Published April 1998 | Version v1
Journal article

HMQC and HSQC experiments with water flip-back optimized for large proteins

  • 1. Karolinska Institute, Department of Medical Biochemistry and Biophysics (Sweden)
  • 2. Zentrale Forschungseinheit, F. Hoffmann-La Roche AG (Switzerland)

Description

An HMQC experiment is proposed, dubbed FHMQC, where water flip-back is achieved by a single water-selective pulse preceding the basic HMQC pulse sequence. The scheme is demonstrated with a 15N, 1H-HMQC spectrum of uniformly 15N/2H-labelled S. aureus DNA gyrase B with a molecular weight of 45 kDa for the unlabelled protein. The sensitivity of the experiment is improved compared to that of an FHSQC spectrum. It is further shown that the original FHSQC experiment can be shortened by the use of bipolar gradients. Relaxation times of different 15N magnetizations and coherences were measured. The new FHMQC scheme is implemented in 3D NOESY-15N-HMQC and 3D15 N-HMQC-NOESY-15N-HMQC pulse sequences which are demonstrated with a 24 kDa fragment of uniformly 15N/13C/2H-labelled S. aureus DNA gyrase B

Additional details

Identifiers

Publishing Information

Journal Title
Journal of Biomolecular NMR
Journal Volume
11
Journal Issue
3
Journal Page Range
p. 279-288
ISSN
0925-2738

INIS

Country of Publication
Netherlands
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
39105487
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
CARBON 13; DEUTERIUM; DNA; HYDROGEN 1; MAGNETIZATION; MOLECULAR WEIGHT; NITROGEN 15; PROTEINS; RELAXATION; SENSITIVITY
Descriptors DEC
CARBON ISOTOPES; EVEN-ODD NUCLEI; HYDROGEN ISOTOPES; ISOTOPES; LIGHT NUCLEI; NITROGEN ISOTOPES; NUCLEI; NUCLEIC ACIDS; ODD-EVEN NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; STABLE ISOTOPES

Optional Information

Copyright
Copyright (c) 1998 Kluwer Academic Publishers