Stocker M, Pongs O, Hoth M, Heinemann S H, Stühmer W, Schröter K H, Ruppersberg J P
Ruhr-Universität Bochum, Lehrstuhl für Biochemie, F.R.G.
Proc Biol Sci. 1991 Aug 22;245(1313):101-7. doi: 10.1098/rspb.1991.0094.
Functionally significant properties of domains in the amino acid sequence of potassium (K+) channel-forming proteins have been investigated by constructing chimeric K+ channels. The N-terminal domain of ShA2 channels was responsible for the fast inactivation (IKA) and also determined a shift in the threshold of activation whereas the membrane domain determined the timecourse of slow inactivation. The binding site for dendrotoxin (DTX), but not for mast cell degranulating peptide (MCDP), is completely located on the loop between the membrane spanning segments S5 and S6 in RCK1 channels. A certain part of this region which has recently been designated as a narrow part of the pore was found to be not responsible for the differences in the single-channel current amplitude between RCK4 and RCK2 K+ channels. Interchange of the C-terminal domain did not influence activation or inactivation of the channels.
通过构建嵌合钾(K+)通道,研究了钾通道形成蛋白氨基酸序列中结构域的功能重要特性。ShA2通道的N端结构域负责快速失活(IKA),并且还决定了激活阈值的偏移,而膜结构域则决定了缓慢失活的时间进程。树突毒素(DTX)的结合位点完全位于RCK1通道中跨膜片段S5和S6之间的环上,而肥大细胞脱颗粒肽(MCDP)的结合位点则不在此。最近被指定为孔道狭窄部分的该区域的某一部分,被发现与RCK4和RCK2 K+通道之间单通道电流幅度的差异无关。C端结构域的互换不影响通道的激活或失活。