001     7145
005     20200402205724.0
024 7 _ |2 pmid
|a pmid:19663495
024 7 _ |2 DOI
|a 10.1021/ja904897p
024 7 _ |2 WOS
|a WOS:000269379600020
037 _ _ |a PreJuSER-7145
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Chemistry, Multidisciplinary
100 1 _ |a Glück, J.M.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB89237
245 _ _ |a Integral membrane proteins in nanodiscs can be studied by solution NMR spectroscopy
260 _ _ |a Washington, DC
|b American Chemical Society
|c 2009
300 _ _ |a 12060 - 12061
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Journal of the American Chemical Society
|x 0002-7863
|0 8502
|y 34
|v 131
500 _ _ |a We thank Matthias Stoldt and Rudolf Hartmann for expert assistance and discussions. This work was supported by a grant from the Helmholtz Society ("Virtual Institute for Structural Biology") to D.W.
520 _ _ |a We present a two-dimensional solution NMR spectrum of an integral membrane protein (IMP) in a nanodisc. Solution NMR relies on rapid isotropic tumbling of the analyte with correlation times in the nanosecond range. IMPs in a cellular membrane do not satisfy this condition. Previous liquid-state NMR studies on IMPs were conducted in organic solvent or artificial membrane mimicking particles like detergent micelles. Nanodiscs are relatively small (150 kDa), detergent-free model membranes that are suitable for functional reconstitution of IMPs. Nanodiscs allow solubilization of integral membrane proteins in a nearly native lipid bilayer environment. The 70 residue polypeptide CD4mut was incorporated into nanodiscs. CD4mut features one transmembrane helix. The aliphatic (1)H-(13)C HSQC spectrum of nanodiscs with inserted, ((13)C, (15)N)-labeled CD4mut exhibits reasonably dispersed protein and lipid NMR signals. Our results demonstrate that IMPs in nanodiscs are amenable to liquid-state NMR methodology.
536 _ _ |a Funktion und Dysfunktion des Nervensystems
|c P33
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK409
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Antigens, CD4: chemistry
650 _ 2 |2 MeSH
|a Antigens, CD4: genetics
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Magnetic Resonance Spectroscopy
650 _ 2 |2 MeSH
|a Membrane Proteins: chemistry
650 _ 2 |2 MeSH
|a Membrane Proteins: genetics
650 _ 2 |2 MeSH
|a Membranes, Artificial
650 _ 2 |2 MeSH
|a Nanostructures: chemistry
650 _ 2 |2 MeSH
|a Solutions
650 _ 7 |0 0
|2 NLM Chemicals
|a Antigens, CD4
650 _ 7 |0 0
|2 NLM Chemicals
|a Membrane Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Membranes, Artificial
650 _ 7 |0 0
|2 NLM Chemicals
|a Solutions
650 _ 7 |a J
|2 WoSType
700 1 _ |a Wittlich, M.
|b 1
|u FZJ
|0 P:(DE-Juel1)VDB28257
700 1 _ |a Feuerstein, S.E.
|b 2
|u FZJ
|0 P:(DE-Juel1)VDB89238
700 1 _ |a Hoffmann, S.
|b 3
|u FZJ
|0 P:(DE-Juel1)VDB630
700 1 _ |a Willbold, D.
|b 4
|u FZJ
|0 P:(DE-Juel1)132029
700 1 _ |a Koenig, B. W.
|b 5
|u FZJ
|0 P:(DE-Juel1)132009
773 _ _ |a 10.1021/ja904897p
|g Vol. 131, p. 12060 - 12061
|p 12060 - 12061
|q 131<12060 - 12061
|0 PERI:(DE-600)1472210-0
|t Journal of the American Chemical Society
|v 131
|y 2009
|x 0002-7863
856 7 _ |u http://dx.doi.org/10.1021/ja904897p
909 C O |o oai:juser.fz-juelich.de:7145
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|l Funktion und Dysfunktion des Nervensystems
|b Gesundheit
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914 1 _ |y 2009
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |d 31.12.2010
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920 1 _ |0 I:(DE-82)080012_20140620
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981 _ _ |a I:(DE-Juel1)ICS-6-20110106
981 _ _ |a I:(DE-Juel1)VDB1346


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