In Vitro Microtubule and Motor Protein Motion on Glass
ORAL
Abstract
The intracellular microtubule associated protein kinesin uses adenosine triphosphate (ATP) as an energy source for unidirectional and processive motion on a microtubule filament. In a cell, kinesin motor proteins function as transporters for organelles, macromolecules and various particles. To study the related processes \textit{in vitro}, we have performed rhodamine-labeled microtubule gliding assays and kinesin-coated quantum dot motility assays on glass surfaces. Motility is observed by fluorescence microscopy. Results from these two assays, as well as the effect of ATP concentration on kinesin velocity will be presented. We will discuss how we use these assays for the manipulation of microtubules on a surface, thus enabling specific particle distribution by kinesin.
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Authors
A.L. Liao
WPI-Advanced Institute of Materials Research, Tohoku University, Japan and Materials Science and Engineering, Texas A\&M University
A. Sikora
WPI-Advanced Institute of Materials Research, Tohoku University, Japan
D. Oliveira
WPI-Advanced Institute of Materials Research, Tohoku University, Japan
K. Kim
WPI-Advanced Institute of Materials Research, Tohoku University, Japan
WPI-AIMR, Tohoku University, Japan
M. Umetsu
WPI-Advanced Institute of Materials Research, Tohoku University, Japan
T. Adschiri
WPI-Advanced Institute of Materials Research, Tohoku University, Japan
W. Hwang
Materials Science and Engineering; Department of Biomedical Engineering, Texas A\&M University
W. Teizer
WPI-Advanced Inst. of Materials Research, Tohoku University, Japan; Mat. Science and Engr. and Dept. of Physics and Astronomy, Texas A\&M University
WPI-AIMR, Tohoku University, Japan and Department of Physics and Astronomy, Texas A\&M University