1z7x

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[[Image:1z7x.gif|left|200px]]
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{{STRUCTURE_1z7x| PDB=1z7x | SCENE= }}
{{STRUCTURE_1z7x| PDB=1z7x | SCENE= }}
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'''X-ray structure of human ribonuclease inhibitor complexed with ribonuclease I'''
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===X-ray structure of human ribonuclease inhibitor complexed with ribonuclease I===
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==Overview==
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The ribonuclease inhibitor protein (RI) binds to members of the bovine pancreatic ribonuclease (RNase A) superfamily with an affinity in the femtomolar range. Here, we report on structural and energetic aspects of the interaction between human RI (hRI) and human pancreatic ribonuclease (RNase 1). The structure of the crystalline hRI x RNase 1 complex was determined at a resolution of 1.95 A, revealing the formation of 19 intermolecular hydrogen bonds involving 13 residues of RNase 1. In contrast, only nine such hydrogen bonds are apparent in the structure of the complex between porcine RI and RNase A. hRI, which is anionic, also appears to use its horseshoe-shaped structure to engender long-range Coulombic interactions with RNase 1, which is cationic. In accordance with the structural data, the hRI.RNase 1 complex was found to be extremely stable (t(1/2)=81 days; K(d)=2.9 x 10(-16) M). Site-directed mutagenesis experiments enabled the identification of two cationic residues in RNase 1, Arg39 and Arg91, that are especially important for both the formation and stability of the complex, and are thus termed "electrostatic targeting residues". Disturbing the electrostatic attraction between hRI and RNase 1 yielded a variant of RNase 1 that maintained ribonucleolytic activity and conformational stability but had a 2.8 x 10(3)-fold lower association rate for complex formation and 5.9 x 10(9)-fold lower affinity for hRI. This variant of RNase 1, which exhibits the largest decrease in RI affinity of any engineered ribonuclease, is also toxic to human erythroleukemia cells. Together, these results provide new insight into an unusual and important protein-protein interaction, and could expedite the development of human ribonucleases as chemotherapeutic agents.
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(as it appears on PubMed at http://www.pubmed.gov), where 17350650 is the PubMed ID number.
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{{ABSTRACT_PUBMED_17350650}}
==About this Structure==
==About this Structure==
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[[Category: Ribonuclease-inhibitor complex]]
[[Category: Ribonuclease-inhibitor complex]]
[[Category: Structural genomic]]
[[Category: Structural genomic]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 17:17:20 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 03:45:31 2008''

Revision as of 00:45, 28 July 2008

Image:1z7x.png

Template:STRUCTURE 1z7x

X-ray structure of human ribonuclease inhibitor complexed with ribonuclease I

Template:ABSTRACT PUBMED 17350650

About this Structure

1Z7X is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Inhibition of human pancreatic ribonuclease by the human ribonuclease inhibitor protein., Johnson RJ, McCoy JG, Bingman CA, Phillips GN Jr, Raines RT, J Mol Biol. 2007 Apr 27;368(2):434-49. Epub 2007 Feb 9. PMID:17350650

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