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J Gen Physiol
2001 Oct 01;1184:341-53. doi: 10.1085/jgp.118.4.341.
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Mutations within the P-loop of Kir6.2 modulate the intraburst kinetics of the ATP-sensitive potassium channel.
Proks P
,
Capener CE
,
Jones P
,
Ashcroft FM
.
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The ATP-sensitive potassium (K(ATP)) channel exhibits spontaneous bursts of rapid openings, which are separated by long closed intervals. Previous studies have shown that mutations at the internal mouth of the pore-forming (Kir6.2) subunit of this channel affect the burst duration and the long interburst closings, but do not alter the fast intraburst kinetics. In this study, we have investigated the nature of the intraburst kinetics by using recombinant Kir6.2/SUR1 K(ATP) channels heterologously expressed in Xenopus oocytes. Single-channel currents were studied in inside-out membrane patches. Mutations within the pore loop of Kir6.2 (V127T, G135F, and M137C) dramatically affected the mean open time (tau(o)) and the short closed time (tauC1) within a burst, and the number of openings per burst, but did not alter the burst duration, the interburst closed time, or the channel open probability. Thus, the V127T and M137C mutations produced longer tau(o), shorter tauC1, and fewer openings per burst, whereas the G135F mutation had the opposite effect. All three mutations also reduced the single-channel conductance: from 70 pS for the wild-type channel to 62 pS (G135F), 50 pS (M137C), and 38 pS (V127T). These results are consistent with the idea that the K(ATP) channel possesses a gate that governs the intraburst kinetics, which lies close to the selectivity filter. This gate appears to be able to operate independently of that which regulates the long interburst closings.
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11585848
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Figure 1. (A) Single-channel currents recorded at â130 mV from two different inside-out patches excised from an oocyte expressing Kir6.2 and SUR1. Currents were recorded in the presence of 10 mM (above) or 140 mM (below) symmetrical K+ solutions. The dashed line indicates the zero current level.
Figure 2. (A) Single-channel currents recorded at â60 mV from an inside-out patch excised from an oocyte expressing Kir6.2/SUR1, Kir1.1, or Kir2.1, as indicated. Currents were recorded in a symmetrical 140-mM solution. The dashed line indicates the zero current level. (B) Sequence of the pore loop of Kir6.2 compared with that of some other types of K+ channel. Arrows indicate the mutated residues.
Figure 3. (A) Single-channel currents (left) and corresponding amplitude histograms (right) recorded at â60 mV from an inside-out patch excised from an oocyte expressing the channel indicated. The dashed line indicates the zero current level. (B) Mean current-voltage relations measured for Kir6.2/SUR1 (O, n = 3), Kir6.2-V127T/SUR1 (âª, n = 3), Kir6.2-G135F/SUR1 (â¢, n = 3), and Kir6.2-M137C/SUR1 (â¡, n = 3) channels in symmetrical 140-mM K+. The lines are fitted through the data points using a spline function.
Figure 4. (A) Open time distributions measured at â60 mV for wild-type (WT) and mutant Kir6.2/SUR1 channels, as indicated. The lines are fitted to either one exponential (WT, G135F) or the sum of two exponentials (V127T and M137C) with the time constants indicated. (B) Closed time distributions measured at â60 mV for wild-type (WT) and mutant Kir6.2/SUR1 channels, as indicated. The lines are fitted to the sum of three exponentials with the time constants indicated.
Figure 5. (A) Single-channel currents recorded at â60 mV from an inside-out patch excised from oocytes expressing SUR1 and either Kir6.2, Kir6.2-V127T, or Kir6.2-V127T + F133Y. The dashed line indicates the zero current level. (B) Mean current-voltage relations measured for Kir6.2/SUR1 (â, n = 3), Kir6.2-V127T/SUR1 (âª, n = 3), or Kir6.2-V127T+F133Y/SUR1 (â¢, n = 3). The lines are fitted through the data points using a spline function.
Figure 6. Mean kinetic parameters for wild-type and mutant channels measured at â60 mV (n = 5). *P < 0.05.
Figure 7. (A) Molecular model of the structure of the pore of Kir6.2 based on that of KcsA. The positions of the putative fast and slow gates are indicated. (red) M1-helix, (green) P-helix and filter, and (blue) M2-helix. (B) Molecular model of the selectivity filter of Kir6.2 based on that of KcsA. Residues that affect gating when mutated are highlighted ([magenta] V127, [yellow] G135; and [cyan] M137).
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