The high-resolution NMR structure of a single-chain chimeric protein mimicking a SH3-peptide complex |
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Authors: | Candel Adela M Conejero-Lara Francisco Martinez Jose C van Nuland Nico A J Bruix Marta |
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Affiliation: | Departamento de Química Física e Instituto de Biotecnología, Facultad de Ciencias, Universidad de Granada, Campus Fuentenueva s/n, 18071 Granada, Spain. |
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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. |
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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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