Functional Expression of Prestin, the Outer Hair Cell Motor Protein, Using the Baculovirus/Insect Cell System

Journal of Biomechanical Science and Engineering

Izumi KUMAGAI¹  Takashi TADENUMA⁵  Toshimitsu KOBAYASHI²  Shun KUMANO⁵  Hiroshi WADA⁵  Michio MURAKOSHI⁵  Kouhei TSUMOTO⁴  Katsuhisa IKEDA³  Koji IIDA⁵ 

[1] Department of Biomolecular Engineering, Tohoku University;Department of Otorhinolaryngology, Tohoku University, Graduate School of Medicine;Department of Otorhinolaryngology, Juntendo University School of Medicine;Department of Medical Genome Sciences, The University of Tokyo;Department of Bioengineering and Robotics, Tohoku University

关键词: Outer Hair Cell;    Prestin;    Membrane Protein Expression;    Baculovirus;    Sf9 Insect Cell;    Patch-Clamp Technique;    Nonlinear Capacitance;    Western Blotting;   

DOI  :  10.1299/jbse.3.287

来源: Japan Society of Mechanical Engineers

【 摘 要 】

References(28)A source of the electromotility of the outer hair cells (OHCs), which enables the high sensitivity of mammalian hearing, is believed to be voltage-dependent conformational change of the motor protein prestin embedded in the lateral wall of the OHCs. As a result of extensive studies on this unique motor protein using prestin-expressing cells, knowledge about its structure and function has been gradually accumulated. To obtain further knowledge about prestin, research using purified prestin molecules is necessary, and thus a method for efficiently obtaining prestin molecules is required. In the present study, construction of an expression system for prestin using the baculovirus/Sf9 insect cell system was attempted. The expression and localization in the plasma membrane of prestin in infected Sf9 cells were confirmed by Western blotting and immunofluorescence analysis, and prestin's functional activity was determined by patch-clamp measurements. Furthermore, to obtain prestin from the cells efficiently, culture conditions of the cells were examined, and it was clarified that cells should be harvested around 72 hours after infection. Quantitative Western blotting revealed that the maximal amount of prestin per liter of culture medium was around 800 μg. The results of this study indicate that the expression system which was constructed is potentially useful for purification of prestin due to the rapidity of its construction and its high yield.

【 授权许可】

Unknown