Journal
MAGNETIC RESONANCE IN MEDICINE
Volume 49, Issue 3, Pages 440-449Publisher
JOHN WILEY & SONS INC
DOI: 10.1002/mrm.10398
Keywords
mobile proteins and peptides; mobile lipids; proton exchange; amide; macromolecules; cancer cells; rat brain; nuclear Overhauser effect; NOE
Funding
- NCRR NIH HHS [RR11115] Funding Source: Medline
- NIBIB NIH HHS [P41 EB015909] Funding Source: Medline
- NINDS NIH HHS [NS31490] Funding Source: Medline
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The mechanism of magnetization transfer (MT) between water and components of the proton spectrum was studied ex vivo in a perfused cell system and in vivo in the rat brain (n = 5). Water was selectively labeled and spectral buildup consequential to transfer of longitudinal magnetization was followed as a function of time. At short mixing time (T-m), nitrogen-bound solvent-exchangeable protons were observed, predominantly assigned to amide groups of proteins and peptides. At longer Tm, intramolecular nuclear Overhauser enhancement (NOE) was observed in the aliphatic proton region, leading to a mobile-macromolecule-weighted spectrum that resembles typical protein spectra described in the literature. This effect on the proton spectrum is distinct from that of classical off-resonance MT, which has been shown to be due to the immobile solid-like proton pool. When studying a solution of major brain metabolites under physiological concentrations and conditions (pH), no transfer effects were observed, in line with expectations based on reduced NOE effects in rapidly tumbling molecules and the fast proton exchange rates of amino, amine, SH, and OH groups. The spectral intensities of the amide protons may serve as indicators for pH and cellular levels of mobile proteins and peptides, while the aliphatic components are representative of several types of mobile macromolecules, including proteins, peptides, and lipids. (C) 2003 Wiley-Liss, Inc.
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