Atomic Force Microscopy-Based Force Spectroscopy and Multiparametric Imaging of Biomolecular and Cellular Systems

• Published in: Chemical reviews Vol. 121; no. 19; pp. 11701 - 11725
• Main Authors: Müller, Daniel J, Dumitru, Andra C, Lo Giudice, Cristina, Gaub, Hermann E, Hinterdorfer, Peter, Hummer, Gerhard, De Yoreo, James J, Dufrêne, Yves F, Alsteens, David
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 13.10.2021
• Subjects: atomic absorption spectrometry; Atomic force microscopy; force spectroscopy; functionalization; Image manipulation; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; Kinetics; Laboratories; Light microscopy; Lipids; Microscopes; Microscopy; Microscopy, Atomic Force - methods; molecules; Nucleic acids; Optical microscopy; peptides and proteins; Spectroscopy; Spectrum Analysis; Sugar; surface interactions; Temporal resolution; Thermodynamics; Tissues
• ISSN: 0009-2665; 1520-6890; 1520-6890
• DOI: 10.1021/acs.chemrev.0c00617

During the last three decades, a series of key technological improvements turned atomic force microscopy (AFM) into a nanoscopic laboratory to directly observe and chemically characterize molecular and cell biological systems under physiological conditions. Here, we review key technological improvements that have established AFM as an analytical tool to observe and quantify native biological systems from the micro- to the nanoscale. Native biological systems include living tissues, cells, and cellular components such as single or complexed proteins, nucleic acids, lipids, or sugars. We showcase the procedures to customize nanoscopic chemical laboratories by functionalizing AFM tips and outline the advantages and limitations in applying different AFM modes to chemically image, sense, and manipulate biosystems at (sub)­nanometer spatial and millisecond temporal resolution. We further discuss theoretical approaches to extract the kinetic and thermodynamic parameters of specific biomolecular interactions detected by AFM for single bonds and extend the discussion to multiple bonds. Finally, we highlight the potential of combining AFM with optical microscopy and spectroscopy to address the full complexity of biological systems and to tackle fundamental challenges in life sciences.