Abstract
Here, we report the high yield expression and preliminary structural analysis via solution hetero-nuclear NMR spectroscopy of the recombinant Met-1 human Angiogenin. The analysis reveals a well folded as well as, a monomeric polypeptide. Τhe sequence-specific assignment of its 1H, 15N and 13C resonances at high percentage was obtained. Also, using TALOS+ its secondary structure elements were determined.
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Abbreviations
- NMR:
-
Nuclear magnetic resonance
- HSQC:
-
Heteronuclear single quantum coherence
- Ang:
-
Angiogenin
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Acknowledgments
“SEE-DRUG” Grant (EU FP7 REGPOT CT-2011-285950; www.seedrug.upatras.gr), is acknowledged for financial support of this work. DSMC & DDL would like to acknowledge the financial support by the Postgraduate Programmes ‘‘Biotechnology-Quality assessment in Nutrition and the Environment”, ‘‘Application of Molecular Biology-Molecular Genetics-Molecular Markers”, Department of Biochemistry and Biotechnology, University of Thessaly.
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Aikaterini C. Tsika and Dimitra S. M. Chatzileontiadou have contributed equally to this work.
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Tsika, A.C., Chatzileontiadou, D.S.M., Leonidas, D.D. et al. NMR study of Met-1 human Angiogenin: 1H, 13C, 15N backbone and side-chain resonance assignment. Biomol NMR Assign 10, 379–383 (2016). https://doi.org/10.1007/s12104-016-9704-9
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DOI: https://doi.org/10.1007/s12104-016-9704-9