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Local molecular composition across cell membrane microenvironments exerts profound effects on cellular physiology and pathology. Yet spatial demarcation of identical biomolecules inside and outside lipid raft microdomains has not been determined. Here we report location-differentiated DNA hierarchical cyclic construction for lipid raft-differentiated spatial profiling of identical biomolecules in living cells. It contains two sequential DNA cyclic construction reactions: primary one triggered by total target molecules and secondary one activated by lipid raft's location markers proximal to target molecules. Using this method, we differentially visualize identical biomolecules localized in lipid raft and non-lipid raft microdomains with different signals. We demonstrate the robustness and universality of this method by testing cell surface RNAs and proteins in diverse cell types. We reveal their diverse spatial demarcation with intrinsic heterogeneity. In both lipid raft-disrupting cells and senescent cells, MUC1 protein is dynamically organized between these two microdomains. Our strategy provides a promising avenue to investigate physiological and pathological functions of dynamic molecular compositions across cellular microenvironments.
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http://dx.doi.org/10.1002/anie.202505249 | DOI Listing |
FEBS J
September 2025
Neutron Scattering Division, Oak Ridge National Laboratory, USA.
Serine hydroxymethyltransferase (SHMT) is a critical enzyme in the one-carbon (1C) metabolism pathway catalyzing the reversible conversion of L-Ser into Gly and concurrent transfer of 1C unit to tetrahydrofolate (THF) to give 5,10-methylene-THF (5,10-MTHF), which is used in the downstream syntheses of biomolecules critical for cell proliferation. The cellular 1C metabolism is hijacked by many cancer types to support cancer cell proliferation, making SHMT a promising target for the design and development of novel small-molecule antimetabolite chemotherapies. To advance structure-assisted drug design, knowledge of SHMT catalysis is crucial, but can only be fully realized when the atomic details of each reaction step governed by the acid-base catalysis are elucidated by visualizing active site hydrogen atoms.
View Article and Find Full Text PDFBiomacromolecules
September 2025
Department of Chemical Engineering, Columbia University, New York, New York 10027, United States.
Biomolecular condensates (BMCs) are central to subcellular organization, influencing processes from RNA metabolism to the stress response and amyloid pathologies. Despite their near ubiquity, we still do not fully understand how the primary sequence of biomolecules influences the formation and dynamics of condensates. Here, we examine how cationic amino acid identity shapes the properties of protein-RNA coacervates.
View Article and Find Full Text PDFNewton
August 2025
Department of Electrical and Computer Engineering, Boston University, Boston, MA, USA, 02215.
Hyperspectral imaging has been widely used for spectral and spatial identification of target molecules, yet often contaminated by sophisticated noise. Current denoising methods generally rely on independent and identically distributed noise statistics, showing corrupted performance for non-independent noise removal. Here, we demonstrate Self-supervised PErmutation Noise2noise Denoising (SPEND), a deep learning denoising architecture tailor-made for removing non-independent noise from a single hyperspectral image stack.
View Article and Find Full Text PDFChemical interface damping (CID), a plasmon decay mechanism arising from interfacial chemical perturbations, has become a crucial design parameter in surface-enhanced spectroscopic techniques and single-molecule biosensor development. Despite its significance, the mechanistic interplay between chiral molecular adsorption and CID remains poorly understood, especially for small biomolecules on plasmonic nanoparticles. In this study, we systematically investigated the CID responses of L/D-cysteine enantiomers on gold nanorods using single-particle dark-field spectroscopy.
View Article and Find Full Text PDFACS Omega
June 2025
Department of Organic and Macromolecular Chemistry, Ghent University, Krijgslaan 281-S4, 9000 Gent, Belgium.
In efforts to shed light on the complexity of biological processes, attaching several or different payloads onto a biomolecular target of interest has become an interesting tool within the field of bioconjugation. Herein, we report on the exploitation of prenylated (bio)-molecules in a 1,2,4-triazole-3,5-(4)-dione-based labeling strategy to develop a two-step single-site multiple labeling methodology that allows the introduction of up to three identical or different property-enhancing moieties. The methodology was first demonstrated on the small molecule targets farnesol and S-geranyl-2-thiouridine to be then applied to multi-(functional) labeling of amino acids and peptides.
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