DocumentCode
2421169
Title
Control of biological clock activity capsulated by lipid-mono-layer
Author
Kojima, Masaru ; Nakajima, Masahiro ; Takiguchi, Kingo ; Homma, Michio ; Kondo, Takao ; Fukuda, Toshio
Author_Institution
Dept. of Micro-Nano Syst. Eng., Nagoya Univ., Nagoya, Japan
fYear
2012
fDate
14-18 May 2012
Firstpage
2196
Lastpage
2201
Abstract
In this paper, we try to establish new technique that the components of the biological clock are reconstituted into the liposome. In other words, we try to produce a nano size clock, capsulated into the liposome, made by protein molecules. The circadian clock is a basic cellular system found in almost all organisms. This clock generates self-sustained oscillations under constant conditions with a ≈ 24-hour (circadian) period. In cyanobacteria, circadian clock could be reconstituted in vitro only by mixing the three clock proteins, KaiA, KaiB, KaiC, with adenosine triphosphate (ATP). So we reconstitute these proteins and adenosine triphosphate (ATP) into phospholipid-coated microdroplet and confirmed the clock function. The clocks in phospholipids-coated microdroplet indicate long period more than 24 hours. In this case, period length became 35 hour, self-sustaining oscillation was reaming with little dumping. To reveal why the time cycle became long period, we observed localization of Kai proteins in phospholipid-coated microdroplets by using fluorescents labeled Kai proteins under fluorescent (confocal) microscopy. From the observation of localization of Kai proteins, we found KaiB protein was distributed equivalently, on the other hand, KaiC protein was located near membrane of phospholipid-coated microdroplet. These results indicate that different localization between Kai proteins cause long period oscillation and we could control period length depend on calculation data from localization.
Keywords
biocomputing; cellular biophysics; circadian rhythms; lipid bilayers; molecular biophysics; proteins; robots; KaiB protein; KaiC protein; adenosine triphosphate; basic cellular system; biological clock activity control; circadian clock; clock proteins; cyanobacteria; fluorescent microscopy; fluorescents labeled Kai proteins; lipid-mono-layer; liposome; nano size clock; phospholipid-coated microdroplet; protein molecules; self-sustained oscillations; Biomembranes; Chronobiology; Clocks; Fluorescence; Microscopy; Oscillators; Proteins;
fLanguage
English
Publisher
ieee
Conference_Titel
Robotics and Automation (ICRA), 2012 IEEE International Conference on
Conference_Location
Saint Paul, MN
ISSN
1050-4729
Print_ISBN
978-1-4673-1403-9
Electronic_ISBN
1050-4729
Type
conf
DOI
10.1109/ICRA.2012.6225353
Filename
6225353
Link To Document