This title appears in the Scientific Report : 2013 

Expression, Purification, and Solid-State NMR Characterization of the Membrane Binding Heme Protein Nitrophorin 7 in Two Electronic Spin States
Varghese, Sabu
Yang, Fei / Pacheco, Victor / Wrede, Kathrin / Medvedev, Alexander / Ogata, Hideaki / Knipp, Markus (Corresponding author) / Heise, Henrike
Strukturbiochemie ; ICS-6
Biochemistry, 52 (2013) 40, S. 7031 - 7040
Columbus, Ohio American Chemical Society 2013
10.1021/bi401020t
24033104
Journal Article
Structural Biology
Please use the identifier: http://dx.doi.org/10.1021/bi401020t in citations.
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 13C,15N 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.