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dc.contributor.authorBarnes, Alexander
dc.contributor.authorMak-Jurkauskas, Melody L.
dc.contributor.authorMatsuki, Yoh
dc.contributor.authorBajaj, Vikram S.
dc.contributor.authorvan der Wel, Patrick C.A.
dc.contributor.authorSirigiri, Jagadishwar R.
dc.contributor.authorTemkin, Richard J.
dc.contributor.authorLugtenburg, Johan
dc.contributor.authorHerzfeld, Judith
dc.contributor.authorDeRocher, Ronald C.
dc.contributor.authorBryant, Jeffrey A.
dc.contributor.authorGriffin, Robert Guy
dc.date.accessioned2013-11-08T17:44:18Z
dc.date.available2013-11-08T17:44:18Z
dc.date.issued2009-03
dc.date.submitted2009-02
dc.identifier.issn10907807
dc.identifier.issn1096-0856
dc.identifier.urihttp://hdl.handle.net/1721.1/82050
dc.description.abstractWe describe a cryogenic sample exchange system that dramatically improves the efficiency of magic angle spinning (MAS) dynamic nuclear polarization (DNP) experiments by reducing the time required to change samples and by improving long-term instrument stability. Changing samples in conventional cryogenic MAS DNP/NMR experiments involves warming the probe to room temperature, detaching all cryogenic, RF, and microwave connections, removing the probe from the magnet, replacing the sample, and reversing all the previous steps, with the entire cycle requiring a few hours. The sample exchange system described here—which relies on an eject pipe attached to the front of the MAS stator and a vacuum jacketed dewar with a bellowed hole—circumvents these procedures. To demonstrate the excellent sensitivity, resolution, and stability achieved with this quadruple resonance sample exchange probe, we have performed high precision distance measurements on the active site of the membrane protein bacteriorhodopsin. We also include a spectrum of the tripeptide N-f-MLF-OH at 100 K which shows 30 Hz linewidths.en_US
dc.description.sponsorshipNational Institute for Biomedical Imaging and Bioengineering (U.S.) (Grant EB-002804)en_US
dc.description.sponsorshipNational Institute for Biomedical Imaging and Bioengineering (U.S.) (Grant EB-001960)en_US
dc.description.sponsorshipNational Institute for Biomedical Imaging and Bioengineering (U.S.) (Grant EB-001035)en_US
dc.description.sponsorshipNational Institute for Biomedical Imaging and Bioengineering (U.S.) (Grant EB-002026)en_US
dc.description.sponsorshipNational Institute for Biomedical Imaging and Bioengineering (U.S.) (Grant EB-003151)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.jmr.2009.03.003en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleCryogenic sample exchange NMR probe for magic angle spinning dynamic nuclear polarizationen_US
dc.typeArticleen_US
dc.identifier.citationBarnes, Alexander B., Melody L. Mak-Jurkauskas, Yoh Matsuki, Vikram S. Bajaj, Patrick C.A. van der Wel, Ronald DeRocher, Jeffrey Bryant, et al. “Cryogenic sample exchange NMR probe for magic angle spinning dynamic nuclear polarization.” Journal of Magnetic Resonance 198, no. 2 (June 2009): 261-270.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Plasma Science and Fusion Centeren_US
dc.contributor.departmentFrancis Bitter Magnet Laboratory (Massachusetts Institute of Technology)en_US
dc.contributor.mitauthorBarnes, Alexanderen_US
dc.contributor.mitauthorMak-Jurkauskas, Melody L.en_US
dc.contributor.mitauthorMatsuki, Yohen_US
dc.contributor.mitauthorBajaj, Vikram S.en_US
dc.contributor.mitauthorvan der Wel, Patrick C.A.en_US
dc.contributor.mitauthorDeRocher, Ronald C.en_US
dc.contributor.mitauthorBryant, Jeffrey A.en_US
dc.contributor.mitauthorSirigiri, Jagadishwar R.en_US
dc.contributor.mitauthorTemkin, Richard J.en_US
dc.contributor.mitauthorGriffin, Robert Guyen_US
dc.relation.journalJournal of Magnetic Resonanceen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsBarnes, Alexander B.; Mak-Jurkauskas, Melody L.; Matsuki, Yoh; Bajaj, Vikram S.; van der Wel, Patrick C.A.; DeRocher, Ronald; Bryant, Jeffrey; Sirigiri, Jagadishwar R.; Temkin, Richard J.; Lugtenburg, Johan; Herzfeld, Judith; Griffin, Robert G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1589-832X
dc.identifier.orcidhttps://orcid.org/0000-0001-9813-0177
dspace.mitauthor.errortrue
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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