4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      On Some Current Challenges in High-Resolution Optical Bioimaging

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          In this Perspective we propose our current point of view and a suggestive roadmap on the field of high-resolution optical microscopy dedicated to bioimaging. Motivated by biological applications, researchers have indeed devised an impressive amount of strategies to address the diverse constraints of imaging and studying biological matter down to the molecular scale, making this interdisciplinary research field a vibrant forum for creativity. Throughout the discussion, we highlight several striking recent successes in this quest. We also identify some next challenges still ahead to apprehend biological questions in increasingly complex living organisms for integrative studies in a minimally invasive manner.

          Related collections

          Most cited references74

          • Record: found
          • Abstract: found
          • Article: not found

          Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

          We have developed a high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores. In each imaging cycle, only a fraction of the fluorophores were turned on, allowing their positions to be determined with nanometer accuracy. The fluorophore positions obtained from a series of imaging cycles were used to reconstruct the overall image. We demonstrated an imaging resolution of 20 nm. This technique can, in principle, reach molecular-scale resolution.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Imaging intracellular fluorescent proteins at nanometer resolution.

            We introduce a method for optically imaging intracellular proteins at nanometer spatial resolution. Numerous sparse subsets of photoactivatable fluorescent protein molecules were activated, localized (to approximately 2 to 25 nanometers), and then bleached. The aggregate position information from all subsets was then assembled into a superresolution image. We used this method--termed photoactivated localization microscopy--to image specific target proteins in thin sections of lysosomes and mitochondria; in fixed whole cells, we imaged vinculin at focal adhesions, actin within a lamellipodium, and the distribution of the retroviral protein Gag at the plasma membrane.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Near-infrared fluorophores for biomedical imaging

                Bookmark

                Author and article information

                Journal
                ACS Photonics
                ACS Photonics
                ph
                apchd5
                ACS Photonics
                American Chemical Society
                2330-4022
                26 July 2022
                17 August 2022
                : 9
                : 8
                : 2538-2546
                Affiliations
                []Laboratoire Photonique Numérique et Nanosciences, University of Bordeaux , F-33400 Talence, France
                []LP2N UMR 5298, Institut d’Optique Graduate School, CNRS , F-33400 Talence, France
                Author notes
                Author information
                https://orcid.org/0000-0002-3573-5387
                Article
                10.1021/acsphotonics.2c00606
                9389608
                35996373
                6c74f01b-eb6c-42b8-a2b3-5b34b483f757
                © 2022 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                Funding
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 848645
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 951294
                Categories
                Perspective
                Custom metadata
                ph2c00606
                ph2c00606

                optical bioimaging,biophotonics,super-resolution microscopy,optical microscopy,label-free imaging,fluorescence microscopy

                Comments

                Comment on this article