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  1. Tripartite interactions of PKA catalytic subunit and C-terminal domains of cardiac Ca 2+ channel modulate its β-adrenergic regulation

    This article has 21 authors:
    1. Shimrit Oz
    2. Tom Sharon
    3. Suraj Subramaniam
    4. Tamara Pallien
    5. Moshe Katz
    6. Vladimir Tsemakhovich
    7. Debi Ranjan Tripathy
    8. Giorgia Sasson
    9. Orna Chomsky-Hecht
    10. Leonid Vysochek
    11. Maike Schulz
    12. Claudia Fecher-Trost
    13. Kerstin Zühlke
    14. Daniela Bertinetti
    15. Friedrich W. Herberg
    16. Tal Keren-Raifman
    17. Veit Flockerzi
    18. Joel A. Hirsch
    19. Enno Klussmann
    20. Sharon Weiss
    21. Nathan Dascal
    This article has no evaluationsAppears in 1 listLatest version
  2. Allosteric competition and inhibition in AMPA receptors

    This article has 7 authors:
    1. W. Dylan Hale
    2. Alejandra Montaño Romero
    3. Cuauhtemoc U. Gonzalez
    4. Vasanthi Jayaraman
    5. Albert Y. Lau
    6. Richard L. Huganir
    7. Edward C. Twomey
    This article has no evaluationsAppears in 1 listLatest version
  3. Allosteric modulation of the CXCR4:CXCL12 axis by targeting receptor nanoclustering via the TMV-TMVI domain

    This article has 25 authors:
    1. Eva M García-Cuesta
    2. Pablo Martínez
    3. Karthik Selvaraju
    4. Gabriel Ulltjärn
    5. Adrián Miguel Gómez Pozo
    6. Gianluca D'Agostino
    7. Sofia Gardeta
    8. Adriana Quijada-Freire
    9. Patricia Blanco Gabella
    10. Carlos Roca
    11. Daniel del Hoyo
    12. Rodrigo Jiménez-Saiz
    13. Alfonso García-Rubia
    14. Blanca Soler Palacios
    15. Pilar Lucas
    16. Rosa Ayala-Bueno
    17. Noelia Santander Acerete
    18. Yolanda Carrasco
    19. Carlos Oscar Sorzano
    20. Ana Martinez
    21. Nuria E Campillo
    22. Lasse D Jensen
    23. Jose Miguel Rodriguez Frade
    24. César Santiago
    25. Mario Mellado
    This article has been curated by 1 group:
    • Curated by eLife

      eLife assessment

      This is an important study that describes an elegant modelling driven approach to design of allosteric antagonists for CXCR4 that have a selective effect on receptor nanocluster formation, cell polarisation and chemotaxis, but spare binding of CXCL12 to the receptor and inhibition of adenylate cyclase. This enables selective targeting of processes dependent upon cell polarisation and chemotaxis without impacting signalling effects and may avoid some of the toxicity associated with antagonists that target CXCL12 binding and thus block all CXCR4 signalling. The revised manuscript offers convincing evidence to support the claims. The modelling work is better described and additional data has been presented that better illustrates the unique features of the new antagonist. The in vivo studies in the zebrafish model open a path to studies in mammalian models.

    Reviewed by eLife

    This article has 7 evaluationsAppears in 2 listsLatest version Latest activity
  4. The Sec61/TRAP Translocon Scrambles Lipids

    This article has 5 authors:
    1. Matti Javanainen
    2. Sudeep Karki
    3. Dale Tranter
    4. Denys Biriukov
    5. Ville O. Paavilainen
    This article has no evaluationsAppears in 1 listLatest version