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High affinity ATP/ADP analogues as new tools for studying CFTR gating
Author(s) -
Zhou Zhen,
Wang Xiaohui,
Li Min,
Sohma Yoshiro,
Zou Xiaoqin,
Hwang TzyhChang
Publication year - 2005
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2005.095083
Subject(s) - gating , chemistry , biophysics , biochemistry , microbiology and biotechnology , biology
Previous studies using non‐hydrolysable ATP analogues and hydrolysis‐deficient cystic fibrosis transmembrane conductance regulator (CFTR) mutants have indicated that ATP hydrolysis precedes channel closing. Our recent data suggest that ATP binding is also important in modulating the closing rate. This latter hypothesis predicts that ATP analogues with higher binding affinities should stabilize the open state more than ATP. Here we explore the possibility of using N 6 ‐modified ATP/ADP analogues as high‐affinity ligands for CFTR gating, since these analogues have been shown to be more potent than native ATP/ADP in other ATP‐binding proteins. Among the three N 6 ‐modified ATP analogues tested, N 6 ‐(2‐phenylethyl)‐ATP (P‐ATP) was the most potent, with a K ½ of 1.6 ± 0.4 μ m (>50‐fold more potent than ATP). The maximal open probability ( P o ) in the presence of P‐ATP was ∼30% higher than that of ATP, indicating that P‐ATP also has a higher efficacy than ATP. Single‐channel kinetic analysis showed that as [P‐ATP] was increased, the opening rate increased, whereas the closing rate decreased. The fact that these two kinetic parameters have different sensitivities to changes of [P‐ATP] suggests an involvement of two different ATP‐binding sites, a high‐affinity site modulating channel closing and a low affinity site controlling channel opening. The effect of P‐ATP on the stability of open states was more evident when ATP hydrolysis was abolished, either by mutating the nucleotide‐binding domain 2 (NBD2) Walker B glutamate (i.e. E1371) or by using the non‐hydrolysable ATP analogue AMP‐PNP. Similar strategies to develop nucleotide analogues with a modified adenine ring could be valuable for future studies of CFTR gating.