction is a complex disease with both hereditary and environmental influences. Because molecular determinants contributing to this phenotype are difficult to study in humans, numerous rodent models and conditioning paradigms have provided powerful tools to study the molecular complexities underlying these behavioral phenotypes (Crabbe 2002). In particular, specifically bred rodents (i.e., selected lines and inbred strains) that differ in voluntary alcohol drinking represent valuable tools to dissect the genetic components of alcoholism. However, because each model has distinct advantages, a combined comparison across datasets of different models for common changes in gene expression would provide more statistical power to detect reliable changes as opposed to the analysis of any one model. Indeed, meta-analyses of diverse gene expression datasets were recently performed to uncover genes related to the predisposition for a high alcohol intake. This large endeavor resulted in the identification of 3,800 unique genes that significantly and consistently changed between all included mouse lines and strains (Mulligan et al. 2006). Similar experiments also are crucial at the protein level. However, these analyses are not yet possible. Proteins do not conform to any one uniform sample preparation method and/or biochemical analysis. They display a broad range of physical and chemical properties (e.g., molecular weight or hydrophobicity) and are expressed over a very large dynamic range (up to 8 orders of magnitude) (Anderson 2005; Ghaemmaghami et al. 2003). Further complicating global proteomic comparisons are the added considerations that proteins often undergo extensive covalent modifications and that protein functions often are regulated by complex protein-protein interactions and the specific location of the proteins in the cell (i.e., their subcellular localization) (Grant and Wu 2007). Furthermore, because the number of biological replicates involved in behavioral analyses typically is high, robust high-throughput proteomic platforms will be required to handle the multitude of protein samples that can potentially result from the various brain regions for the numerous animal models and paradigms. Finally, these effects often are monitored over time courses, again inflating the total number of samples that need to be analyzed and compared. This article summarizes some general strategies for large-scale, high-throughput protein analyses and describes two new proteomic strategies that appear promising for future studies in this field.
ACCESSION #
35876020

 

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