Puntuación de arriba hacia abajo de la aptitud espectral mediante análisis de imágenes para la validación de la...

Nuclear magnetic resonance (NMR) spectroscopy is a powerful technique for protein structure determination, but traditional approaches require extensive manual assignments of hundreds to thousands of resonances. Here, we present NMRFAM-BPHON, a novel "top-down" approach that treats experimental NMR spectra as continuous grayscale images and quantitatively scores the agreement with simulated spectra generated from candidate protein structures. This method does not require complete resonance assignments, although it can incorporate experimental chemical shifts when available to improve performance. The simulated spectra are generated from postulated resonance assignments, which can be derived from empirical database predictions, direct interpretations, or a hybrid combination. BPHON employs a physics-based approximate polarization transfer model to predict cross-peak intensities from the internuclear distances in the decoy structure and models the peak line shapes using empirical, bulk T₂ relaxation rates and literature values for scalar couplings. The resulting simulated spectra are scored relative to the experimental data by normalized cross correlation, yielding fitness scores between 0 and 1. We demonstrate BPHON's ability to discriminate structural models, particularly in the case of ¹³C-detected magic angle spinning solid-state NMR spectra. The software is packaged with a user-friendly graphical user interface for ChimeraX, enabling advanced NMR analysis accessible without requiring extensive manual analysis.