Abstract
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Journal of Biological Chemistry |
| Vol/bind | 281 |
| Udgave nummer | 25 |
| Sider (fra-til) | 17337-46 |
| Antal sider | 9 |
| ISSN | 0021-9258 |
| DOI | |
| Status | Udgivet - 2006 |
Bibliografisk note
Keywords: Amino Acid Sequence; Animals; COS Cells; Cattle; Cell Membrane; Cercopithecus aethiops; Copper; Metals; Molecular Conformation; Molecular Sequence Data; Protein Binding; Receptors, Adrenergic, beta-2; Rhodopsin; ZincAdgang til dokumentet
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I: Journal of Biological Chemistry, Bind 281, Nr. 25, 2006, s. 17337-46.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
}
TY - JOUR
T1 - Metal ion site engineering indicates a global toggle switch model for seven-transmembrane receptor activation
AU - Elling, Christian E
AU - Frimurer, Thomas M
AU - Gerlach, Lars-Ole
AU - Jorgensen, Rasmus
AU - Holst, Birgitte
AU - Schwartz, Thue W
N1 - Keywords: Amino Acid Sequence; Animals; COS Cells; Cattle; Cell Membrane; Cercopithecus aethiops; Copper; Metals; Molecular Conformation; Molecular Sequence Data; Protein Binding; Receptors, Adrenergic, beta-2; Rhodopsin; Zinc
PY - 2006
Y1 - 2006
N2 - Much evidence indicates that, during activation of seven-transmembrane (7TM) receptors, the intracellular segments of the transmembrane helices (TMs) move apart with large amplitude, rigid body movements of especially TM-VI and TM-VII. In this study, AspIII:08 (Asp113), the anchor point for monoamine binding in TM-III, was used as the starting point to engineer activating metal ion sites between the extracellular segments of the beta2-adrenergic receptor. Cu(II) and Zn(II) alone and in complex with aromatic chelators acted as potent (EC50 decreased to 0.5 microm) and efficacious agonists in sites constructed between positions III:08 (Asp or His), VI:16 (preferentially Cys), and/or VII:06 (preferentially Cys). In molecular models built over the backbone conformation of the inactive rhodopsin structure, the heavy atoms that coordinate the metal ion were located too far away from each other to form high affinity metal ion sites in both the bidentate and potential tridentate settings. This indicates that the residues involved in the main ligand-binding pocket will have to move closer to each other during receptor activation. On the basis of the distance constraints from these activating metal ion sites, we propose a global toggle switch mechanism for 7TM receptor activation in which inward movement of the extracellular segments of especially TM-VI and, to some extent, TM-VII is coupled to the well established outward movement of the intracellular segments of these helices. We suggest that the pivots for these vertical seesaw movements are the highly conserved proline bends of the involved helices.
AB - Much evidence indicates that, during activation of seven-transmembrane (7TM) receptors, the intracellular segments of the transmembrane helices (TMs) move apart with large amplitude, rigid body movements of especially TM-VI and TM-VII. In this study, AspIII:08 (Asp113), the anchor point for monoamine binding in TM-III, was used as the starting point to engineer activating metal ion sites between the extracellular segments of the beta2-adrenergic receptor. Cu(II) and Zn(II) alone and in complex with aromatic chelators acted as potent (EC50 decreased to 0.5 microm) and efficacious agonists in sites constructed between positions III:08 (Asp or His), VI:16 (preferentially Cys), and/or VII:06 (preferentially Cys). In molecular models built over the backbone conformation of the inactive rhodopsin structure, the heavy atoms that coordinate the metal ion were located too far away from each other to form high affinity metal ion sites in both the bidentate and potential tridentate settings. This indicates that the residues involved in the main ligand-binding pocket will have to move closer to each other during receptor activation. On the basis of the distance constraints from these activating metal ion sites, we propose a global toggle switch mechanism for 7TM receptor activation in which inward movement of the extracellular segments of especially TM-VI and, to some extent, TM-VII is coupled to the well established outward movement of the intracellular segments of these helices. We suggest that the pivots for these vertical seesaw movements are the highly conserved proline bends of the involved helices.
U2 - 10.1074/jbc.M512510200
DO - 10.1074/jbc.M512510200
M3 - Journal article
C2 - 16567806
SN - 0021-9258
VL - 281
SP - 17337
EP - 17346
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 25
ER -