KCNMB1 regulates surface expression of a voltage and Ca2+-activated K+ channel via endocytic trafficking signals

[1]  E. Stefani,et al.  MaxiK channel partners: physiological impact , 2006, The Journal of physiology.

[2]  O. McManus,et al.  Role of the C-terminus of the high-conductance calcium-activated potassium channel in channel structure and function. , 2005, Biochemistry.

[3]  A. Morielli,et al.  Endocytosis as a mechanism for tyrosine kinase-dependent suppression of a voltage-gated potassium channel. , 2004, Molecular biology of the cell.

[4]  E. Stefani,et al.  Functional and molecular evidence of MaxiK channel β1 subunit decrease with coronary artery ageing in the rat , 2004, The Journal of physiology.

[5]  E. Stefani,et al.  An endoplasmic reticulum trafficking signal prevents surface expression of a voltage- and Ca2+-activated K+ channel splice variant. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[6]  J F Storm,et al.  Cerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel deficiency. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[7]  E. Asante-Appiah,et al.  Protein Tyrosine Phosphatase-1B Dephosphorylation of the Insulin Receptor Occurs in a Perinuclear Endosome Compartment in Human Embryonic Kidney 293 Cells* , 2004, Journal of Biological Chemistry.

[8]  D. McDonald,et al.  Upon thyrotropin binding the thyrotropin receptor is internalized and localized to endosome. , 2004, Endocrinology.

[9]  J. Bonifacino,et al.  Signals for sorting of transmembrane proteins to endosomes and lysosomes. , 2003, Annual review of biochemistry.

[10]  L. Santana,et al.  Downregulation of the BK Channel &bgr;1 Subunit in Genetic Hypertension , 2003, Circulation research.

[11]  A. Bonev,et al.  Modulation of the molecular composition of large conductance, Ca(2+) activated K(+) channels in vascular smooth muscle during hypertension. , 2003, The Journal of clinical investigation.

[12]  W. Guggino,et al.  The Cytoplasmic Tail of Large Conductance, Voltage- and Ca2+-activated K+ (MaxiK) Channel Is Necessary for Its Cell Surface Expression* , 2003, The Journal of Biological Chemistry.

[13]  R. Aldrich,et al.  β1‐Subunit of the Ca2+‐activated K+ channel regulates contractile activity of mouse urinary bladder smooth muscle , 2001 .

[14]  K. Roche,et al.  Molecular determinants of NMDA receptor internalization , 2001, Nature Neuroscience.

[15]  E. Stefani,et al.  A Novel MaxiK Splice Variant Exhibits Dominant-negative Properties for Surface Expression* , 2001, The Journal of Biological Chemistry.

[16]  G. Lukács,et al.  Multiple endocytic signals in the C-terminal tail of the cystic fibrosis transmembrane conductance regulator. , 2001, The Biochemical journal.

[17]  O. Pongs,et al.  Mice With Disrupted BK Channel &bgr;1 Subunit Gene Feature Abnormal Ca2+ Spark/STOC Coupling and Elevated Blood Pressure , 2000, Circulation research.

[18]  R. Latorre,et al.  Apical sorting of a voltage- and Ca2+-activated K+ channel alpha -subunit in Madin-Darby canine kidney cells is independent of N-glycosylation. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[19]  R. Aldrich,et al.  Vasoregulation by the β1 subunit of the calcium-activated potassium channel , 2000, Nature.

[20]  V. Uebele,et al.  Cloning and Functional Expression of Two Families of β-Subunits of the Large Conductance Calcium-activated K+ Channel* , 2000, The Journal of Biological Chemistry.

[21]  P. Distefano,et al.  A Novel Nervous System β Subunit that Downregulates Human Large Conductance Calcium-Dependent Potassium Channels , 2000, The Journal of Neuroscience.

[22]  L. Toro,et al.  A neuronal beta subunit (KCNMB4) makes the large conductance, voltage- and Ca2+-activated K+ channel resistant to charybdotoxin and iberiotoxin. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[23]  R. Aldrich,et al.  Cloning and Functional Characterization of Novel Large Conductance Calcium-activated Potassium Channel β Subunits, hKCNMB3 and hKCNMB4* , 2000, The Journal of Biological Chemistry.

