A Synthetic Polyphosphoinositide Headgroup Surrogate in Complex with SHIP2 Provides a Rationale for Drug Discovery

作者：Mills Stephen J; Persson Camilla; Cozier Gyles; Thomas Mark P; Tresaugues Lionel; Erneux Christophe; Riley Andrew M; Nordlund Par; Potter Barry V L^*

来源：ACS Chemical Biology, 2012, 7(5): 822-828.

DOI：10.1021/cb200494d

Phosphoinositides regulate many cellular processes, and cellular levels are controlled by kinases and phosphatases. SHIP2 (SH2 (Src homology 2)-domain-containing inositol-phosphatase-2) plays a critical role in phosphoinositide signaling, cleaving the 5-phosphate from phosphatidylinositol 3,4,5-trisphosphate. SHIP2 is thought to be involved in type-2 diabetes and obesity, conditions that could therefore be open to pharmacological modulation of the enzyme. However, rational design of SHIP2 inhibitors has been limited by the absence of a high-resolution structure. Here, we present a 2.1 angstrom resolution crystal structure of the phosphatase domain of SHIP2 bound to the synthetic ligand biphenyl 2,3%26apos;,4,5%26apos;,6-pentakisphosphate (BiPh(2,3%26apos;,4,5%26apos;,6)P-5). BiPh(2,3%26apos;,4,5%26apos;,6)P-5 is not a SHIP2 substrate but inhibits Ins(1,3,4,5)P-4 hydrolysis with an IC50 of 24.8 +/- 3.0 mu M, (K-m for Ins(1,3,4,5)P-4 is 215 +/- 28 mu M). Molecular dynamics simulations suggest that when BiPh(2,3%26apos;,4,5%26apos;,6)P-5 binds to SHIP2, a flexible loop folds over and encloses the ligand. Compounds targeting such a closed conformation might therefore deliver SHIP2-specific drugs.

• 出版日期2012-5
• 单位南阳理工学院