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Data-driven Multiscale Modeling of Signal Processing in Bacterial Chemotaxis

Research Project

Project/Area Number 16H04771
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Biophysics
Research InstitutionHokkaido University

Principal Investigator

李 振風  北海道大学, 電子科学研究所, 准教授 (90397795)

Project Period (FY) 2016-04-01 – 2017-03-31
Project Status Discontinued (Fiscal Year 2016)
Budget Amount *help
¥8,840,000 (Direct Cost: ¥6,800,000、Indirect Cost: ¥2,040,000)
Fiscal Year 2016: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
Keywords細胞情報・動態 / time series analysis / 生物物理
Outline of Annual Research Achievements

Change point analysis that does not require the knowledge of noise model has been developed to detect the time instants at which the observable value and the linear trend change in a time series. The model free change point detection has been applied to various single molecule time series, such as from single protein motor rotary measurements, gating current fluctuation in single ion channel patch clamp measurements, etc., to capture event switching that cannot be resolved using conventional thresholding and binning methods. The outcome from the change point analysis is the dwell time statistics of the system residing in various states, such as the pause and rotation states in rotary protein motor, sub-conductance states in ion channel gating, clockwise and counter-clockwise rotation modes in flagellar motor, different diffusive modes in bacterial chemotaxis, etc. As a next step of the project, the resulting dwell time statistics will then serve as the input to infer the underlying kinetic scheme of the system to reveal hidden kinetic states and transitions among the states.
On the other hand, the mathematical formalism of "transfer entropy" to quantify and detect information flow between multivariate time series has been generalized to detect "time dependent" flows. Before applying the new mathematical formalism to real bacterial chemotaxis time series, the theory is currently tested using time series generated from simple simulation models to benchmark its performance and validity.

Research Progress Status

28年度が最終年度であるため、記入しない。

Strategy for Future Research Activity

28年度が最終年度であるため、記入しない。

Report

(1 results)
  • 2016 Annual Research Report
  • Research Products

    (5 results)

All 2016

All Journal Article (3 results) (of which Int'l Joint Research: 3 results,  Peer Reviewed: 3 results,  Open Access: 2 results,  Acknowledgement Compliant: 1 results) Presentation (2 results) (of which Invited: 2 results)

  • [Journal Article] Extracting subcellular fibrillar alignment with error estimation: Application to microtubules2016

    • Author(s)
      Satoru Tsugawa, Nathan Hervieux, Oliver Hamant, Arezki Boudaoud, Richard S. Smith, Chun-Biu Li, Tamiki Komatsuzaki
    • Journal Title

      Biophysical Journal

      Volume: 110 Issue: 8 Pages: 1836-1844

    • DOI

      10.1016/j.bpj.2016.03.011

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Single molecule data analysis: An introduction2016

    • Author(s)
      M. Tavakoli, J.N. Taylor, C.B. Li, T. Komatsuzaki, S. Presse
    • Journal Title

      Adv. Chem. Phys.

      Volume: -

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Variable cell growth yields reproducible organ development through spatiotemporal averaging2016

    • Author(s)
      L. Hong, M. Dumond, S. Tsugawa, A. Sapala, A.-L. Routier-Kierzkowska, Y. Zhou, C. Chen, A. Kiss, M. Zhu, O. Hamant, R. S. Smith, T. Komatsuzaki, C.-B. Li, A. Boudaoud & A. H. K. Roeder
    • Journal Title

      Developmental Cell

      Volume: 38 Issue: 1 Pages: 15-32

    • DOI

      10.1016/j.devcel.2016.06.016

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] Single Molecule Time Series Analyses of F1-ATPase to Unveil the Roles of ATP Hydrolysis2016

    • Author(s)
      C.B. Li
    • Organizer
      Workshop on Super-functional Molecules
    • Place of Presentation
      Institute for Molecular Science, Okazaki, Japan
    • Year and Date
      2016-06-27
    • Related Report
      2016 Annual Research Report
    • Invited
  • [Presentation] A Nano-scale Key-and-Unlock Mechanism in the F1-ATPase revealed by Single Molecule Time Series Analysis2016

    • Author(s)
      C.B. Li
    • Organizer
      Beijing Computational Science Research Center
    • Place of Presentation
      Beijing Computational Science Research Center, China
    • Related Report
      2016 Annual Research Report
    • Invited

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Published: 2016-04-21   Modified: 2018-01-16  

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