Abstract
The assignment of aromatic side-chain spins has always been more challenging than assigning backbone and aliphatic spins. Selective labeling combined with mutagenesis has been the approach for assigning aromatic spins. This manuscript reports a method for assigning aromatic spins in a fully protonated protein by connecting them to the backbone atoms using a low-power TOBSY sequence. The pulse sequence employs residual polarization and sequential acquisitions techniques to record H(N)- and H(C)-detected spectra in a single experiment. The unambiguous assignment of aromatic spins also enables the characterization of (1)H-(1)H distance restraints involving aromatic spins. Broadband (RFDR) and selective (BASS-SD) recoupling sequences were used to generate H(N)-Η(C), H(C)-H(N) and H(C)-H(C) restraints involving the side-chain proton spins of aromatic residues. This approach has been demonstrated on a fully protonated U-[(13)C,(15)N] labeled GB1 sample at 95-100 kHz MAS.