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Comprehensive profiling of CTP-binding proteins using a biotinylated CTP affinity probe
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作者 Mengting Pa Yunming Liu +3 位作者 Xiaofang Zheng Meijuan Zhou Changjun You Xiaoxia Dai 《Chinese Chemical Letters》 SCIE CAS CSCD 2021年第11期3479-3482,共4页
Recent studies have shown that CTP may act as a ligand to regulate the activity of its target proteins in many biological processes.However,proteome-wide identification of CTP-binding proteins remains challenging.Here... Recent studies have shown that CTP may act as a ligand to regulate the activity of its target proteins in many biological processes.However,proteome-wide identification of CTP-binding proteins remains challenging.Here,we employed a biotinylated CTP affinity probe coupled with stable isotope labeling by amino acids in cell culture(SILAC)-based quantitative proteomics approach to capture,identify and quantify CTP-binding proteins in human cells.By performing two types of competitive SILAC experiments with high vs.low concentrations of CTP probe(100 vs.10µmol/L)or with CTP probe in the presence of free CTP,we identified 90 potential CTP-binding proteins which are involved in a variety of biological processes,including protein folding,nucleotide binding and cell-cell adhesion.Together,we developed a chemical proteomic method for uncovering the CTP-binding proteins in human cells,which could be widely applicable for profiling CTP-binding proteins in other biological samples. 展开更多
关键词 ctp-binding proteins CTP affinity probe Mass spectrometry SILAC Quantitative proteomics
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