1tz5: Difference between revisions
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New page: left|200px<br /> <applet load="1tz5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1tz5" /> '''[pNPY19-23]-hPP bound to DPC Micelles'''<br... |
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[[Image:1tz5.gif|left|200px]]<br /> | [[Image:1tz5.gif|left|200px]]<br /><applet load="1tz5" size="350" color="white" frame="true" align="right" spinBox="true" | ||
<applet load="1tz5" size=" | |||
caption="1tz5" /> | caption="1tz5" /> | ||
'''[pNPY19-23]-hPP bound to DPC Micelles'''<br /> | '''[pNPY19-23]-hPP bound to DPC Micelles'''<br /> | ||
==Overview== | ==Overview== | ||
Neuropeptide Y (NPY) and the pancreatic polypeptide (PP) are members of | Neuropeptide Y (NPY) and the pancreatic polypeptide (PP) are members of the neuropeptide Y family of hormones. They bind to the Y receptors with very different affinities: Whereas PP is highly selective for the Y(4) receptor, NPY displays highest affinites for Y(1), Y(2), and Y(5) receptor subtypes. Introducing the NPY segment 19-23 into PP leads to an increase in affinity at the Y(1) and Y(2) receptor subtypes whereas the exchange of this segment from PP into NPY leads to a large decrease in affinity at all receptor subtypes. PP displays a very stable structure in solution, with the N terminus being back-folded onto the C-terminal alpha-helix (the so-called PP-fold). The helix of NPY is less stable and the N terminus is freely diffusing in solution. The exchange of this segment, however, does not alter the PP-fold propensities of the chimeric peptides in solution. The structures of the phospholipid micelle-bound peptides serving to mimic the membrane-bound species display segregation into a more flexible N-terminal region and a well-defined alpha-helical region. The introduction of the [19-23]-pNPY segment into hPP leads to an N-terminal extension of the alpha-helix, now starting at Pro(14) instead of Met(17). In contrast, a truncated helix is observed in [(19)(-)(23)hPP]-pNPY, starting at Leu(17) instead of Ala(14). All peptides display moderate binding affinities to neutral membranes (K(assoc) in the range of 1.7 to 6.8 x 10(4) mol(-)(1) as determined by surface plasmon resonance) with the differences in binding being most probably related to the exchange of Arg-19 (pNPY) by Glu-23 (hPP). Differences in receptor binding properties between the chimeras and their parental peptides are therefore most likely due to changes in the conformation of the micelle-bound peptides. | ||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1TZ5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens_and_sus_scrofa Homo sapiens and sus scrofa] with NH2 as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http:// | 1TZ5 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens_and_sus_scrofa Homo sapiens and sus scrofa] 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=1TZ5 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Homo sapiens and sus scrofa]] | [[Category: Homo sapiens and sus scrofa]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Aguilar, M | [[Category: Aguilar, M I.]] | ||
[[Category: Beck-Sickinger, A | [[Category: Beck-Sickinger, A G.]] | ||
[[Category: Folkers, G.]] | [[Category: Folkers, G.]] | ||
[[Category: Kamimori, H.]] | [[Category: Kamimori, H.]] | ||
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[[Category: npy-pp chimera]] | [[Category: npy-pp chimera]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:18:52 2008'' | ||