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New page: left|200px<br /><applet load="1a13" size="450" color="white" frame="true" align="right" spinBox="true" caption="1a13" /> '''G PROTEIN-BOUND CONFORMATION OF MASTOPARAN-X...
 
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[[Image:1a13.gif|left|200px]]<br /><applet load="1a13" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1a13.gif|left|200px]]<br /><applet load="1a13" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1a13" />
caption="1a13" />
'''G PROTEIN-BOUND CONFORMATION OF MASTOPARAN-X, NMR, 14 STRUCTURES'''<br />
'''G PROTEIN-BOUND CONFORMATION OF MASTOPARAN-X, NMR, 14 STRUCTURES'''<br />


==Overview==
==Overview==
Mastoparans, a family of tetradecapeptides from wasp venom, have been used, as convenient low molecular weight models of receptors coupled to, GTP-binding regulatory proteins (G proteins) for the understanding of the, interaction between G proteins and receptors. Sukumar and Higashijima have, analyzed the conformation of mastoparan-X (MP-X) bound to the G protein, alpha-subunit using proton two-dimensional transferred nuclear Overhauser, effect (TRNOE) spectroscopy [Sukumar, M., and Higashijima, T. (1992) J., Biol. Chem., 267, 21421-21424]. The resultant structure, however, was not, well-defined due to severe overlap of peptide proton resonances. To, determine the G protein-bound conformation of MP-X in detail, we have, analyzed this interaction by heteronuclear multidimensional TRNOE, experiments of MP-X uniformly enriched with 15N and/or 13C. By solving the, overlap problem, we were able to determine the precise conformation of, MP-X bound to Gi1alpha: the peptide adopts an amphiphilic alpha-helix from, Trp3 to C-terminal Leu14, and the atomic root-mean-square deviation (rmsd), values in this portion about the averaged coordinates were 0.27 +/- 0.07 A, for the backbone atoms (N, Calpha, C') and 0.84 +/- 0.16 A for all heavy, atoms. These values are much smaller than the corresponding rmsd values of, the structures obtained from the proton 2D TRNOE spectrum alone: 1.70 +/-, 0.41 A for the backbone atoms (N, Calpha, C') and 2.84 +/- 0.51 A for all, heavy atoms. Our results indicate that the heteronuclear multidimensional, TRNOE experiments of peptides uniformly enriched with stable isotopes are, a very powerful tool for analyzing the conformation of short peptides, bound to large proteins. We will also discuss the structure-activity, relationships of mastoparans in activating G proteins on the basis of the, precise structure of MP-X bound to Gi1alpha.
Mastoparans, a family of tetradecapeptides from wasp venom, have been used as convenient low molecular weight models of receptors coupled to GTP-binding regulatory proteins (G proteins) for the understanding of the interaction between G proteins and receptors. Sukumar and Higashijima have analyzed the conformation of mastoparan-X (MP-X) bound to the G protein alpha-subunit using proton two-dimensional transferred nuclear Overhauser effect (TRNOE) spectroscopy [Sukumar, M., and Higashijima, T. (1992) J. Biol. Chem., 267, 21421-21424]. The resultant structure, however, was not well-defined due to severe overlap of peptide proton resonances. To determine the G protein-bound conformation of MP-X in detail, we have analyzed this interaction by heteronuclear multidimensional TRNOE experiments of MP-X uniformly enriched with 15N and/or 13C. By solving the overlap problem, we were able to determine the precise conformation of MP-X bound to Gi1alpha: the peptide adopts an amphiphilic alpha-helix from Trp3 to C-terminal Leu14, and the atomic root-mean-square deviation (rmsd) values in this portion about the averaged coordinates were 0.27 +/- 0.07 A for the backbone atoms (N, Calpha, C') and 0.84 +/- 0.16 A for all heavy atoms. These values are much smaller than the corresponding rmsd values of the structures obtained from the proton 2D TRNOE spectrum alone: 1.70 +/- 0.41 A for the backbone atoms (N, Calpha, C') and 2.84 +/- 0.51 A for all heavy atoms. Our results indicate that the heteronuclear multidimensional TRNOE experiments of peptides uniformly enriched with stable isotopes are a very powerful tool for analyzing the conformation of short peptides bound to large proteins. We will also discuss the structure-activity relationships of mastoparans in activating G proteins on the basis of the precise structure of MP-X bound to Gi1alpha.


==About this Structure==
==About this Structure==
1A13 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Vespa_simillima_xanthoptera Vespa simillima xanthoptera] with NH2 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1A13 OCA].  
1A13 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Vespa_simillima_xanthoptera Vespa simillima xanthoptera] with <scene name='pdbligand=NH2:'>NH2</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A13 OCA].  


==Reference==
==Reference==
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[[Category: mast cell degranulation]]
[[Category: mast cell degranulation]]


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