Mutually beneficial confluence of structure-based modeling of protein dynamics and machine learning methods

被引:12
作者
Banerjee, Anupam [1 ]
Saha, Satyaki [1 ]
Tvedt, Nathan C. [1 ,2 ]
Yang, Lee-Wei [3 ,4 ,5 ]
Bahar, Ivet [1 ]
机构
[1] Univ Pittsburgh, Computat & Syst Biol, Sch Med, Pittsburgh, PA 15261 USA
[2] Coll William & Mary, Computat & Appl Math & Stat, Williamsburg, VA 23185 USA
[3] Natl Tsing Hua Univ, Inst Bioinformat & Struct Biol, Hsinchu 300044, Taiwan
[4] Natl Tsing Hua Univ, PhD Program Biomed Artificial Intelligence, Hsinchu 300044, Taiwan
[5] Natl Ctr Theoret Sci, Phys Div, Taipei 106319, Taiwan
关键词
MOLECULAR-DYNAMICS; INTRINSIC DYNAMICS; SINGLE-PARAMETER; MUTATIONS; SITE; FLUCTUATIONS; INSIGHTS; DATABASE; SERVER; SPACE;
D O I
10.1016/j.sbi.2022.102517
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins sample an ensemble of conformers under physio-logical conditions, having access to a spectrum of modes of motions, also called intrinsic dynamics. These motions ensure the adaptation to various interactions in the cell, and largely assist in, if not determine, viable mechanisms of biological function. In recent years, machine learning frameworks have proven uniquely useful in structural biology, and recent studies further provide evidence to the utility and/or necessity of considering intrinsic dynamics for increasing their predictive ability. Efficient quantification of dynamics-based attributes by recently developed physics-based theories and models such as elastic network models provides a unique opportunity to generate data on dynamics for training ML models towards inferring mechanisms of protein function, assessing pathoge-nicity, or estimating binding affinities.
引用
收藏
页数:10
相关论文
共 75 条
  • [1] Adzhubei Ivan, 2013, Curr Protoc Hum Genet, VChapter 7, DOI 10.1002/0471142905.hg0720s76
  • [2] A method and server for predicting damaging missense mutations
    Adzhubei, Ivan A.
    Schmidt, Steffen
    Peshkin, Leonid
    Ramensky, Vasily E.
    Gerasimova, Anna
    Bork, Peer
    Kondrashov, Alexey S.
    Sunyaev, Shamil R.
    [J]. NATURE METHODS, 2010, 7 (04) : 248 - 249
  • [3] NMR spectroscopy captures the essential role of dynamics in regulating biomolecular function
    Alderson, T. Reid
    Kay, Lewis E.
    [J]. CELL, 2021, 184 (03) : 577 - 595
  • [4] Machine learning in protein structure prediction
    AlQuraishi, Mohammed
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2021, 65 : 1 - 8
  • [5] Anisotropy of fluctuation dynamics of proteins with an elastic network model
    Atilgan, AR
    Durell, SR
    Jernigan, RL
    Demirel, MC
    Keskin, O
    Bahar, I
    [J]. BIOPHYSICAL JOURNAL, 2001, 80 (01) : 505 - 515
  • [6] Perturbation-Response Scanning Reveals Ligand Entry-Exit Mechanisms of Ferric Binding Protein
    Atilgan, Canan
    Atilgan, Ali Rana
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2009, 5 (10)
  • [7] Direct evaluation of thermal fluctuations in proteins using a single-parameter harmonic potential
    Bahar, I
    Atilgan, AR
    Erman, B
    [J]. FOLDING & DESIGN, 1997, 2 (03): : 173 - 181
  • [8] The intrinsic dynamics of enzymes plays a dominant role in determining the structural changes induced upon inhibitor binding
    Bakan, Ahmet
    Bahar, Ivet
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (34) : 14349 - 14354
  • [9] Estimating Change in Foldability Due to Multipoint Deletions in Protein Structures
    Banerjee, Anupam
    Kumar, Amit
    Ghosh, Kushal Kanti
    Mitra, Pralay
    [J]. JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2020, 60 (12) : 6679 - 6690
  • [10] From systems to structure - using genetic data to model protein structures
    Braberg, Hannes
    Echeverria, Ignacia
    Kaake, Robyn M.
    Sali, Andrej
    Krogan, Nevan J.
    [J]. NATURE REVIEWS GENETICS, 2022, 23 (06) : 342 - 354