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• W2944780702 abstract "Although magnetization transfer (MT) has been widely used in brain MRI, for example in brain inflammation and multiple sclerosis, the detailed molecular origin of MT effects and the role that proteins play in MT remain unclear. In this work, a proteoliposome model system was used to mimic the myelin environment and to examine the roles of protein, cholesterol, brain cerebrosides, and sphingomyelin embedded in the liposome matrix. Exchange parameters were determined using a double-quantum filter experiment. The goal was to determine the relative contributions to exchange and MT of cerebrosides, sphingomyelin, cholesterol, and proteins in 1,2-dimyristoyl-sn-glycero-3-phosphocholine bilayers. The main finding was that cerebrosides produced the strongest exchange effects, and that these were even more pronounced than those found for proteins. Sphingomyelin (which also has exchangeable groups at the head of the fatty acid chains, albeit closer to the lipid acyl chains) and cholesterol showed only minimal transfer. Overall, the extracted exchange rates appeared much smaller than commonly assumed for -OH and -NH groups." @default.
• W2944780702 created "2019-05-16" @default.
• W2944780702 creator A5015330931 @default.
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• W2944780702 date "2019-05-06" @default.
• W2944780702 modified "2023-10-14" @default.
• W2944780702 title "Magnetization transfer in liposome and proteoliposome samples that mimic the protein and lipid composition of myelin" @default.
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• W2944780702 doi "https://doi.org/10.1002/nbm.4097" @default.
• W2944780702 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6581629" @default.
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