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Numerous studies have investigated the differences and similarities between protein structures determined by solution NMR spectroscopy and those determined by X-ray crystallography. A fundamental question is whether any observed differences are due to differing methodologies or to differences in the behavior of proteins in solution versus in the crystalline state. Here, we compare the properties of the hydrophobic cores of high-resolution protein crystal structures and those in NMR structures, determined using increasing numbers and types of restraints. Prior studies have reported that many NMR structures have denser cores compared with those of high-resolution X-ray crystal structures. Our current work investigates this result in more detail and finds that these NMR structures tend to violate basic features of protein stereochemistry, such as small non-bonded atomic overlaps and few Ramachandran and sidechain dihedral angle outliers. We find that NMR structures solved with more restraints, and which do not significantly violate stereochemistry, have hydrophobic cores that have a similar size and packing fraction as their counterparts determined by X-ray crystallography at high resolution. These results lead us to conclude that, at least regarding the core packing properties, high-quality structures determined by NMR and X-ray crystallography are the same, and the differences reported earlier are most likely a consequence of methodology, rather than fundamental differences between the protein in the two different environments.
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http://dx.doi.org/10.1002/pro.4373 | DOI Listing |
Can J Cardiol
September 2025
Division of Cardiology, Hartford HealthCare Heart and Vascular Institute, Hartford, CT, USA. Electronic address:
Post-transplant rejection surveillance remains a cornerstone of heart transplant care. Although endomyocardial biopsy (EMB) has long been the gold standard for detecting rejection, its invasive nature, interobserver variability in histologic interpretation, and limitations in distinguishing between acute cellular rejection (ACR) and antibody-mediated rejection have prompted interest in noninvasive techniques. Traditional biomarkers- such as troponin, C-reactive protein, brain natriuretic peptide, and donor-specific antibodies- offer supplementary assessments of graft function but lack the specificity and sensitivity required to be standalone markers.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Materials Science and Engineering, Korea University, Seoul 02841, Republic of Korea.
The thermodynamic equilibrium assumption often invoked in modeling ion migration in solid-state materials remains insufficient to capture the true migration behavior of Li ions, particularly in less-crystalline superionic conductors that exhibit anomalously high Li ion conductivity. Such materials challenge classical frameworks and necessitate a lattice dynamics-based perspective that explicitly accounts for nonequilibrium phonon interactions and transient structural responses. Here, we uncover a phonon-governed Li ion migration mechanism in garnet-structured superionic conductors by comparing Ta-doped LiLaZrTaO (LLZTO4) to its undoped analogue, LiLaZrAlO (LLZO).
View Article and Find Full Text PDFNat Commun
September 2025
Clinical Memory Research Unit, Department of Clinical Sciences Malmö, Faculty of Medicine, Lund University, Lund, Sweden.
The distribution of tau pathology in Alzheimer's disease (AD) shows remarkable inter-individual heterogeneity, including hemispheric asymmetry. However, the factors driving this asymmetry remain poorly understood. Here we explore whether tau asymmetry is linked to i) reduced inter-hemispheric brain connectivity (potentially restricting tau spread), or ii) asymmetry in amyloid-beta (Aβ) distribution (indicating greater hemisphere-specific vulnerability to AD pathology).
View Article and Find Full Text PDFProg Nucl Magn Reson Spectrosc
July 2025
Institute of Molecular Physical Science, ETH Zurich, Zurich, Switzerland; Institute of Biophysical Chemistry, Goethe University Frankfurt, Frankfurt am Main, Germany; Department of Chemistry, Tokyo Metropolitan University, Hachioji, Tokyo, Japan. Electronic address:
NMR spectroscopy is a versatile technique for studies of molecular structures, dynamic processes, and intermolecular interactions across a broad range of systems, including small molecules, macromolecules, biomolecular assemblies, and materials in both solution and solid-state environments. As the complexity of NMR studies continues to pose challenges for practitioners, the integration of machine learning is recognized as a promising research direction for improving data acquisition, processing, and analysis. Here, we summarize recent findings in this area, highlighting common applications such as signal detection, chemical shift assignment, structure determination, chemical shift prediction, non-uniform sampling reconstruction, and denoising.
View Article and Find Full Text PDFProg Nucl Magn Reson Spectrosc
September 2025
Magnetic Resonance Center (CERM) and Department of Chemistry "Ugo Schiff", University of Florence, Via L. Sacconi 6, 50019 Sesto Fiorentino, Italy. Electronic address:
Studying multidomain proteins, especially those combining well-folded domains with intrinsically disordered regions (IDRs), requires specific Nuclear Magnetic Resonance (NMR) techniques to address their structural complexity. To illustrate this, we focus here on the nucleocapsid protein from SARS-CoV-2, which includes both structured and disordered regions. We applied a suite of NMR methods, combining ARTINA software for automatic assignment and structure modelling with multi-receiver experiments that simultaneously capture signals from different nuclear spins, increasing both data quality and acquisition efficiency.
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