An improved, time-efficient approach to extract accurate distance restraints for NMR<sup>2</sup>structure calculation
- Author(s)
- Aditya Pokharna, Felix Torres, Harindranath Kadavath, Julien Orts, Roland Riek
- Abstract
Exact nuclear Overhauser enhancement (eNOE) yields highly accurate, ensemble averaged 1H-1H distance restraints with an accuracy of up to 0.1 Å for the multi-state structure determination of proteins as well as for nuclear magnetic resonance molecular replacement (NMR2) to determine the structure of the protein-ligand interaction site in a time-efficient manner. However, in the latter application, the acquired eNOEs lack the obtainable precision of 0.1 Å because of the asymmetrical nature of the filtered nuclear Overhauser enhancement spectroscopy (NOESY) experiment used in NMR2. This error is further propagated to the eNOE equations used to fit and extract the distance restraints. In this work, a new analysis method is proposed to obtain inter-molecular distance restraints from the filtered NOESY spectrum more accurately and intuitively by dividing the NOE cross peak by the corresponding diagonal peak of the ligand. The method termed diagonal-normalised eNOEs was tested on the data acquired by on the complex of PIN1 and a small, weak-binding phenylimidazole fragment. NMR2 calculations performed using the distances derived from diagonal-normalised eNOEs yielded the right orientation of the fragment in the binding pocket and produced a structure that more closely resembles the benchmark X-ray structure (2XP6) with an average heavy-atom root-mean-square deviation (RMSD) of 1.681 Å with respect to it, when compared to the one produced with traditional NMR2 with an average heavy atom RMSD of 3.628 Å. This is attributed to the higher precision of the evaluated distance restraints.
- Organisation(s)
- Department of Pharmaceutical Sciences
- External organisation(s)
- Eidgenössische Technische Hochschule Zürich, Universität Wien
- Journal
- Magnetic Resonance
- Volume
- 3
- Pages
- 137-144
- No. of pages
- 8
- ISSN
- 2699-0016
- DOI
- https://doi.org/10.5194/mr-3-137-2022
- Publication date
- 08-2022
- Peer reviewed
- Yes
- Austrian Fields of Science 2012
- 106002 Biochemistry, 106006 Biophysics
- ASJC Scopus subject areas
- Analytical Chemistry, Condensed Matter Physics, Atomic and Molecular Physics, and Optics
- Portal url
- https://ucris.univie.ac.at/portal/en/publications/an-improved-timeefficient-approach-to-extract-accurate-distance-restraints-for-nmr2structure-calculation(acedd6c4-8b9d-404d-a1e5-d6b1036366e8).html