作者: Fabrice Agou , Michel Véron
DOI: 10.1007/978-1-4939-2425-7_26
关键词: In vitro 、 Nucleoside-diphosphate kinase 、 Biophysics 、 Context (language use) 、 Signal transduction 、 In vivo 、 Chemistry 、 Random hexamer 、 Protein oligomerization 、 Protein structure
摘要: In the cell, homo- and heteroassociations of polypeptide chains evolve take place within subcellular compartments that are crowded with many other cellular macromolecules. vivo chemical cross-linking proteins is a powerful method to examine changes in protein oligomerization protein-protein interactions upon events such as signal transduction. This chapter intended provide guide selection cell-membrane-permeable cross-linkers, optimization conditions, identification specific cross-links context where frequency random collisions high. By combining chemoselectivity homo-bifunctional cross-linker length its spacer arm knowledge on structure, we show selective can be introduced specifically either dimer or hexamer form same vitro well vivo, using human type B nucleoside diphosphate kinase model.