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      A Method for the Acute and Rapid Degradation of Endogenous Proteins

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          Summary

          Methods for the targeted disruption of protein function have revolutionized science and greatly expedited the systematic characterization of genes. Two main approaches are currently used to disrupt protein function: DNA knockout and RNA interference, which act at the genome and mRNA level, respectively. A method that directly alters endogenous protein levels is currently not available. Here, we present Trim-Away, a technique to degrade endogenous proteins acutely in mammalian cells without prior modification of the genome or mRNA. Trim-Away harnesses the cellular protein degradation machinery to remove unmodified native proteins within minutes of application. This rapidity minimizes the risk that phenotypes are compensated and that secondary, non-specific defects accumulate over time. Because Trim-Away utilizes antibodies, it can be applied to a wide range of target proteins using off-the-shelf reagents. Trim-Away allows the study of protein function in diverse cell types, including non-dividing primary cells where genome- and RNA-targeting methods are limited.

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          Highlights

          • Trim-Away is a widely applicable method to degrade endogenous proteins

          • Target proteins do not need to be modified before degradation

          • Proteins are degraded within minutes of application

          • Trim-Away allows efficient protein depletion in primary human cells

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          Most cited references44

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          Altering the genome by homologous recombination.

          M Capecchi (1989)
          Homologous recombination between DNA sequences residing in the chromosome and newly introduced, cloned DNA sequences (gene targeting) allows the transfer of any modification of the cloned gene into the genome of a living cell. This article discusses the current status of gene targeting with particular emphasis on germ line modification of the mouse genome, and describes the different methods so far employed to identify those rare embryonic stem cells in which the desired targeting event has occurred.
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            Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen.

            Small molecules that perturb specific protein functions are valuable tools for dissecting complex processes in mammalian cells. A combination of two phenotype-based screens, one based on a specific posttranslational modification, the other visualizing microtubules and chromatin, was used to identify compounds that affect mitosis. One compound, here named monastrol, arrested mammalian cells in mitosis with monopolar spindles. In vitro, monastrol specifically inhibited the motility of the mitotic kinesin Eg5, a motor protein required for spindle bipolarity. All previously known small molecules that specifically affect the mitotic machinery target tubulin. Monastrol will therefore be a particularly useful tool for studying mitotic mechanisms.
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              Critical role for NALP3/CIAS1/Cryopyrin in innate and adaptive immunity through its regulation of caspase-1.

              Mutations in the NALP3/CIAS1/cryopyrin gene are linked to three autoinflammatory disorders: Muckle-Wells syndrome, familial cold autoinflammatory syndrome, and chronic infantile neurologic cutaneous and articular syndrome. NALP3, with the adaptor molecule ASC, has been proposed to form a caspase-1-activating "inflammasome," a complex with pro-IL1beta-processing activity. Here, we demonstrate the effect of NALP3 deficiency on caspase-1 function. NALP3 was essential for the ATP-driven activation of caspase-1 in lipopolysaccharide-stimulated macrophages and for the efficient secretion of the caspase-1-dependent cytokines IL-1alpha, IL-1beta, and IL-18. IL-1beta has been shown to play a key role in contact hypersensitivity; we show that ASC- and NALP3-deficient mice also demonstrate an impaired contact hypersensitivity response to the hapten trinitrophenylchloride. NALP3, however, was not required for caspase-1 activation by Salmonella typhimurium, and NALP3 deficiency only partially protects mice from the lethal effects of endotoxin. These data suggest that NALP3 plays a specific role in the caspase-1 activation pathway.
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                Author and article information

                Contributors
                Journal
                Cell
                Cell
                Cell
                Cell Press
                0092-8674
                1097-4172
                14 December 2017
                14 December 2017
                : 171
                : 7
                : 1692-1706.e18
                Affiliations
                [1 ]Medical Research Council, Laboratory of Molecular Biology, Cambridge CB2 0QH, UK
                [2 ]Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany
                Author notes
                []Corresponding author dclift@ 123456mrc-lmb.cam.ac.uk
                [∗∗ ]Corresponding author lcj@ 123456mrc-lmb.cam.ac.uk
                [∗∗∗ ]Corresponding author melina.schuh@ 123456mpibpc.mpg.de
                [3]

                Lead Contact

                Article
                S0092-8674(17)31255-2
                10.1016/j.cell.2017.10.033
                5733393
                29153837
                464f0961-25f6-4847-8e1b-f02f1e2fdefb
                © 2017 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 2 June 2017
                : 2 October 2017
                : 19 October 2017
                Categories
                Article

                Cell biology
                protein degradation,protein knockdown,cell division,meiosis,primary cells,oocytes,macrophages,antibodies,rnai,crispr/cas9

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