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1z5f

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(New page: 200px<br /><applet load="1z5f" size="450" color="white" frame="true" align="right" spinBox="true" caption="1z5f" /> '''Solution Structure of the Cytotoxic RC-RNase...)
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'''Solution Structure of the Cytotoxic RC-RNase 3 with a Pyroglutamate Residue at the N-terminus'''<br />
'''Solution Structure of the Cytotoxic RC-RNase 3 with a Pyroglutamate Residue at the N-terminus'''<br />
==Overview==
==Overview==
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Many proteins and bioactive peptides contain an N-terminal pyroglutamate, residue (Pyr1). This residue reduces the susceptibility of the protein to, aminopeptidases and often has important functional roles. The antitumor, ribonuclease RC-RNase 3 (RNase 3) from oocytes of Rana catesbeiana, (bullfrog) is one such protein. We have produced recombinant RNase 3, containing the N-terminal Pyr1 (pRNase 3) and found it to be, indistinguishable from the native RNase 3 by mass spectrometry and a, variety of other biochemical and immunological criteria. We demonstrated, by NMR analysis that the Pyr1 of pRNase 3 forms hydrogen bonds with Lys9, and Ile96 and stabilizes the N-terminal alpha-helix in a rigid, conformation. In contrast, the N-terminal alpha-helix becomes flexible and, the pKa values of the catalytic residues His10 and His97 altered when Pyr1, formation is blocked by an extra methionine at the N terminus in the, recombinant mqRNase 3. Thus, our results provide a mechanistic explanation, on the essential role of Pyr1 in maintaining the structural integrity, especially at the N-terminal alpha-helix, and in providing the proper, environment for the ionization of His10 and His97 residues for catalysis, and cytotoxicity against HeLa cells.
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Many proteins and bioactive peptides contain an N-terminal pyroglutamate residue (Pyr1). This residue reduces the susceptibility of the protein to aminopeptidases and often has important functional roles. The antitumor ribonuclease RC-RNase 3 (RNase 3) from oocytes of Rana catesbeiana (bullfrog) is one such protein. We have produced recombinant RNase 3 containing the N-terminal Pyr1 (pRNase 3) and found it to be indistinguishable from the native RNase 3 by mass spectrometry and a variety of other biochemical and immunological criteria. We demonstrated by NMR analysis that the Pyr1 of pRNase 3 forms hydrogen bonds with Lys9 and Ile96 and stabilizes the N-terminal alpha-helix in a rigid conformation. In contrast, the N-terminal alpha-helix becomes flexible and the pKa values of the catalytic residues His10 and His97 altered when Pyr1 formation is blocked by an extra methionine at the N terminus in the recombinant mqRNase 3. Thus, our results provide a mechanistic explanation on the essential role of Pyr1 in maintaining the structural integrity, especially at the N-terminal alpha-helix, and in providing the proper environment for the ionization of His10 and His97 residues for catalysis and cytotoxicity against HeLa cells.
==About this Structure==
==About this Structure==
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1Z5F is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rana_catesbeiana Rana catesbeiana]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Z5F OCA].
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1Z5F is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Rana_catesbeiana Rana catesbeiana]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Z5F OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Chen, C.]]
[[Category: Chen, C.]]
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[[Category: Huang, Y.C.]]
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[[Category: Huang, Y C.]]
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[[Category: Liao, Y.D.]]
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[[Category: Liao, Y D.]]
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[[Category: Lou, Y.C.]]
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[[Category: Lou, Y C.]]
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[[Category: Pan, Y.R.]]
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[[Category: Pan, Y R.]]
[[Category: bullfrog]]
[[Category: bullfrog]]
[[Category: cytotoxicity]]
[[Category: cytotoxicity]]
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[[Category: ribonuclease]]
[[Category: ribonuclease]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 04:44:43 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:12:15 2008''

Revision as of 14:12, 21 February 2008


1z5f

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Solution Structure of the Cytotoxic RC-RNase 3 with a Pyroglutamate Residue at the N-terminus

Overview

Many proteins and bioactive peptides contain an N-terminal pyroglutamate residue (Pyr1). This residue reduces the susceptibility of the protein to aminopeptidases and often has important functional roles. The antitumor ribonuclease RC-RNase 3 (RNase 3) from oocytes of Rana catesbeiana (bullfrog) is one such protein. We have produced recombinant RNase 3 containing the N-terminal Pyr1 (pRNase 3) and found it to be indistinguishable from the native RNase 3 by mass spectrometry and a variety of other biochemical and immunological criteria. We demonstrated by NMR analysis that the Pyr1 of pRNase 3 forms hydrogen bonds with Lys9 and Ile96 and stabilizes the N-terminal alpha-helix in a rigid conformation. In contrast, the N-terminal alpha-helix becomes flexible and the pKa values of the catalytic residues His10 and His97 altered when Pyr1 formation is blocked by an extra methionine at the N terminus in the recombinant mqRNase 3. Thus, our results provide a mechanistic explanation on the essential role of Pyr1 in maintaining the structural integrity, especially at the N-terminal alpha-helix, and in providing the proper environment for the ionization of His10 and His97 residues for catalysis and cytotoxicity against HeLa cells.

About this Structure

1Z5F is a Single protein structure of sequence from Rana catesbeiana. Full crystallographic information is available from OCA.

Reference

Roles of N-terminal pyroglutamate in maintaining structural integrity and pKa values of catalytic histidine residues in bullfrog ribonuclease 3., Lou YC, Huang YC, Pan YR, Chen C, Liao YD, J Mol Biol. 2006 Jan 20;355(3):409-21. Epub 2005 Nov 10. PMID:16309702

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