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      A human apolipoprotein L with detergent-like activity kills intracellular pathogens

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          Abstract

          Activation of cell-autonomous defense by the immune cytokine interferon-γ (IFN-γ) is critical to the control of life-threatening infections in humans. IFN-γ induces the expression of hundreds of host proteins in all nucleated cells and tissues, yet many of these proteins remain uncharacterized. We screened 19,050 human genes by CRISPR-Cas9 mutagenesis and identified IFN-γ–induced apolipoprotein L3 (APOL3) as a potent bactericidal agent protecting multiple non–immune barrier cell types against infection. Canonical apolipoproteins typically solubilize mammalian lipids for extracellular transport; APOL3 instead targeted cytosol-invasive bacteria to dissolve their anionic membranes into human-bacterial lipoprotein nanodiscs detected by native mass spectrometry and visualized by single-particle cryo–electron microscopy. Thus, humans have harnessed the detergent-like properties of extracellular apolipoproteins to fashion an intracellular lysin, thereby endowing resident nonimmune cells with a mechanism to achieve sterilizing immunity.

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          Most cited references62

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          UCSF Chimera--a visualization system for exploratory research and analysis.

          The design, implementation, and capabilities of an extensible visualization system, UCSF Chimera, are discussed. Chimera is segmented into a core that provides basic services and visualization, and extensions that provide most higher level functionality. This architecture ensures that the extension mechanism satisfies the demands of outside developers who wish to incorporate new features. Two unusual extensions are presented: Multiscale, which adds the ability to visualize large-scale molecular assemblies such as viral coats, and Collaboratory, which allows researchers to share a Chimera session interactively despite being at separate locales. Other extensions include Multalign Viewer, for showing multiple sequence alignments and associated structures; ViewDock, for screening docked ligand orientations; Movie, for replaying molecular dynamics trajectories; and Volume Viewer, for display and analysis of volumetric data. A discussion of the usage of Chimera in real-world situations is given, along with anticipated future directions. Chimera includes full user documentation, is free to academic and nonprofit users, and is available for Microsoft Windows, Linux, Apple Mac OS X, SGI IRIX, and HP Tru64 Unix from http://www.cgl.ucsf.edu/chimera/. Copyright 2004 Wiley Periodicals, Inc.
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            MotionCor2: anisotropic correction of beam-induced motion for improved cryo-electron microscopy

            MotionCor2 software corrects for beam-induced sample motion, improving the resolution of cryo-EM reconstructions.
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              The Phyre2 web portal for protein modeling, prediction and analysis.

              Phyre2 is a suite of tools available on the web to predict and analyze protein structure, function and mutations. The focus of Phyre2 is to provide biologists with a simple and intuitive interface to state-of-the-art protein bioinformatics tools. Phyre2 replaces Phyre, the original version of the server for which we previously published a paper in Nature Protocols. In this updated protocol, we describe Phyre2, which uses advanced remote homology detection methods to build 3D models, predict ligand binding sites and analyze the effect of amino acid variants (e.g., nonsynonymous SNPs (nsSNPs)) for a user's protein sequence. Users are guided through results by a simple interface at a level of detail they determine. This protocol will guide users from submitting a protein sequence to interpreting the secondary and tertiary structure of their models, their domain composition and model quality. A range of additional available tools is described to find a protein structure in a genome, to submit large number of sequences at once and to automatically run weekly searches for proteins that are difficult to model. The server is available at http://www.sbg.bio.ic.ac.uk/phyre2. A typical structure prediction will be returned between 30 min and 2 h after submission.
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                Author and article information

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                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                July 15 2021
                July 16 2021
                July 15 2021
                July 16 2021
                : 373
                : 6552
                : eabf8113
                Affiliations
                [1 ]Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.
                [2 ]Yale Systems Biology Institute, West Haven, CT 06477, USA.
                [3 ]Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06510, USA.
                [4 ]Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06510, USA.
                [5 ]Yale Nanobiology Institute, West Haven, CT 06477, USA.
                [6 ]Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA.
                [7 ]Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Melbourne 3800, Australia.
                [8 ]Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06510, USA.
                [9 ]Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06510, USA.
                [10 ]Saints-Pères Paris Institute for the Neurosciences, Centre National de la Recherche Scientifique (CNRS), Université de Paris, F-75006 Paris, France.
                Article
                10.1126/science.abf8113
                34437126
                d3ed0fe9-d27f-4928-8c1d-e16167865764
                © 2021

                https://www.sciencemag.org/about/science-licenses-journal-article-reuse

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