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      Intracellular production of hydrogels and synthetic RNA granules by multivalent enhancers

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          Abstract

          Non-membrane bound, hydrogel-like entities, such as RNA granules, nucleate essential cellular functions through their unique physico-chemical properties. However, these intracellular hydrogels have not been as extensively studied as their extracellular counterparts, primarily due to technical challenges in probing these materials in situ. Here, by taking advantage of a chemically inducible dimerization paradigm, we developed iPOLYMER, a strategy for rapid induction of protein-based hydrogels inside living cells. A series of biochemical and biophysical characterizations, in conjunction with computational modeling, revealed that the polymer network formed in the cytosol resembles a physiological hydrogel-like entity that behaves as a size-dependent molecular sieve. We studied several properties of the gel and functionalized it with RNA binding motifs that sequester polyadenine-containing nucleotides to synthetically mimic RNA granules. Therefore, we here demonstrate that iPOLYMER presents a unique and powerful approach to synthetically reconstitute hydrogel-like structures including RNA granules in intact cells.

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          Cell-free formation of RNA granules: bound RNAs identify features and components of cellular assemblies.

          Cellular granules lacking boundary membranes harbor RNAs and their associated proteins and play diverse roles controlling the timing and location of protein synthesis. Formation of such granules was emulated by treatment of mouse brain extracts and human cell lysates with a biotinylated isoxazole (b-isox) chemical. Deep sequencing of the associated RNAs revealed an enrichment for mRNAs known to be recruited to neuronal granules used for dendritic transport and localized translation at synapses. Precipitated mRNAs contain extended 3' UTR sequences and an enrichment in binding sites for known granule-associated proteins. Hydrogels composed of the low complexity (LC) sequence domain of FUS recruited and retained the same mRNAs as were selectively precipitated by the b-isox chemical. Phosphorylation of the LC domain of FUS prevented hydrogel retention, offering a conceptual means of dynamic, signal-dependent control of RNA granule assembly. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Micro- and macrorheology of mucus.

            Mucus is a complex biological material that lubricates and protects the human lungs, gastrointestinal (GI) tract, vagina, eyes, and other moist mucosal surfaces. Mucus serves as a physical barrier against foreign particles, including toxins, pathogens, and environmental ultrafine particles, while allowing rapid passage of selected gases, ions, nutrients, and many proteins. Its selective barrier properties are precisely regulated at the biochemical level across vastly different length scales. At the macroscale, mucus behaves as a non-Newtonian gel, distinguished from classical solids and liquids by its response to shear rate and shear stress, while, at the nanoscale, it behaves as a low viscosity fluid. Advances in the rheological characterization of mucus from the macroscopic to nanoscopic levels have contributed critical understanding to mucus physiology, disease pathology, and the development of drug delivery systems designed for use at mucosal surfaces. This article reviews the biochemistry that governs mucus rheology, the macro- and microrheology of human and laboratory animal mucus, rheological techniques applied to mucus, and the importance of an improved understanding of the physical properties of mucus to advancing the field of drug and gene delivery.
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              FG-rich repeats of nuclear pore proteins form a three-dimensional meshwork with hydrogel-like properties.

              Nuclear pore complexes permit rapid passage of cargoes bound to nuclear transport receptors, but otherwise suppress nucleocytoplasmic fluxes of inert macromolecules >/=30 kilodaltons. To explain this selectivity, a sieve structure of the permeability barrier has been proposed that is created through reversible cross-linking between Phe and Gly (FG)-rich nucleoporin repeats. According to this model, nuclear transport receptors overcome the size limit of the sieve and catalyze their own nuclear pore-passage by a competitive disruption of adjacent inter-repeat contacts, which transiently opens adjoining meshes. Here, we found that phenylalanine-mediated inter-repeat interactions indeed cross-link FG-repeat domains into elastic and reversible hydrogels. Furthermore, we obtained evidence that such hydrogel formation is required for viability in yeast.
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                Author and article information

                Journal
                101155473
                30248
                Nat Mater
                Nat Mater
                Nature materials
                1476-1122
                10 April 2018
                06 November 2017
                January 2018
                25 April 2018
                : 17
                : 1
                : 79-89
                Affiliations
                [1 ]Department of Cell Biology, School of Medicine, The Johns Hopkins University, Baltimore, MD, 21205
                [2 ]Center for Cell Dynamics, Institute for Basic Biomedical Sciences, The Johns Hopkins University, Baltimore, MD, 21205
                [3 ]Center for Imaging Science, Whitaker Biomedical Engineering Institute, The Johns Hopkins University, Baltimore, MD, 21218
                [4 ]Department of Biomedical Engineering, Whitaker Biomedical Engineering Institute, The Johns Hopkins University, Baltimore, MD 21218
                [5 ]Department of Biophysics and Biophysical Chemistry, School of Medicine, The Johns Hopkins University, Baltimore, MD, 21205
                [6 ]Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, MD, 21205
                [7 ]Department of Oncology, School of Medicine, Johns Hopkins University, Baltimore, MD, 21205
                Author notes
                []To whom general correspondence should be addressed: jctinoue@ 123456jhmi.edu (T.I.)
                []To whom correspondence regarding the computational analysis should be addressed: aas.afshar@ 123456gmail.com (A.S.A)
                [8]

                Current address: Department of Chemistry, National Taiwan University, Taiwan

                [*]

                These authors contributed equally.

                Article
                PMC5916848 PMC5916848 5916848 nihpa958180
                10.1038/nmat5006
                5916848
                29115293
                b8d9c5d6-5be0-41c1-b235-652e4acf5139
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