Paramagnetic-iterative relaxation matrix approach: extracting PRE-restraints from NOESY spectra for 3D structure elucidation of biomolecules

• Published in: Journal of biomolecular NMR Vol. 73; no. 12; pp. 699 - 712
• Main Authors: Cetiner, E. C., Jonker, H. R. A., Helmling, C., Gophane, D. B., Grünewald, C., Sigurdsson, S. Th, Schwalbe, H.
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.12.2019; Springer Nature B.V
• Subjects: Biochemistry; Biological and Medical Physics; Biomolecules; Biophysics; Chemical equilibrium; Constraints; Diamagnetism; Electron Spin Resonance Spectroscopy; Evaluation; Impact analysis; Labeling; Labels; Mathematical analysis; Molecular Conformation; NMR; Nuclear magnetic resonance; Nuclear Magnetic Resonance, Biomolecular - methods; Nucleic Acid Conformation; Organic chemistry; Physics; Physics and Astronomy; Quality assessment; Ribonucleic acid; RNA; RNA - chemistry; Spectroscopy/Spectrometry; Spin Labels; PRE; NMR; RNA; Spin label; NOESY; IRMA; Paramagnetic
• ISSN: 0925-2738; 1573-5001
• DOI: 10.1007/s10858-019-00282-0

Paramagnetic relaxation enhancement (PRE) can be used to determine long-range distance restraints in biomolecules. The PREs are typically determined by analysis of intensity differences in HSQC experiments of paramagnetic and diamagnetic spin labels. However, this approach requires both isotope- and spin-labelling. Herein, we report a novel method to evaluate NOESY intensities in the presence of a paramagnetic moiety to determine PRE restraints. The advantage of our approach over HSQC-based approaches is the increased number of available signals without the need for isotope labelling. NOESY intensities affected by a paramagnetic center were evaluated during a structure calculation within the paramagnetic iterative relaxation matrix approach (P-IRMA). We applied P-IRMA to a 14-mer RNA with a known NMR solution structure, which allowed us to assess the quality of the PRE restraints. To this end, three different spin labels have been attached at different positions of the 14-mer to test the influence of flexibility on the structure calculation. Structural disturbances introduced by the spin label have been evaluated by chemical shift analysis. Furthermore, the impact of P-IRMA on the quality of the structure bundles were tested by intentionally leaving out available diamagnetic restraints. Our analyses show that P-IRMA is a powerful tool to refine RNA structures for systems that are insufficiently described by using only diamagnetic restraints.