Collapsin response mediator protein-2 is a calmodulin-binding protein

被引:25
|
作者
Zhang, Z. [1 ]
Majava, V. [2 ]
Greffier, A. [2 ]
Hayes, R. L. [1 ,3 ]
Kursula, P. [2 ]
Wang, K. K. W. [1 ,4 ]
机构
[1] Banyan Biomarkers Inc, Ctr Innovat Res, Alachua, FL 32615 USA
[2] Univ Oulu, Dept Biochem, Oulu, Finland
[3] Univ Florida, McKnight Brain Inst, Dept Anesthesiol, Gainesville, FL USA
[4] Univ Florida, McKnight Brain Inst, Dept Psychiat, Gainesville, FL USA
基金
芬兰科学院;
关键词
CRMP-2; proteolysis; calmodulin; calmodulin-binding protein; oligomerization; TRAUMATIC BRAIN-INJURY; MYELIN BASIC-PROTEIN; MOUSE-BRAIN; NEURONAL POLARITY; CALPAIN; CLEAVAGE; CRMP-2; PROTEOLYSIS; DYNAMICS; GROWTH;
D O I
10.1007/s00018-008-8362-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Collapsin response mediator protein-2 (CRMP-2) plays a crucial role in axonal guidance and neurite outgrowth during neural development and regeneration. We have studied the interaction between calmodulin (CaM) and CRMP-2 and how Ca(2+)/CaM binding modulates the biological functions of CRMP-2. We have shown that CRMP-2 binds to CaM directly in a Ca(2+)-dependent manner. The CaM binding site of CRMP-2 is proposed to reside in the last helix of the folded domain, and in line with this, a synthesized peptide representing this helix bound to CaM. In addition, CaM binding inhibits a homotetrameric assembly of CRMP-2 and attenuates calpainmediated CRMP-2 proteolysis. Furthermore, a CaM antagonist reduces the number and length of process induced by CRMP-2 overexpression in HEK293 cells. Take together, our data suggest that CRMP-2 is a novel CaM-binding protein and that CaM binding may play an important role in regulating CRMP-2 functions.
引用
收藏
页码:526 / 536
页数:11
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