Genome to Kinome: Species-Specific Peptide Arrays for Kinome Analysis

被引:65
作者
Jalal, Shakiba [1 ,2 ]
Arsenault, Ryan [1 ,2 ]
Potter, Andrew A. [1 ]
Babiuk, Lorne A. [3 ]
Griebel, Philip J. [1 ]
Napper, Scott [1 ]
机构
[1] Univ Saskatchewan, Vaccine & Infect Dis Org, Saskatoon, SK S7N 5E3, Canada
[2] Univ Saskatchewan, Dept Biochem, Saskatoon, SK S7N 5E5, Canada
[3] Univ Alberta, Edmonton, AB T6G 2J9, Canada
关键词
DEPENDENT PROTEIN-KINASE; SUBSTRATE-SPECIFICITY; ANIMAL-MODELS; PHOSPHORYLATION; PHOSPHOPROTEOME; LIPOPOLYSACCHARIDE; MOUSE; CHIPS; SITE;
D O I
10.1126/scisignal.254pl1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tools for conducting high-throughput kinome analysis do not exist for many species. For example, two commonly used techniques for monitoring phosphorylation events are phosphorylation-specific antibodies and peptide arrays. The majority of phosphorylation-specific antibodies are for human or mouse targets, and the construction of peptide arrays relies on information from phosphorylation databases, which are similarly biased toward human and mouse data. This is a substantial obstacle because many species other than mouse represent important biological models. On the basis of the observation that phosphorylation events are often conserved across species with respect to their relative positioning within proteins and their biological function, we demonstrate that it is possible to predict the sequence contexts of phosphorylation events in other species for the production of peptide arrays for kinome analysis. Through this approach, genomic information can be rapidly used to create inexpensive, customizable, species-specific peptide arrays for high-throughput kinome analysis. We anticipate that these arrays will be valuable for investigating the conservation of biological responses across species, validating animal models of disease, and translating research to clinical applications
引用
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页数:11
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