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      Cell-free biosensors for rapid detection of water contaminants

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          Abstract

          Access to safe drinking water is a global problem, and methods to reliably and easily detect contaminants could be transformative. We report the development of a cell-free in vitro transcription system that uses RNA output sensors activated by ligand induction (ROSALIND) to detect contaminants in water. A combination of highly processive RNA polymerases, allosteric protein transcription factors and synthetic DNA transcription templates regulates the synthesis of a fluorescence-activating RNA aptamer. The presence of a target contaminant induces the transcription of the aptamer, and a fluorescent signal is produced. We apply ROSALIND to detect a range of water contaminants, including antibiotics, small molecules and metals. We also show that adding RNA circuitry can invert responses, reduce crosstalk and improve sensitivity without protein engineering. The ROSALIND system can be freeze-dried for easy storage and distribution, and we apply it in the field to test municipal water supplies, demonstrating its potential utility for monitoring water quality.

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          Most cited references52

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          CRISPR-Cas12a target binding unleashes indiscriminate single-stranded DNase activity

          CRISPR-Cas12a (Cpf1) proteins are RNA-guided enzymes that bind and cut DNA as components of bacterial adaptive immune systems. Like CRISPR-Cas9, Cas12a has been harnessed for genome editing based on its ability to generate targeted, double-stranded DNA (dsDNA) breaks. Here we show that RNA-guided DNA binding unleashes indiscriminate single-stranded DNA (ssDNA) cleavage activity by Cas12a that completely degrades ssDNA molecules. We find that target-activated, non-specific ssDNase cleavage is also a property of other type V CRISPR-Cas12 enzymes. By combining Cas12a ssDNase activation with isothermal amplification, we create a method termed DNA Endonuclease Targeted CRISPR Trans Reporter (DETECTR), which achieves attomolar sensitivity for DNA detection. DETECTR enables rapid and specific detection of human papillomavirus in patient samples, thereby providing a simple platform for molecular diagnostics.
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            Multiplexed and portable nucleic acid detection platform with Cas13, Cas12a, and Csm6

            Rapid detection of nucleic acids is integral for clinical diagnostics and biotechnological applications. We recently developed a platform termed SHERLOCK (Specific High Sensitivity Enzymatic Reporter UnLOCKing) that combines isothermal pre-amplification with Cas13 to detect single molecules of RNA or DNA. Through characterization of CRISPR enzymology and application development, we report here four advances integrated into SHERLOCKv2: 1) 4-channel single reaction multiplexing using orthogonal CRISPR enzymes; 2) quantitative measurement of input down to 2 aM; 3) 3.5-fold increase in signal sensitivity by combining Cas13 with Csm6, an auxilary CRISPR-associated enzyme; and 4) lateral flow read-out. SHERLOCKv2 can detect Dengue or Zika virus ssRNA as well as mutations in patient liquid biopsy samples via lateral flow, highlighting its potential as a multiplexable, portable, rapid, and quantitative detection platform of nucleic acids.
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              Global threats to human water security and river biodiversity.

              Protecting the world's freshwater resources requires diagnosing threats over a broad range of scales, from global to local. Here we present the first worldwide synthesis to jointly consider human and biodiversity perspectives on water security using a spatial framework that quantifies multiple stressors and accounts for downstream impacts. We find that nearly 80% of the world's population is exposed to high levels of threat to water security. Massive investment in water technology enables rich nations to offset high stressor levels without remedying their underlying causes, whereas less wealthy nations remain vulnerable. A similar lack of precautionary investment jeopardizes biodiversity, with habitats associated with 65% of continental discharge classified as moderately to highly threatened. The cumulative threat framework offers a tool for prioritizing policy and management responses to this crisis, and underscores the necessity of limiting threats at their source instead of through costly remediation of symptoms in order to assure global water security for both humans and freshwater biodiversity.
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                Author and article information

                Journal
                9604648
                20305
                Nat Biotechnol
                Nat Biotechnol
                Nature biotechnology
                1087-0156
                1546-1696
                22 May 2020
                06 July 2020
                December 2020
                06 January 2021
                : 38
                : 12
                : 1451-1459
                Affiliations
                [1 – ]Department of Chemical and Biological Engineering, Northwestern University (Evanston IL, USA)
                [2 – ]Center for Synthetic Biology, Northwestern University (Evanston, IL, USA)
                [3 – ]Center for Water Research, Northwestern University (Evanston, IL, USA)
                [4 – ]Interdisciplinary Biological Sciences Graduate Program, Northwestern University (Evanston, IL, USA)
                [5 – ]Department of Chemistry, Indiana University, (Bloomington, IN, USA)
                [6 – ]Department of Civil and Environmental Engineering, Northwestern University (Evanston, IL, USA)
                [7 – ]Department of Biological Engineering, Massachusetts Institute of Technology (Cambridge, MA, USA)
                [8 – ]Department of Chemical Engineering, Pohang University of Science and Technology (Pohang, Republic of Korea)
                [9 – ]Wyss Institute for Biologically Inspired Engineering, Harvard University (Boston, MA, USA)
                [10 – ]Departmento de Ingeniería Hidráulica y Ambiental, Pontificia Universidad Católica de Chile (Santiago, Chile)
                [11 – ]Centro de Desarrollo Urbano Sustentable (CEDEUS) (Santiago, Chile)
                [12 – ]Department of Geological and Environmental Sciences, California State University, Chico (Chico, CA, USA)
                [13 – ]Center for Water and the Environment, California State University, Chico (Chico, CA, USA)
                [14 – ]Department of Molecular and Cellular Biochemistry, Indiana University, (Bloomington, IN, USA)
                [15 – ]Institute for Medical Engineering & Science, Massachusetts Institute of Technology (Cambridge, MA, USA)
                [16 – ]Synthetic Biology Center, Massachusetts Institute of Technology (Cambridge, MA, USA)
                [17 – ]Broad Institute of MIT and Harvard (Cambridge, MA, USA)
                Author notes
                [*]

                These authors contributed equally

                AUTHOR CONTRIBUTIONS

                Conceptualization, J.K.J., K.K.A., J.J.C & J.B.L.; Data curation, J.K.J., K.K.A., M.S.V. & J.B.L.; Formal analysis, J.K.J., K.K.A. & J.B.L.; Funding acquisition, J.B.L., J.-F.G., D.P.G., P.A.P.; Investigation, J.K.J., K.K.A., M.S.V., M.D., P.R.C., J.W.L., J.-F.G.; Methodology, J.K.J., K.K.A., M.S.V., J.W.L., P.Q.N., D.A.C., M.D., S.M., J.-F.G., & J.B.L.; Project administration, J.K.J., K.K.A. & J.B.L.; Resources, D.A.C., D.P.G., P.A.P., S.M.; Supervision, J.K.J, K.K.A, J.J.C. & J.B.L; Validation, J.K.J., K.K.A., M.S.V., M.D., P.R.C., J.-F.G.; Visualization, J.K.J., K.K.A. & J.B.L.; Writing – original draft, J.K.J, K.K.A. & J.B.L.; Writing – review & editing, J.K.J., K.K.A., M.S.V., M.D., P.R.C., J.W.L., P.Q.N., D.A.C., P.A.P., S.M., J.-F.G., D.P.G., J.J.C. & J.B.L.; J.K.J. and K.K.A. contributed equally to this work.

                Article
                NIHMS1596286
                10.1038/s41587-020-0571-7
                7718425
                32632301
                18fd66a4-2dab-4c56-b02b-cb428f221ea4

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                Biotechnology
                Biotechnology

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