<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee M</submitter><funding>NIGMS NIH HHS</funding><pagination>263-77</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4160392</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>59(4)</volume><pubmed_abstract>Solid-state NMR spectra of membrane proteins often show significant line broadening at cryogenic temperatures. Here we investigate the effects of several cryoprotectants to preserve the spectral resolution of lipid membranes and membrane peptides at temperatures down to ~200 K. Trehalose, glycerol, dimethylsulfoxide (DMSO), dimethylformamide (DMF), and polyethylene glycol (PEG), were chosen. These compounds are commonly used in protein crystallography and cryobiology. 13C and 1H magic-angle-spinning spectra of several types of lipid membranes show that DMSO provides the best resolution enhancement over unprotected membranes and also best retards ice formation at low temperature. DMF and PEG-400 show slightly weaker cryoprotection, while glycerol and trehalose neither prevent membrane line </pubmed_abstract><journal>Journal of biomolecular NMR</journal><pubmed_title>Cryoprotection of lipid membranes for high-resolution solid-state  NMR studies of membrane peptides and proteins at low  temperature.</pubmed_title><pmcid>PMC4160392</pmcid><funding_grant_id>GM066976</funding_grant_id><funding_grant_id>GM088204</funding_grant_id><funding_grant_id>R01 GM066976</funding_grant_id><funding_grant_id>R01 GM088204</funding_grant_id><pubmed_authors>Hong M</pubmed_authors><pubmed_authors>Lee M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cryoprotection of lipid membranes for high-resolution solid-state  NMR studies of membrane peptides and proteins at low  temperature.</name><description>Solid-state NMR spectra of membrane proteins often show significant line broadening at cryogenic temperatures. Here we investigate the effects of several cryoprotectants to preserve the spectral resolution of lipid membranes and membrane peptides at temperatures down to ~200 K. Trehalose, glycerol, dimethylsulfoxide (DMSO), dimethylformamide (DMF), and polyethylene glycol (PEG), were chosen. These compounds are commonly used in protein crystallography and cryobiology. 13C and 1H magic-angle-spinning spectra of several types of lipid membranes show that DMSO provides the best resolution enhancement over unprotected membranes and also best retards ice formation at low temperature. DMF and PEG-400 show slightly weaker cryoprotection, while glycerol and trehalose neither prevent membrane line </description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Aug</publication><modification>2025-06-26T03:05:11.04Z</modification><creation>2025-06-26T03:05:11.04Z</creation></dates><accession>S-EPMC4160392</accession><cross_references><pubmed>25015530</pubmed><doi>10.1007/s10858-014-9845-z</doi></cross_references></HashMap>