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      Standardized Nanomechanical Atomic Force Microscopy Procedure (SNAP) for Measuring Soft and Biological Samples

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          Abstract

          We present a procedure that allows a reliable determination of the elastic (Young’s) modulus of soft samples, including living cells, by atomic force microscopy (AFM). The standardized nanomechanical AFM procedure (SNAP) ensures the precise adjustment of the AFM optical lever system, a prerequisite for all kinds of force spectroscopy methods, to obtain reliable values independent of the instrument, laboratory and operator. Measurements of soft hydrogel samples with a well-defined elastic modulus using different AFMs revealed that the uncertainties in the determination of the deflection sensitivity and subsequently cantilever’s spring constant were the main sources of error. SNAP eliminates those errors by calculating the correct deflection sensitivity based on spring constants determined with a vibrometer. The procedure was validated within a large network of European laboratories by measuring the elastic properties of gels and living cells, showing that its application reduces the variability in elastic moduli of hydrogels down to 1%, and increased the consistency of living cells elasticity measurements by a factor of two. The high reproducibility of elasticity measurements provided by SNAP could improve significantly the applicability of cell mechanics as a quantitative marker to discriminate between cell types and conditions.

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          Most cited references33

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          Atomic Force Microscope

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            Local force and geometry sensing regulate cell functions.

            The shapes of eukaryotic cells and ultimately the organisms that they form are defined by cycles of mechanosensing, mechanotransduction and mechanoresponse. Local sensing of force or geometry is transduced into biochemical signals that result in cell responses even for complex mechanical parameters such as substrate rigidity and cell-level form. These responses regulate cell growth, differentiation, shape changes and cell death. Recent tissue scaffolds that have been engineered at the micro- and nanoscale level now enable better dissection of the mechanosensing, transduction and response mechanisms.
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              The optical stretcher: a novel laser tool to micromanipulate cells.

              When a dielectric object is placed between two opposed, nonfocused laser beams, the total force acting on the object is zero but the surface forces are additive, thus leading to a stretching of the object along the axis of the beams. Using this principle, we have constructed a device, called an optical stretcher, that can be used to measure the viscoelastic properties of dielectric materials, including biologic materials such as cells, with the sensitivity necessary to distinguish even between different individual cytoskeletal phenotypes. We have successfully used the optical stretcher to deform human erythrocytes and mouse fibroblasts. In the optical stretcher, no focusing is required, thus radiation damage is minimized and the surface forces are not limited by the light power. The magnitude of the deforming forces in the optical stretcher thus bridges the gap between optical tweezers and atomic force microscopy for the study of biologic materials.
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                Author and article information

                Contributors
                radmacher@uni-bremen.de
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                11 July 2017
                11 July 2017
                2017
                : 7
                : 5117
                Affiliations
                [1 ]ISNI 0000 0001 2172 9288, GRID grid.5949.1, Institute of Physiology II, , University of Münster, ; 48149 Münster, Germany
                [2 ]ISNI 0000 0001 2297 4381, GRID grid.7704.4, Institute of Biophysics, , University of Bremen, ; 28359 Bremen, Germany
                [3 ]ISNI 0000 0004 1937 0247, GRID grid.5841.8, Institute for Bioengineering of Catalonia, , University of Barcelona, and CIBER Enfermedades Respiratorias, ; 08028 Barcelona, Spain
                [4 ]ISNI 0000 0004 0576 5395, GRID grid.11047.33, Department of Mechanical Engineering & Aeronautics, , University of Patras, ; 265 04 Patras, Greece
                [5 ]ISNI 0000 0001 1958 0162, GRID grid.413454.3, Institute of Nuclear Physics, , Polish Academy of Sciences, ; PL-31342 Krakow, Poland
                [6 ]ISNI 0000 0004 0625 9726, GRID grid.452504.2, , Instituto de Ciencia de Materiales de Madrid, ; CSIC, Sor Juana Ines de la Cruz 3, 28049 Madrid, Spain
                [7 ]ISNI 0000 0001 2159 9858, GRID grid.8970.6, CMPI-CIIL, CNRS UMR 8204 - INSERM U1019, , Institut Pasteur de Lille - Univ Lille, ; F-59019 Lille, Cedex France
                [8 ]ISNI 0000 0001 2176 4817, GRID grid.5399.6, BIAM, CEA, , Aix-Marseille Univ., ; Saint-Paul-Lez-Durance, 13108 France
                [9 ]CEA Marcoule, iBEB, Department of Biochemistry and Nuclear Toxicology, F-30207 Bagnols-sur-Cèze, France
                [10 ]ISNI 0000 0004 1757 2822, GRID grid.4708.b, CIMaINa and Department of Physics, , Università degli Studi di Milano, ; via Celoria 16, 20133 Milano, Italy
                [11 ]ISNI 0000 0001 0472 9649, GRID grid.263488.3, College of Materials Science and Engineering, Shenzhen Key Laboratory of Polymer Science and Technology, Guangdong Research Center for Interfacial Engineering of Functional Materials, Nanshan District Key Lab for Biopolymers and Safety Evaluation, , Shenzhen University, ; Shenzhen, 518060 PR China
                [12 ]ISNI 0000 0001 0472 9649, GRID grid.263488.3, College of Optoelectronic Engineering, Key Laboratory of Optoelectronic Devices and System of Ministry of Education and Guangdong Province, , Shenzhen University, ; Shenzhen, 518060 PR China
                [13 ]ISNI 0000 0001 2176 4817, GRID grid.5399.6, U1006 INSERM, , Aix-Marseille Université, Parc Scientifique et Technologique de Luminy, ; 13009 Marseille, France
                [14 ]ISNI 000000041936877X, GRID grid.5386.8, , Department of Physiology and Biophysics, Weill Cornell Medicine, ; New York, NY 10065 USA
                [15 ]ISNI 000000041936877X, GRID grid.5386.8, , Department of Anesthesiology, Weill Cornell Medicine, ; New York, NY 10065 USA
                [16 ]ICSM, UMR 5257, CEA, CNRS, ENSCM, Univ. Montpellier, Site de Marcoule, Bât. 426, BP 17171, 30207 Bagnols-sur-Cèze, France
                [17 ]Univ. Grenoble Alpes, CEA, CNRS, IBS, F-38000 Grenoble, France
                Author information
                http://orcid.org/0000-0002-4169-6679
                http://orcid.org/0000-0001-8668-2580
                http://orcid.org/0000-0002-7757-8340
                http://orcid.org/0000-0001-8744-4541
                Article
                5383
                10.1038/s41598-017-05383-0
                5505948
                28127051
                f937ca7b-dcd5-45bd-9b7a-34553670e213
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 January 2017
                : 26 May 2017
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