Abstract

Nuclear magnetization storage, once limited by longitudinal and transverse relaxation lifetimes, T1 and T2, can be prolonged by symmetry-adapted nuclear spin order, i.e. long-lived states (LLS) and long-lived coherences (LLC), which have significantly extended relaxation time constants compared to T1 and T2, respectively. Excitation and/or detection of LLS currently involves pulses covering wide frequency ranges in high-magnetic-field spectrometers. This leads to excitation of unwanted signals that may overlap and interfere with the resonances of interest. Herein, we present a new pulse sequence that converts longitudinal magnetization to LLS and further to detectable magnetization using only frequency-selective pulses. We demonstrate the suitability of this sequence for different J-coupled spin pairs in dipeptide AlaGly and protein Ubiquitin. The newly developed method is adapted for investigations of LLS in complex systems such as proteins and mixtures of metabolites where selected molecular groups are to be investigated separately.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call