Living cells contain a range of densely phosphorylated surfaces, including phospholipid membranes, ribonucleoproteins, and nucleic acid polymers. Hyperphosphorylated surfaces also accumulate in neurodegenerative diseases as neurofibrillar tangles. We have synthesized and structurally characterized a precisely patterned phosphotyrosine surface and establish this assembly as a surrogate of the neuronal tangles by demonstrating its high-affinity binding to histone H1. This association with nucleic acid binding proteins underscores the role such hyperphosphorylated surfaces may play in disease and opens functional exploration into protein-phosphorylated surface interactions in a wide range of other complex assemblies.
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J Mater Chem B
November 2024
Department of Chemistry, Brandeis University, 415 South St., Waltham, MA 02453, USA.
Cell spheroids, including organoids, serve as a valuable link between systems and animal models, offering powerful tools for studying cell biology in a three-dimensional environment. However, existing methods for generating cell spheroids are time consuming or difficult to scale up for large-scale production. Our recent study has revealed that transcytotic peptide assemblies, which transform from nanoparticles to nanofibers by enzymatic reactions, can create an intercellular fibril/gel, accelerating cell spheroid formation from a 2D cell culture or a cell suspension.
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Department of Physics, São Paulo State University (UNESP), Institute of Biosciences, Humanities and Exact Sciences, Sao Jose do Rio Preto, 15054-000, SP, Brazil; Multiuser Center for Biomolecular Innovation (CMIB), São Paulo State University (UNESP), Institute of Biosciences, Humanities and Exact Sciences, Sao Jose do Rio Preto, 15054-000, SP, Brazil. Electronic address:
The Growth factor receptor-bound protein 2 (Grb2) participates in early signaling complexes and regulates tyrosine kinase-mediated signal transduction through a monomer-dimer equilibrium. Grb2 dimeric state inhibits signal transduction whereas the monomer promotes signaling downstream. Since Grb2 dimer K is ∼0.
View Article and Find Full Text PDFSci Rep
May 2024
Division of Biomedical Sciences, Faculty of Medicine, Memorial University, St. John's, NL, A1B 3V6, Canada.
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May 2024
Meyer Cancer Center, Weill Cornell Medicine, New York, NY, USA.
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View Article and Find Full Text PDFJ Vis Exp
January 2024
School of Life Sciences, SUSTech University;
Visualization of proteins in living cells using GFP (Green Fluorescent Protein) and other fluorescent tags has greatly improved understanding of protein localization, dynamics, and function. Compared to immunofluorescence, live imaging more accurately reflects protein localization without potential artifacts arising from tissue fixation. Importantly, live imaging enables quantitative and temporal characterization of protein levels and localization, crucial for understanding dynamic biological processes such as cell movement or division.
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