Paper
19 November 2001 Controlling actin motility on microfabricated linear channels
Chitladda Mahanivong, Jonathan P. Wright, Murat Kekic, Duy K. Pham, Cristobal dos Remedios, Dan V. Nicolau
Author Affiliations +
Proceedings Volume 4590, BioMEMS and Smart Nanostructures; (2001) https://doi.org/10.1117/12.454621
Event: International Symposium on Microelectronics and MEMS, 2001, Adelaide, Australia
Abstract
Heavy meromyosin (HMM), a proteolytically cleaved derivative of myosin has previously been shown to interact with actin in well-established in vitro motility assays on nitrocellulose surfaces. In this study, the assays were conducted to demonstrate that the motility of actin filaments is confined in the micron-sized channels fabricated via laser ablation in a layer of the photosensitive resist polymer (O-acryloyloxime acetophenone oxime, AAPO). A solution containing myosin labelled with fluorophore 5-iodoacetamidofluorescein (5-IAF) was applied to the microfabricated AAPO surface and shown to bind specifically to the micron-size channels. In the motility assay, HMM, rhodamine-phalloidin labelled actin and ATP were sequentially added and the movement of the actin filaments was observed by fluorescence microscopy and recorded with a CCD camera. The experiments prove that although the actin filaments show an only-partial propensity for attachment in myosin-rich areas, their motility is confined to a large extent in micro- channels.
© (2001) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Chitladda Mahanivong, Jonathan P. Wright, Murat Kekic, Duy K. Pham, Cristobal dos Remedios, and Dan V. Nicolau "Controlling actin motility on microfabricated linear channels", Proc. SPIE 4590, BioMEMS and Smart Nanostructures, (19 November 2001); https://doi.org/10.1117/12.454621
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KEYWORDS
Proteins

Microfabrication

Polymers

Laser ablation

In vitro testing

CCD cameras

Luminescence

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