Direct observation of the actin filament by tip-scan atomic force microscopy

• Published in: Microscopy Vol. 65; no. 4; p. 370
• Main Authors: Narita, Akihiro, Usukura, Eiji, Yagi, Akira, Tateyama, Kiyohiko, Akizuki, Shogo, Kikumoto, Mahito, Matsumoto, Tomoharu, Maéda, Yuichiro, Ito, Shuichi, Usukura, Jiro
• Format: Journal Article
• Language: English
• Published: England 01.08.2016
• Subjects: Actin Cytoskeleton - ultrastructure; Animals; Microscopy, Atomic Force - methods; Muscle, Skeletal - metabolism; Myosins - metabolism; Rabbits; Tropomyosin - metabolism; correlative microscopy; tropomyosin; atomic force microscopy; cytoskeleton; actin filament; tip-scan AFM
• ISSN: 2050-5701
• DOI: 10.1093/jmicro/dfw017

Actin filaments, the actin-myosin complex and the actin-tropomyosin complex were observed by a tip-scan atomic force microscope (AFM), which was recently developed by Olympus as the AFM part of a correlative microscope. This newly developed AFM uses cantilevers of similar size as stage-scan AFMs to improve substantially the spatial and temporal resolution. Such an approach has previously never been possible by a tip-scan system, in which a cantilever moves in the x, y and z directions. We evaluated the performance of this developed tip-scan AFM by observing the molecular structure of actin filaments and the actin-tropomyosin complex. In the image of the actin filament, the molecular interval of the actin subunits (∼5.5 nm) was clearly observed as stripes. From the shape of the stripes, the polarity of the actin filament was directly determined and the results were consistent with the polarity determined by myosin binding. In the image of the actin-tropomyosin complex, each tropomyosin molecule (∼2 nm in diameter) on the actin filament was directly observed without averaging images of different molecules. Each tropomyosin molecule on the actin filament has never been directly observed by AFM or electron microscopy. Thus, our developed tip-scan AFM offers significant potential in observing purified proteins and cellular structures at nanometer resolution. Current results represent an important step in the development of a new correlative microscope to observe nm-order structures at an acceptable frame rate (∼10 s/frame) by AFM at the position indicated by the fluorescent dye observed under a light microscope.