Laage, SegoleneLesage, AnneEmsley, LyndonBertini, IvanoFelli, Isabella C.Pierattelli, RobertaPintacuda, Guido2015-01-082015-01-082015-01-08200910.1021/ja903542hhttps://infoscience.epfl.ch/handle/20.500.14299/110034WOS:000268806500011A transverse-dephasing optimized (SE)-E-3 (spin-state selective excitation) method is implemented in solid-state NMR experiments of uniformly labeled protein samples, and it is shown to provide a simultaneous significant gain in both resolution (up to a factor of 2.2) and sensitivity (up to a factor of 1.4). This is illustrated with high-resolution NCO and NCA correlations of a microcrystalline sample of the oxidized form of the 153 residue human Cu(II)Zn(II) superoxide dismutase (SOD), a dimeric paramagnetic enzyme of 32 kDa. This method allows the resolution of 145 signals in the highly crowded carbonyl region in the NCO correlation spectrum.Transverse-Dephasing Optimized Homonuclear J-Decoupling in Solid-State NMR Spectroscopy of Uniformly C-13-Labeled Proteinstext::journal::journal article::research article