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4,4'-dithiobisdipicolinic acid: a small and convenient lanthanide binding tag for protein NMR spectroscopy

dc.contributor.authorJia, Xinyingen_AU
dc.contributor.authorMaleckis, Ansisen_AU
dc.contributor.authorOtting, Gottfrieden_AU
dc.contributor.authorHuber, Thomasen_AU
dc.date.accessioned2015-12-10T22:51:11Z
dc.date.issued2011
dc.date.updated2016-02-24T10:24:15Z
dc.description.abstractPseudocontact shifts (PCS) from paramagnetic lanthanide ions present powerful long-range structure restraints for studies of proteins by nuclear magnetic resonance spectroscopy. To elicit PCSs, the lanthanide must be attached site-specifically to the target protein. In addition, it needs to be attached rigidly to avoid averaging of the PCSs due to mobility with respect to the protein and it must not interfere with the function of the protein. Here, we present a dipicolinic acid reagent that spontaneously forms a disulfide bond with thiol groups of accessible cysteine residues. A minimal number of rotatable bonds between the cysteine side chain and the tag helps to minimise mobility. Combined with the small size of the tag and quantitative tagging yields, these features make it a highly attractive tool for generating structure restraints by paramagnetic lanthanides.
dc.identifier.issn0947-6539
dc.identifier.urihttp://hdl.handle.net/1885/58929
dc.publisherWiley-VCH Verlag GMBH
dc.sourceChemistry, A European Journal
dc.subjectKeywords: Lanthanides; NMR spectroscopy; protein labeling; pseudocontact shifts; thiol-reactive reagent; Amino acids; Chemical reactions; Covalent bonds; Nuclear magnetic resonance; Paramagnetic materials; Paramagnetism; Proteins; Rare earth elements; Resonance; Nu lanthanides; NMR spectroscopy; protein labeling; pseudocontact shifts; thiol-reactive reagent
dc.title4,4'-dithiobisdipicolinic acid: a small and convenient lanthanide binding tag for protein NMR spectroscopy
dc.typeJournal article
local.bibliographicCitation.issue24
local.bibliographicCitation.lastpage6836
local.bibliographicCitation.startpage6830
local.contributor.affiliationJia, Xinying, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationMaleckis, Ansis, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHuber, Thomas, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationOtting, Gottfried, College of Physical and Mathematical Sciences, ANU
local.contributor.authoruidJia, Xinying, u4394742
local.contributor.authoruidMaleckis, Ansis, u4777328
local.contributor.authoruidHuber, Thomas, u9512183
local.contributor.authoruidOtting, Gottfried, u4046684
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor060112 - Structural Biology (incl. Macromolecular Modelling)
local.identifier.absfor030606 - Structural Chemistry and Spectroscopy
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.absseo860803 - Human Pharmaceutical Treatments (e.g. Antibiotics)
local.identifier.ariespublicationu4005981xPUB465
local.identifier.citationvolume17
local.identifier.doi10.1002/chem.201003573
local.identifier.scopusID2-s2.0-79957940344
local.identifier.thomsonID000292201000031
local.type.statusPublished Version

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