Computational Tool for Ensemble Averaging of Single-Molecule Data

被引:6
作者
Blackwell, Thomas [1 ]
Stump, W. Tom [1 ]
Clippinger, Sarah R. [1 ]
Greenberg, Michael J. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
MYOSIN-I; MUSCLE; STROKE; FORCES; MOTOR; POWER;
D O I
10.1016/j.bpj.2020.10.047
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Molecular motors couple chemical transitions to conformational changes that perform mechanical work in a wide variety of biological processes. Disruption of this coupling can lead to diseases, and therefore there is a need to accurately measure mechanochemical coupling in motors in both health and disease. Optical tweezers with nanometer spatial and millisecond temporal resolution have provided valuable insights into these processes. However, fluctuations due to Brownian motion can make it difficult to precisely resolve these conformational changes. One powerful analysis technique that has improved our ability to accurately measure mechanochemical coupling in motor proteins is ensemble averaging of individual trajectories. Here, we present a user-friendly computational tool, Software for Precise Analysis of Single Molecules (SPASM), for generating ensemble averages of single-molecule data. This tool utilizes several conceptual advances, including optimized procedures for identifying single-molecule interactions and the implementation of a change-point algorithm, to more precisely resolve molecular transitions. Using both simulated and experimental data, we demonstrate that these advances allow for accurate determination of the mechanics and kinetics of the myosin working stroke with a smaller set of data. Importantly, we provide our open-source MATLAB-based program with a graphical user interface that enables others to readily apply these advances to the analysis of their own data.
引用
收藏
页码:10 / 20
页数:11
相关论文
共 28 条
  • [1] Computational Tool to Study Perturbations in Muscle Regulation and Its Application to Heart Disease
    Barrick, Samantha K.
    Clippinger, Sarah R.
    Greenberg, Lina
    Greenberg, Michael J.
    [J]. BIOPHYSICAL JOURNAL, 2019, 116 (12) : 2246 - 2252
  • [2] Beausang JF, 2011, METHOD ENZYMOL, P431, DOI [10.1016/S0076-6879(11)87015-1, 10.1016/B978-0-12-381270-4.00015-9]
  • [3] Two independent mechanical events in the interaction cycle of skeletal muscle myosin with actin
    Capitanio, M
    Canepari, M
    Cacciafesta, P
    Lombardi, V
    Cicchi, R
    Maffei, M
    Pavone, FS
    Bottinelli, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (01) : 87 - 92
  • [4] Capitanio M, 2012, NAT METHODS, V9, P1013, DOI [10.1038/NMETH.2152, 10.1038/nmeth.2152]
  • [5] Kinetic Schemes for Post-Synchronized Single Molecule Dynamics
    Chen, Chunlai
    Greenberg, Michael J.
    Laakso, Joseph M.
    Ostap, E. Michael
    Goldman, Yale E.
    Shuman, Henry
    [J]. BIOPHYSICAL JOURNAL, 2012, 102 (06) : L23 - L25
  • [6] Disrupted mechanobiology links the molecular and cellular phenotypes in familial dilated cardiomyopathy
    Clippinger, Sarah R.
    Cloonan, Paige E.
    Greenberg, Lina
    Ernst, Melanie
    Stump, W. Tom
    Greenberg, Michael J.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (36) : 17831 - 17840
  • [7] Identification of functional differences between recombinant human α and β cardiac myosin motors
    Deacon, John C.
    Bloemink, Marieke J.
    Rezavandi, Heresh
    Geeves, Michael A.
    Leinwand, Leslie A.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2012, 69 (13) : 2261 - 2277
  • [8] SINGLE MYOSIN MOLECULE MECHANICS - PICONEWTON FORCES AND NANOMETER STEPS
    FINER, JT
    SIMMONS, RM
    SPUDICH, JA
    [J]. NATURE, 1994, 368 (6467) : 113 - 119
  • [9] Goldman Y. E., 2012, COMPREHENSIVE BIOPHY, P1
  • [10] Greenberg MJ, 2017, METHODS MOL BIOL, V1486, P483, DOI 10.1007/978-1-4939-6421-5_19