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          Institute: MPI für bioanorganische Chemie     Collection: MPI für bioanorganische Chemie     Display Documents



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ID: 683886.0, MPI für bioanorganische Chemie / MPI für bioanorganische Chemie
Expression, Purification, and Solid-State NMR Characterization of the Membrane Binding Heme Protein Nitrophorin 7 in Two Electronic Spin States
Authors:Varghese, Sabu; Yang, Fei; Pacheco, Victor; Wrede, Kathrin; Medvedev, Alexander; Ogata, Hideaki; Knipp, Markus; Heise, Henrike
Language:English
Date of Publication (YYYY-MM-DD):2013
Title of Journal:Biochemistry
Journal Abbrev.:Biochemistry
Volume:52
Start Page:7031
End Page:7040
Review Status:Peer-review
Audience:Experts Only
Abstract / Description:The nitrophorins (NPs) comprise a group of, NO transporting ferriheme b proteins found in the saliva of the blood sucking insect Rhodnius prolixus. In contrast to other nitrophorins (NP1-4), the recently identified membrane binding isoform NP7 tends to form oligomers and precipitates at higher concentrations in solution. Hence, solid-state NMR (ssNMR) was employed as an alternative method to gain structural insights on the precipitated protein. We report the expression and purification of C-13,N-15 isotopically labeled protein together with the first ssNMR characterization of NP7. Because the size of NP7 (21 kDa) still provides a challenge for ssNMR, the samples were reverse labeled with Lys and Val to reduce the number of crosspeaks in two-dimensional spectra. The two electronic spin states with S = 1/2 and S = 0 at the ferriheme iron were generated by the complexation with imidazole and NO, respectively. ssNMR spectra of both forms are well resolved, which allows for sequential resonance assignments of 22 residues. Importantly, the ssNMR spectra demonstrate that aggregation does not affect the protein fold. Comparison of the spectra of the two electronic spin states allows the determination of paramagnetically shifted cross peaks due to pseudocontact shifts, which assists the assignment of residues close to the heme center.
External Publication Status:published
Document Type:Article
Communicated by:N. N.
Affiliations:MPI für bioanorganische Chemie
External Affiliations:Varghese, S.; Pacheco, V.; Heise,. Forschungszentrum Jülich, ICS Inst Complex Syst Struct Biochem 6, D-2425 Julich, Germany.
Yang, F.; Miami Univ, Dept Chem & Biochem, Oxford, OH 45056 USA.
Identifiers:ISI:000326355500011 [ID No:1]
ISSN:0006-2960 [ID No:2]
DOI:10.1021/bi401020t [ID No:3]
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