Paramagnetic relaxation enhancement to improve sensitivity of fast NMR methods: application to intrinsically disordered proteins
Creators
- 1. Leibniz Institute of Molecular Pharmacology (FMP), Department of NMR-assisted Structural Biology, In-cell NMR Group (Germany)
Description
We report enhanced sensitivity NMR measurements of intrinsically disordered proteins in the presence of paramagnetic relaxation enhancement (PRE) agents such as Ni2+-chelated DO2A. In proton-detected 1H-15N SOFAST-HMQC and carbon-detected (H-flip)13CO-15N experiments, faster longitudinal relaxation enables the usage of even shorter interscan delays. This results in higher NMR signal intensities per units of experimental time, without adverse line broadening effects. At 40 mmol·L−1 of the PRE agent, we obtain a 1.7- to 1.9-fold larger signal to noise (S/N) for the respective 2D NMR experiments. High solvent accessibility of intrinsically disordered protein (IDP) residues renders this class of proteins particularly amenable to the outlined approach.
Additional details
Identifiers
Publishing Information
- Journal Title
- Journal of Biomolecular NMR
- Journal Volume
- 51
- Journal Issue
- 4
- Journal Page Range
- p. 487-495
- ISSN
- 0925-2738
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 43093847
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARBON; LINE BROADENING; NICKEL IONS; NITROGEN 15; NUCLEAR MAGNETIC RESONANCE; PARAMAGNETISM; PROTEINS; PROTONS; RELAXATION; RESIDUES; SENSITIVITY; SIGNALS; SOLVENTS
- Descriptors DEC
- BARYONS; CHARGED PARTICLES; ELEMENTARY PARTICLES; ELEMENTS; FERMIONS; HADRONS; IONS; ISOTOPES; LIGHT NUCLEI; MAGNETIC RESONANCE; MAGNETISM; NITROGEN ISOTOPES; NONMETALS; NUCLEI; NUCLEONS; ODD-EVEN NUCLEI; ORGANIC COMPOUNDS; RESONANCE; STABLE ISOTOPES
Optional Information
- Copyright
- Copyright (c) 2011 Springer Science+Business Media B.V.