The N-terminus of KIR6.2 limits spontaneous bursting and modulates the ATP-inhibition of KATP channels

被引:70
作者
Babenko, AP [1 ]
Gonzalez, G [1 ]
Bryan, J [1 ]
机构
[1] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
关键词
D O I
10.1006/bbrc.1999.0172
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
K-ATP channels are heteromultimers of a sulfonylurea receptor SUR and K(IR)6.2 with the inward rectifier forming the pore which is regulated by SUR. We have examined the contributions of the cytoplasmic domains of K(IR)6.2 to control of spontaneous bursting and ATP-inhibition in human SUR1/K(IR)6.2 K-ATP channels. Truncations of the N-terminus of K(IR)6.2 nearly eliminate transitions to interburst closed states without affecting the open or intraburst closed states, thus producing SUR1/Delta NK(IR)6.2 channels with an extremely high open probability in the absence of nucleotides. These channels have a decrease apparent ATP-sensitivity which is consistent with the involvement of the N-terminus in a transition to an interburst closed state that preferentially binds inhibitory ATP. Mutations in both the N- and proximal C-termini of K(IR)6.2 can synergistically attenuate the ATP-inhibition. The results identify the N-terminus of K(IR)6.2 as a determinant of the interburst kinetics of K-ATP channels and suggest that the two cytoplasmic domains of K(IR)6.2 participate in ATP-inhibitory gating through distinct mechanisms. (C) 1999 Academic Press.
引用
收藏
页码:231 / 238
页数:8
相关论文
共 32 条
  • [21] Three-dimensional architecture and gating mechanism of a K+ channel studied by EPR spectroscopy
    Perozo, E
    Cortes, DM
    Cuello, LG
    [J]. NATURE STRUCTURAL BIOLOGY, 1998, 5 (06) : 459 - 469
  • [22] SCHWAPPACH B, 1998, 2 INT C ATP SENS POT, P232
  • [23] Control of rectification and gating of cloned K-ATP channels by the Kir6.2 subunit
    Shyng, SL
    Ferrigni, T
    Nichols, CG
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1997, 110 (02) : 141 - 153
  • [24] Regulation of K-ATP channel activity by diazoxide and MgADP - Distinct functions of the two nucleotide binding folds of the sulfonylurea receptor
    Shyng, SL
    Ferrigni, T
    Nichols, CG
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1997, 110 (06) : 643 - 654
  • [25] Cytoplasmic terminus domains of Kir6.x confer different nucleotide-dependent gating on the ATP-sensitive K+ channel
    Takano, M
    Xie, LH
    Otani, H
    Horie, M
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1998, 512 (02): : 395 - 406
  • [26] THE ATP-SENSITIVE K+ CHANNEL
    TAKANO, M
    NOMA, A
    [J]. PROGRESS IN NEUROBIOLOGY, 1993, 41 (01) : 21 - 30
  • [27] Mechanism of ATP-sensitive K channel inhibition by sulfhydryl modification
    Trapp, S
    Tucker, SJ
    Ashcroft, FM
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1998, 112 (03) : 325 - 332
  • [28] Molecular analysis of ATP-sensitive K channel gating and implications for channel inhibition by ATP
    Trapp, S
    Proks, P
    Tucker, SJ
    Ashcroft, FM
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1998, 112 (03) : 333 - 349
  • [29] INWARD-RECTIFYING CHANNELS IN ISOLATED PATCHES OF THE HEART CELL-MEMBRANE - ATP-DEPENDENCE AND COMPARISON WITH CELL-ATTACHED PATCHES
    TRUBE, G
    HESCHELER, J
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1984, 401 (02): : 178 - 184
  • [30] Molecular determinants of KATP channel inhibition by ATP
    Tucker, SJ
    Gribble, FM
    Proks, P
    Trapp, S
    Ryder, TJ
    Haug, T
    Reimann, F
    Ashcroft, FM
    [J]. EMBO JOURNAL, 1998, 17 (12) : 3290 - 3296