Last year Zhang, Kuriyan and colleagues demonstrated that an asymmetric dimer interaction between EGF receptor kinase domains is a key element of receptor activation. They now show that a cellular protein that inhibits receptor activity targets this dimer interface, not only uncovering an important regulatory mechanism but also opening a new route to therapeutic kinase inhibition.
机构:
Univ Calif Santa Cruz, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA
Univ Calif Santa Cruz, Dept Cell Dev & Mol Biol, Santa Cruz, CA 95064 USAUniv Calif Santa Cruz, Ctr Mol Biol RNA, Santa Cruz, CA 95064 USA