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10.1016/j.bpj.2014.12.055

http://scihub22266oqcxt.onion/10.1016/j.bpj.2014.12.055
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C4375528!4375528!25809253
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suck abstract from ncbi


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pmid25809253      Biophys+J 2015 ; 108 (6): 1400-13
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  • NS1643 Interacts around L529 of hERG to Alter Voltage Sensor Movement on the Path to Activation #MMPMID25809253
  • Guo J; Cheng Y; Lees-Miller J; Perissinotti L; Claydon T; Hull C; Thouta S; Roach D; Durdagi S; Noskov S; Duff H
  • Biophys J 2015[Mar]; 108 (6): 1400-13 PMID25809253show ga
  • Activators of hERG1 such as NS1643 are being developed for congenital/acquired long QT syndrome. Previous studies identify the neighborhood of L529 around the voltage-sensor as a putative interacting site for NS1643. With NS1643, the V1/2 of activation of L529I (?34 ± 4 mV) is similar to wild-type (WT) (?37 ± 3 mV; P > 0.05). WT and L529I showed no difference in the slope factor in the absence of NS1643 (8 ± 0 vs. 9 ± 0) but showed a difference in the presence of NS1643 (9 ± 0.3 vs. 22 ± 1; P < 0.01). Voltage-clamp-fluorimetry studies also indicated that in L529I, NS1643 reduces the voltage-sensitivity of S4 movement. To further assess mechanism of NS1643 action, mutations were made in this neighborhood. NS1643 shifts the V1/2 of activation of both K525C and K525C/L529I to hyperpolarized potentials (?131 ± 4 mV for K525C and ?120 ± 21 mV for K525C/L529I). Both K525C and K525C/K529I had similar slope factors in the absence of NS1643 (18 ± 2 vs. 34 ± 5, respectively) but with NS1643, the slope factor of K525C/L529I increased from 34 ± 5 to 71 ± 10 (P < 0.01) whereas for K525C the slope factor did not change (18 ± 2 at baseline and 16 ± 2 for NS1643). At baseline, K525R had a slope factor similar to WT (9 vs. 8) but in the presence of NS1643, the slope factor of K525R was increased to 24 ± 4 vs. 9 ± 0 mV for WT (P < 0.01). Molecular modeling indicates that L529I induces a kink in the S4 voltage-sensor helix, altering a salt-bridge involving K525. Moreover, docking studies indicate that NS1643 binds to the kinked structure induced by the mutation with a higher affinity. Combining biophysical, computational, and electrophysiological evidence, a mechanistic principle governing the action of some activators of hERG1 channels is proposed.
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