Branka Radic-Sarikas , Uwe Rix , Alexey Stukalov , Manuela Gridling , André C. Müller , Jacques Colinge , Giulio Superti-Furga , Keiryn L. Bennett
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引用次数: 2
Abstract
Gel-free liquid chromatography mass spectrometry coupled to chemical proteomics is a powerful approach for characterizing cellular target profiles of small molecules. We have previously described a fast and efficient elution protocol; however, altered target profiles were observed. We hypothesised that elution conditions critically impact the effectiveness of disrupting drug-protein interactions. Thus, a number of elution conditions were systematically assessed with the aim of improving the recovery of all classes of proteins whilst maintaining compatibility with immunoblotting procedures. A double elution with formic acid combined with urea emerged as the most efficient and generically applicable elution method for chemical proteomics
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