[24]  H. Mellor,et al.  Regulation of endocytic traffic by rho family GTPases. , 2000, Trends in cell biology.

[25]  J. Bonifacino,et al.  Utilization of the indirect lysosome targeting pathway by lysosome-associated membrane proteins (LAMPs) is influenced largely by the C-terminal residue of their GYXXphi targeting signals. , 1999, Journal of cell science.

[26]  E. Stefani,et al.  Hormonal control of protein expression and mRNA levels of the MaxiK channel α subunit in myometrium , 1999, FEBS letters.

[27]  C. Lingle,et al.  Molecular Basis for the Inactivation of Ca2+- and Voltage-Dependent BK Channels in Adrenal Chromaffin Cells and Rat Insulinoma Tumor Cells , 1999, The Journal of Neuroscience.

[28]  A. Koschak,et al.  High-conductance calcium-activated potassium channels in rat brain: pharmacology, distribution, and subunit composition. , 1999, Biochemistry.

[29]  L. Toro,et al.  Molecular basis of fast inactivation in voltage and Ca2+-activated K+ channels: a transmembrane beta-subunit homolog. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[30]  J. Bonifacino,et al.  The Medium Subunits of Adaptor Complexes Recognize Distinct but Overlapping Sets of Tyrosine-based Sorting Signals* , 1998, The Journal of Biological Chemistry.

[31]  C. Nobes,et al.  PRK1 Is Targeted to Endosomes by the Small GTPase, RhoB* , 1998, The Journal of Biological Chemistry.

[32]  L. Toro,et al.  Large conductance voltage- and calcium-dependent K+ channel, a distinct member of voltage-dependent ion channels with seven N-terminal transmembrane segments (S0-S6), an extracellular N terminus, and an intracellular (S9-S10) C terminus. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[33]  L. Toro,et al.  A calcium switch for the functional coupling between α (hslo) and β subunits (K V , Ca β) of maxi K channels , 1996 .

[34]  O. Pongs,et al.  Distribution of high-conductance Ca(2+)-activated K+ channels in rat brain: targeting to axons and nerve terminals , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[35]  J. Warmke,et al.  Characterization of Tissue-expressed α Subunits of the High Conductance Ca2+-activated K+ Channel (*) , 1995, The Journal of Biological Chemistry.

[36]  L. Pallanck,et al.  Functional role of the β subunit of high conductance calcium-activated potassium channels , 1995, Neuron.

[37]  O. Bakke,et al.  An LI and ML motif in the cytoplasmic tail of the MHC-associated invariant chain mediate rapid internalization. , 1994, Journal of cell science.

[38]  Xin-Yun Huang,et al.  Tyrosine kinase-dependent suppression of a potassium channel by the G protein-coupled m1 muscarinic acetylcholine receptor , 1993, Cell.

[39]  R. Klausner,et al.  A novel di-leucine motif and a tyrosine-based motif independently mediate lysosomal targeting and endocytosis of CD3 chains , 1992, Cell.

[40]  M. Roth,et al.  Characteristics of the tyrosine recognition signal for internalization of transmembrane surface glycoproteins , 1990, The Journal of cell biology.

[41]  M. Fukuda,et al.  Accumulation of membrane glycoproteins in lysosomes requires a tyrosine residue at a particular position in the cytoplasmic tail , 1990, The Journal of cell biology.

[42]  S. Archer,et al.  Potassium Channels in Cardiovascular Biology , 2001, Springer US.

[43]  R. Latorre,et al.  Characterization of and modulation by a beta-subunit of a human maxi KCa channel cloned from myometrium. , 1995, Receptors & channels.

[44]  S. Heinemann,et al.  Cloned glutamate receptors. , 1994, Annual review of neuroscience.

[45]  M. Robinson,et al.  Clathrin, adaptors, and sorting. , 1990, Annual review of cell biology.