作者: Martin Wieske , Rainer Benndorf , Joachim Behlke , Rudolf Dölling , Gerlinde Grelle
DOI: 10.1046/J.1432-1327.2001.02082.X
关键词: Peptide 、 Actin-binding protein 、 Polymerization 、 Cell biology 、 Phosphorylation 、 Chemistry 、 Serine 、 In vivo 、 Inhibitory postsynaptic potential 、 Actin 、 Biochemistry
摘要: N-terminally extended peptide 11 at serine residues known to be phosphorylated in vivo resulted decline of their inhibitory activity. Interestingly, peptides derived from the homologous sequence murine aB-crystallin showed same behaviour. The results suggest that both HSP25 and have potential inhibit actin polymerization this activity is regulated by phosphorylation.