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The PIP2 binding mode of the C2 domains of rabphilin‐3A
Author(s) -
Montaville Pierre,
Coudevylle Nicolas,
Radhakrishnan Anand,
Leonov Andrei,
Zweckstetter Markus,
Becker Stefan
Publication year - 2008
Publication title -
protein science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.353
H-Index - 175
eISSN - 1469-896X
pISSN - 0961-8368
DOI - 10.1110/ps.073326608
Subject(s) - phosphatidylinositol , biophysics , binding domain , chemistry , c2 domain , inositol , binding site , domain (mathematical analysis) , plasma protein binding , protein domain , effector , crystallography , biochemistry , receptor , membrane , biology , signal transduction , mathematical analysis , mathematics , gene
Phosphatidylinositol‐4,5‐bisphosphate (PIP2) is a key player in the neurotransmitter release process. Rabphilin‐3A is a neuronal C2 domain tandem containing protein that is involved in this process. Both its C2 domains (C2A and C2B) are able to bind PIP2. The investigation of the interactions of the two C2 domains with the PIP2 headgroup IP3 (inositol‐1,4,5‐trisphosphate) by NMR showed that a well‐defined binding site can be described on the concave surface of each domain. The binding modes of the two domains are different. The binding of IP3 to the C2A domain is strongly enhanced by Ca 2+ and is characterized by a K D of 55 μM in the presence of a saturating concentration of Ca 2+ (5 mM). Reciprocally, the binding of IP3 increases the apparent Ca 2+ ‐binding affinity of the C2A domain in agreement with a Target‐Activated Messenger Affinity (TAMA) mechanism. The C2B domain binds IP3 in a Ca 2+ ‐independent fashion with low affinity. These different PIP2 headgroup recognition modes suggest that PIP2 is a target of the C2A domain of rabphilin‐3A while this phospholipid is an effector of the C2B domain.