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PMID: 15755445 Published · ppublish English Journal Article

Intramolecular cooperativity in a protein binding site assessed by combinatorial shotgun scanning mutagenesis.

Journal of molecular biology ·Vol. 347 ·No. 3 ·2005-04-01 ·Pages 489-94

Pál G, Ultsch MH, Clark KP, Currell B, Kossiakoff AA, Sidhu SS

Abstract

Combinatorial shotgun alanine-scanning was used to assess intramolecular cooperativity in the high affinity site (site 1) of human growth hormone (hGH) for binding to its receptor. A total of 19 side-chains were analyzed and statistically significant data were obtained for 145 of the 171 side-chain pairs. The analysis revealed that 90% of the side-chain pairs exhibited no statistically significant pair interactions, and the remaining 10% of side-chain pairs exhibited only small interactions corresponding to cooperative interaction energies with magnitudes less than 0.4 kcal/mol. The statistical predictions were tested by measuring affinities for purified mutant proteins and were found to be accurate for five of six side-chain pairs tested. The results reveal that hGH site 1 behaves in a highly additive manner and suggest that shotgun scanning should be useful for assessing cooperative effects in other protein-protein interactions.

MeSH Terms
Binding Sites Human Growth Hormone/chemistry,genetics,metabolism Humans Membrane Proteins/chemistry,genetics,metabolism Models, Molecular Mutagenesis Protein Binding Protein Structure, Tertiary
Chemicals
Membrane Proteins delta-hGHR Human Growth Hormone
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Pál Gábor
Department of Biochemistry and Molecular Biology and Institute for Biophysical Dynamics, Cummings Life Sciences Center, University of Chicago, 920 East 58th Street, Chicago, IL 60637, USA.
Ultsch Mark H
Clark Kevin P
Currell Bridget
Kossiakoff Anthony A
Sidhu Sachdev S
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
2005-04-01
Pages
489-94
Language
English
Region
England
NLM ID
2985088R
Subset
IM
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