High-Resolution Correlative Microscopy: Bridging the Gap between Single Molecule Localization Microscopy and Atomic Force Microscopy

التفاصيل البيبلوغرافية
العنوان: High-Resolution Correlative Microscopy: Bridging the Gap between Single Molecule Localization Microscopy and Atomic Force Microscopy
المؤلفون: Hendrik Deschout, Aleksandra Radenovic, Adrian P. Nievergelt, Michael W. Davidson, Lely Feletti, Pascal D. Odermatt, Georg E. Fantner, Radek Jankele, Arun Shivanandan
بيانات النشر: Amer Chemical Soc
مصطلحات موضوعية: Microscope, Materials science, Bioengineering, Nanotechnology, Context (language use), 02 engineering and technology, macromolecular substances, single molecule localization microscopy (SMLM), law.invention, 03 medical and health sciences, Live cell imaging, law, Microscopy, General Materials Science, Photoactivated localization microscopy, 030304 developmental biology, chemistry.chemical_classification, 0303 health sciences, Mechanical Engineering, Biomolecule, technology, industry, and agriculture, direct stochastic optical reconstruction microscopy (dSTORM), General Chemistry, 021001 nanoscience & nanotechnology, Condensed Matter Physics, Characterization (materials science), live cell imaging, chemistry, correlative imaging photoactivated localization microscopy (PALM), Atomic force microscopy (AFM), Scanning ion-conductance microscopy, 0210 nano-technology
الوصف: Nanoscale characterization of living samples has become essential for modern biology. Atomic force microscopy (AFM) creates topological images of fragile biological structures from biomolecules to living cells in aqueous environments. However, correlating nanoscale structure to biological function of specific proteins can be challenging. To this end we have built and characterized a correlated single molecule localization microscope (SMLM)/AFM that allows localizing specific, labeled proteins within high-resolution AFM images in a biologically relevant context. Using direct stochastic optical reconstruction microscopy (dSTORM)/AFM, we directly correlate and quantify the density of localizations with the 3D topography using both imaging modalities along (F-)actin cytoskeletal filaments. In addition, using photo activated light microscopy (PALM)/AFM, we provide correlative images of bacterial cells in aqueous conditions. Moreover, we report the first correlated AFM/PALM imaging of live mammalian cells. The complementary information provided by the two techniques opens a new dimension for structural and functional nanoscale biology.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1070ab5aae55762b6dd60f7370047b89Test
https://infoscience.epfl.ch/record/209947Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....1070ab5aae55762b6dd60f7370047b89
قاعدة البيانات: OpenAIRE