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The high-resolution NMR structure of a single-chain chimeric protein mimicking a SH3-peptide complex
Authors:Candel Adela M  Conejero-Lara Francisco  Martinez Jose C  van Nuland Nico A J  Bruix Marta
Affiliation:Departamento de Química Física e Instituto de Biotecnología, Facultad de Ciencias, Universidad de Granada, Campus Fuentenueva s/n, 18071 Granada, Spain.
Abstract:
Here we present the high-resolution NMR structure of a chimera (SPCp41) between alpha-spectrin SH3 domain and the decapeptide p41. The tertiary structure mimics perfectly the interactions typically found in SH3-peptide complexes and is remarkably similar to that of the complex between the separate Spc-SH3 domain and ligand p41. Relaxation data confirm the tight binding between the ligand and SH3 part of the chimera. This chimera will serve as a tool for a deeper understanding of the relationship between structure and thermodynamics of binding using a combination of NMR, stability and site-directed mutagenesis studies, which can lead to an effective strategy for ligand design.
Keywords:SH3, Src-homology domain 3   Spc-SH3, SH3 domain of chicken brain α-spectrin   R21A Spc-SH3, the R21A mutant of Spc-SH3   p41, APSYSPPPPP decapeptide   SPCp41, single-chain chimeric protein made by fusion between Spc-SH3 and p41   NMR, nuclear magnetic resonance   NOESY, nuclear Overhauser enhancement spectroscopy   TOCSY, total correlation spectroscopy   RMSD, root mean square deviation
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