OPINION Proteomic identification of multitasking proteins in unexpected locations complicates drug targeting

被引:113
作者
Butler, Georgina S. [1 ]
Overall, Christopher M.
机构
[1] Univ British Columbia, Ctr Blood Res, Dept Oral Biol & Med Sci, Vancouver, BC VT6 1Z3, Canada
基金
加拿大健康研究院;
关键词
TRANSFER-RNA SYNTHETASE; MATRIX-METALLOPROTEINASE INHIBITORS; TISSUE-GROWTH-FACTOR; NEUTROPHIL EXTRACELLULAR TRAPS; HSP90 MOLECULAR CHAPERONE; AUTOCRINE MOTILITY FACTOR; TAIL-BINDING PROTEIN-1; NUCLEAR EXPORT SIGNAL; GROUP BOX-1 PROTEIN; CANCER-CELLS;
D O I
10.1038/nrd2945
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Proteomics has revealed that many proteins are present in unexpected cellular locations. Moreover, it is increasingly recognized that proteins can translocate between intracellular and extracellular compartments in non-conventional ways. This increases gene pleiotrophy as the diverse functions of the protein that the gene encodes are dependent on the cellular location. Given that trafficking drug targets may exist in various forms-often with completely different functions-in multiple cellular compartments, careful interpretation of proteomics data is needed for an accurate understanding of gene function. This Perspective is intended to inspire the investigation of unusual protein localizations, rather than assuming that they are due to mislocalization or artefacts. Given a fair chance, proteomics could reveal novel and unforeseen biology with important ramifications for target validation in drug discovery.
引用
收藏
页码:935 / 948
页数:14
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