Measuring transverse relaxation in highly paramagnetic systems

• Published in: Journal of biomolecular NMR 2020-09, Vol.74 (8-9), p.431-442
• Main Authors: Invernici, Michele, Trindade, Inês B., Cantini, Francesca, Louro, Ricardo O., Piccioli, Mario
• Format: Article
• Language: English
• Subjects: Biochemistry; Biological and Medical Physics; Biophysics; Physics; Physics and Astronomy; Spectroscopy/Spectrometry
• ISSN: 0925-2738; 1573-5001
• DOI: 10.1007/s10858-020-00334-w

The enhancement of nuclear relaxation rates due to the interaction with a paramagnetic center (known as Paramagnetic Relaxation Enhancement) is a powerful source of structural and dynamics information, widely used in structural biology. However, many signals affected by the hyperfine interaction relax faster than the evolution periods of common NMR experiments and therefore they are broadened beyond detection. This gives rise to a so-called blind sphere around the paramagnetic center, which is a major limitation in the use of PREs. Reducing the blind sphere is extremely important in paramagnetic metalloproteins. The identification, characterization, and proper structural restraining of the first coordination sphere of the metal ion(s) and its immediate neighboring regions is key to understand their biological function. The novel HSQC scheme we propose here, that we termed R 2 -weighted, HSQC-AP, achieves this aim by detecting signals that escaped detection in a conventional HSQC experiment and provides fully reliable R 2 values in the range of 1 H R 2 rates ca. 50–400 s −1 . Independently on the type of paramagnetic center and on the size of the molecule, this experiment decreases the radius of the blind sphere and increases the number of detectable PREs. Here, we report the validation of this approach for the case of PioC, a small protein containing a high potential 4Fe-4S cluster in the reduced [Fe 4 S 4 ] 2+ form. The blind sphere was contracted to a minimal extent, enabling the measurement of R 2 rates for the cluster coordinating residues.