TROSY- and CRINEPT-based NMR methods can select dramatically slower transverse relaxation NMR signals enabling studies of structures with sizes of 100 kDa and above.
- NMRFAM has tested and implemented new Agilent and Bruker pulse sequences for large macromolecules, including many designed for ILV(A) labeled proteins.
- Modern TROSY based pulse sequences (NH and CH ARTSY for protonated and perdeuterated proteins and for RNA/DNA aromatic CH and imino NH) to measure Residual Dipolar Couplings (RDCs) with high precision are implemented on NMRFAM’s Bruker and Agilent spectrometers.
Small angle X-ray scattering (SAXS) data can be collected and analyzed at NMRFAM. SAXS provides valuable low-resolution shape information that can be used in joint NMR-SAXS structure determination of large biomolecules.- NMRFAM can assist user with wheat germ cell-free protein synthesis for preparation of selectively-labeled proteins (including SAIL).