2dco

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 4: Line 4:
==Overview==
==Overview==
-
G protein-coupled receptors (GPCRs) control fundamental aspects of human, physiology and behaviors. Knowledge of their structures, especially for, the loop regions, is limited and has principally been obtained from, homology models, mutagenesis data, low resolution structural studies, and, high resolution studies of peptide models of receptor segments. We, developed an alternate methodology for structurally characterizing GPCR, loops, using the human S1P(4) first extracellular loop (E1) as a model, system. This methodology uses computational peptide designs based on, transmembrane domain (TM) model structures in combination with CD and NMR, spectroscopy. The characterized peptides contain segments that mimic the, self-assembling extracellular ends of TM 2 and TM 3 separated by E1, including residues R3.28(121) and E3.29(122) that are required for, sphingosine 1-phosphate (S1P) binding and receptor activation in the, S1P(4) receptor. The S1P(4) loop mimetic peptide interacted specifically, with an S1P headgroup analog, O-phosphoethanolamine (PEA), as evidenced by, PEA-induced perturbation of disulfide cross-linked coiled-coil first, extracellular loop mimetic (CCE1a) (1)H and (15)N backbone amide chemical, shifts. CCE1a was capable of weakly binding PEA near biologically relevant, residues R29 and E30, which correspond to R3.28 and E3.29 in the, full-length S1P(4) receptor, confirming that it has adopted a biologically, relevant conformation. We propose that the combination of coiled-coil TM, replacement and conformational stabilization with an interhelical, disulfide bond is a general design strategy that promotes native-like, structure for loops derived from GPCRs. (c) 2007 Wiley Periodicals, Inc., Biopolymers 86: 298-310, 2007.This article was originally published online, as an accepted preprint. The "Published Online" date corresponds to the, preprint version. You can request a copy of the preprint by emailing the, Biopolymers editorial office at biopolymers@wiley.com.
+
G protein-coupled receptors (GPCRs) control fundamental aspects of human physiology and behaviors. Knowledge of their structures, especially for the loop regions, is limited and has principally been obtained from homology models, mutagenesis data, low resolution structural studies, and high resolution studies of peptide models of receptor segments. We developed an alternate methodology for structurally characterizing GPCR loops, using the human S1P(4) first extracellular loop (E1) as a model system. This methodology uses computational peptide designs based on transmembrane domain (TM) model structures in combination with CD and NMR spectroscopy. The characterized peptides contain segments that mimic the self-assembling extracellular ends of TM 2 and TM 3 separated by E1, including residues R3.28(121) and E3.29(122) that are required for sphingosine 1-phosphate (S1P) binding and receptor activation in the S1P(4) receptor. The S1P(4) loop mimetic peptide interacted specifically with an S1P headgroup analog, O-phosphoethanolamine (PEA), as evidenced by PEA-induced perturbation of disulfide cross-linked coiled-coil first extracellular loop mimetic (CCE1a) (1)H and (15)N backbone amide chemical shifts. CCE1a was capable of weakly binding PEA near biologically relevant residues R29 and E30, which correspond to R3.28 and E3.29 in the full-length S1P(4) receptor, confirming that it has adopted a biologically relevant conformation. We propose that the combination of coiled-coil TM replacement and conformational stabilization with an interhelical disulfide bond is a general design strategy that promotes native-like structure for loops derived from GPCRs.
==About this Structure==
==About this Structure==
Line 13: Line 13:
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
-
[[Category: Kriwacki, R.W.]]
+
[[Category: Kriwacki, R W.]]
-
[[Category: Parrill, A.L.]]
+
[[Category: Parrill, A L.]]
-
[[Category: Pham, T.C.T.]]
+
[[Category: Pham, T C.T.]]
[[Category: 3-10 helix]]
[[Category: 3-10 helix]]
[[Category: coiled coil]]
[[Category: coiled coil]]
Line 21: Line 21:
[[Category: helix-turn-helix]]
[[Category: helix-turn-helix]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:46:27 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:57:27 2008''

Revision as of 14:57, 21 February 2008


2dco

Drag the structure with the mouse to rotate

S1P4 First Extracellular Loop Peptidomimetic

Overview

G protein-coupled receptors (GPCRs) control fundamental aspects of human physiology and behaviors. Knowledge of their structures, especially for the loop regions, is limited and has principally been obtained from homology models, mutagenesis data, low resolution structural studies, and high resolution studies of peptide models of receptor segments. We developed an alternate methodology for structurally characterizing GPCR loops, using the human S1P(4) first extracellular loop (E1) as a model system. This methodology uses computational peptide designs based on transmembrane domain (TM) model structures in combination with CD and NMR spectroscopy. The characterized peptides contain segments that mimic the self-assembling extracellular ends of TM 2 and TM 3 separated by E1, including residues R3.28(121) and E3.29(122) that are required for sphingosine 1-phosphate (S1P) binding and receptor activation in the S1P(4) receptor. The S1P(4) loop mimetic peptide interacted specifically with an S1P headgroup analog, O-phosphoethanolamine (PEA), as evidenced by PEA-induced perturbation of disulfide cross-linked coiled-coil first extracellular loop mimetic (CCE1a) (1)H and (15)N backbone amide chemical shifts. CCE1a was capable of weakly binding PEA near biologically relevant residues R29 and E30, which correspond to R3.28 and E3.29 in the full-length S1P(4) receptor, confirming that it has adopted a biologically relevant conformation. We propose that the combination of coiled-coil TM replacement and conformational stabilization with an interhelical disulfide bond is a general design strategy that promotes native-like structure for loops derived from GPCRs.

About this Structure

2DCO is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Peptide design and structural characterization of a GPCR loop mimetic., Pham TC, Kriwacki RW, Parrill AL, Biopolymers. 2007 Jul;86(4):298-310. PMID:17443712

Page seeded by OCA on Thu Feb 21 16:57:27 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools