Use of ProteoMiner in Vetenery Research

sis of interacting partners of different proteins that are presented in TERMs [2]. This was accomplished by “pull-down” techniques and high-throughput protein trometry. For this end, synthetic biotinylated peptides spanning the C-terminal cytoplasmic end of these proteins were incubated with extracts from lymphoblast cell models, and then captured using Streptavidin-sepharose microbeads. Proteins interacting with the peptide baits were subjected to digestion and the resulting peptides systematically analyzed by HPLC-linear ion trap MS/MS mass spectrometry. Proteins from more