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      openFrame: A modular, sustainable, open microscopy platform with single‐shot, dual‐axis optical autofocus module providing high precision and long range of operation

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          Abstract

          openFrame’ is a modular, low‐cost, open‐hardware microscopy platform that can be configured or adapted to most light microscopy techniques and is easily upgradeable or expandable to multiple modalities. The ability to freely mix and interchange both open‐source and proprietary hardware components or software enables low‐cost, yet research‐grade instruments to be assembled and maintained. It also enables rapid prototyping of advanced or novel microscope systems. For long‐term time‐lapse image data acquisition, slide‐scanning or high content analysis, we have developed a novel optical autofocus incorporating orthogonal cylindrical optics to provide robust single‐shot closed‐loop focus lock, which we have demonstrated to accommodate defocus up to ±37 μm with <200 nm accuracy, and a two‐step autofocus mode which we have shown can operate with defocus up to ±68 μm. We have used this to implement automated single molecule localisation microscopy (SMLM) in a relatively low‐cost openFrame‐based instrument using multimode diode lasers for excitation and cooled CMOS cameras.

          LAY DESCRIPTION

          We present a modular, low‐cost, microscopy platform called ‘ openFrame’ that can be configured or adapted to most light microscopy techniques and is easily upgradeable. openFrame‐based microscopes are designed to be used with open‐source software tools and low‐cost/self‐built hardware components, such that cost‐effective instruments can be assembled and maintained locally by skilled users instead of requiring visits from service engineers. The core openFrame hardware components can be fabricated using freely shared CAD files or they can be purchased by users to implement a wide range of instruments, which can utilise a mixture of open and proprietary hardware components as desired. We intend this platform to widen access to basic and advanced microscopy techniques, including in lower‐resource settings. We also expect it to be useful to researchers prototyping new microscopes, since it allows a core instrument to be rapidly assembled and then easily modified with minimal constraints, for example, from proprietary software or legacy design choices. The flexibility to reconfigure openFrame‐based microscopes and interchange/recycle components between different instruments reduces obsolescence. The openFrame‐based microscope presented here includes a novel open‐source optical autofocus unit ( openAF) that may be useful for long‐term time‐lapse imaging, and in slide‐scanning or automated multiwell plate microscopes. We demonstrate the use of an openFrame‐based instrument for super‐resolved microscopy using single molecule localisation microscopy (SMLM) utilising low‐cost cooled CMOS cameras and multimode diode lasers for high power excitation.

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          Most cited references32

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          NIH Image to ImageJ: 25 years of image analysis

          For the past twenty five years the NIH family of imaging software, NIH Image and ImageJ have been pioneers as open tools for scientific image analysis. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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            Advanced methods of microscope control using μManager software.

            μManager is an open-source, cross-platform desktop application, to control a wide variety of motorized microscopes, scientific cameras, stages, illuminators, and other microscope accessories. Since its inception in 2005, μManager has grown to support a wide range of microscopy hardware and is now used by thousands of researchers around the world. The application provides a mature graphical user interface and offers open programming interfaces to facilitate plugins and scripts. Here, we present a guide to using some of the recently added advanced μManager features, including hardware synchronization, simultaneous use of multiple cameras, projection of patterned light onto a specimen, live slide mapping, imaging with multi-well plates, particle localization and tracking, and high-speed imaging.
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              Super-resolution microscopy with DNA-PAINT

              In DNA-PAINT, transient binding of dye-labeled oligonucleotides to their target strands creates the ‘blinking’ required for stochastic nanoscopy. This protocol describes how to apply DNA-PAINT, from sample preparation to data processing.
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                Author and article information

                Contributors
                jonathan.lightley13@imperial.ac.uk
                Journal
                J Microsc
                J Microsc
                10.1111/(ISSN)1365-2818
                JMI
                Journal of Microscopy
                John Wiley and Sons Inc. (Hoboken )
                0022-2720
                1365-2818
                27 September 2023
                November 2023
                : 292
                : 2 ( doiID: 10.1111/jmi.v292.2 )
                : 64-77
                Affiliations
                [ 1 ] Photonics Group, Physics Department Imperial College London London UK
                [ 2 ] Francis Crick Institute London UK
                [ 3 ] Department of Surgery and Cancer Imperial College London London UK
                [ 4 ] Cairn Research Ltd Faversham Kent England
                [ 5 ] Leibniz‐Forschungsinstitut für Molekulare Pharmakologie Berlin Germany
                [ 6 ] Department of Inflammation and Immunology Imperial College London London UK
                Author notes
                [*] [* ] Correspondence

                J. Lightley, Photonics Group, Physics Department, Imperial College London, London SW7 2AZ, UK.

                Email: jonathan.lightley13@ 123456imperial.ac.uk

                Author information
                https://orcid.org/0000-0003-4527-8578
                https://orcid.org/0000-0001-6253-2836
                https://orcid.org/0000-0001-9190-0407
                https://orcid.org/0000-0003-4965-9669
                https://orcid.org/0000-0003-3084-6595
                https://orcid.org/0000-0002-0478-6755
                Article
                JMI13219
                10.1111/jmi.13219
                10953376
                37616077
                3c22ea32-a5c0-4a3e-815b-25aeda611543
                © 2023 The Authors. Journal of Microscopy published by John Wiley & Sons Ltd on behalf of Royal Microscopical Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 04 August 2023
                : 18 April 2023
                : 21 August 2023
                Page count
                Figures: 7, Tables: 0, Pages: 14, Words: 8960
                Funding
                Funded by: Biotechnology and Biological Sciences Research Council , doi 10.13039/501100000268;
                Award ID: BBSRC EP/R511547/1
                Funded by: Engineering and Physical Sciences Research Council , doi 10.13039/501100000266;
                Award ID: EPSRC EP/R511547/1
                Funded by: Cancer Research UK , doi 10.13039/501100000289;
                Award ID: A28450
                Award ID: FC001003
                Award ID: A29368
                Funded by: Chan Zuckerber Initiative DAF, an advised fund of Silicon Valley Community Foundation
                Award ID: 2021–234618
                Award ID: 2023–321240
                Funded by: UK Medical Research Council
                Award ID: FC001003
                Funded by: Wellcome Trust , doi 10.13039/100010269;
                Award ID: FC001003
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                November 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.9 mode:remove_FC converted:20.03.2024

                Microscopy & Imaging
                autofocus,fluorescence microscopy,open‐source microscopy,superresolution,sustainability,widening participation

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