  
- 积分
- 0
- 威望
- 0
- 包包
- 3465
|
KONDOH/MACMILLAN
4 t- X7 B r1 V0 |
; X/ W! l3 h6 k4 L P4 R9 HA target of blood pressure–lowering drugs harbors the unexpected ability to release GPI-anchored proteins. Gen Kondoh (Kyoto University, Kyoto, Japan), Junji Takeda (Osaka University, Osaka, Japan), and colleagues reveal that this enzyme, ACE, is both a peptidase and GPIase in one multifunctional package.ACE's peptidase activity is well studied〞it cleaves and activates angiotensin, which up-regulates blood pressure through hormonal changes. But Kondoh did not expect to find ACE in his screen for proteins that release GPI-anchored proteins from the cell surface." @1 e t8 T" N! @/ c5 a: Y7 z6 P
2 t5 X$ k8 { PGPI deficiencies cause severe problems in fertility and development. GPI also links the prion protein to membranes. But the activities that release these linkages were not well-known. Now, Kondoh shows that a region of ACE distinct from its peptidase domain has this ability. Soluble prion protein protects against scrapie, so ACE, especially a peptidase-inactive form, may be a useful disease treatment.3 \* b2 S' D# A2 g( d$ G% ?
- _% c1 c. ~* iAs ACE was found in a mouse testicular preparation, the group examined sperm lacking the ACE GPIase activity. The mutant sperm were infertile and unable to release several GPI-linked proteins from their surface.! h) R& Q/ j3 R' c9 B3 w. @( _5 L$ @
$ f X0 l" E# F% i+ _) r$ `; ]8 TAnchored proteins were partly protected from ACE cleavage if they were in lipid rafts. By keeping GPI-linked fertilization factors in rafts, their release could be delayed until the raft disruption that occurs during capacitation.
/ l( q# G6 K( L& o' z! q; d5 [ v' I0 L& S- |* M
Reference:4 h1 q! I) G4 W7 N
$ i; o# z/ `9 y/ w5 U
Kondoh, G., et al. 2005. Nat. Med. doi:10.1038/nm1179(Sperm–egg binding (left) is lost when AC) |
|