Thresholding of cryo-EM density maps by false discovery rate control

被引:29
作者
Beckers, Maximilian [1 ,2 ,6 ,7 ]
Jakobi, Arjen J. [1 ,3 ,4 ,8 ]
Sachse, Carsten [1 ,5 ]
机构
[1] European Mol Biol Lab EMBL, Struct & Computat Biol Unit, Meyerhofstr 1, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab EMBL, Fac Biosci, Meyerhofstr 1, D-69117 Heidelberg, Germany
[3] DESY, Hamburg Unit, Notkestr 85, D-22607 Hamburg, Germany
[4] Hamburg Ctr Ultrafast Imaging CUI, Luruper Chaussee 149, D-22761 Hamburg, Germany
[5] Forschungszentrum Julich, Ernst Ruska Ctr Microscopy & Spect Elect ER C 3 S, D-52425 Julich, Germany
[6] EMBL, Heidelberg, Germany
[7] Heidelberg Univ, Heidelberg, Germany
[8] Delft Univ Technol, Dept Bionanosci, Kavli Inst Nanosci, Maasweg 9, NL-2629 HZ Delft, Netherlands
来源
IUCRJ | 2019年 / 6卷
关键词
electron cryo-microscopy; signal detection; false discovery rate; cryo-EM density; subtomogram averaging; local resolution; ligand binding; TOBACCO-MOSAIC-VIRUS; ELECTRON-MICROSCOPY; BETA-GALACTOSIDASE; ATOMIC MODEL; RESOLUTION; RECONSTRUCTION; SYSTEM;
D O I
10.1107/S2052252518014434
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cryo-EM now commonly generates close-to-atomic resolution as well as intermediate resolution maps from macromolecules observed in isolation and in situ. Interpreting these maps remains a challenging task owing to poor signal in the highest resolution shells and the necessity to select a threshold for density analysis. In order to facilitate this process, a statistical framework for the generation of confidence maps by multiple hypothesis testing and false discovery rate (FDR) control has been developed. In this way, three-dimensional confidence maps contain signal separated from background noise in the form of local detection rates of EM density values. It is demonstrated that confidence maps and FDR-based thresholding can be used for the interpretation of near-atomic resolution single-particle structures as well as lower resolution maps determined by subtomogram averaging. Confidence maps represent a conservative way of interpreting molecular structures owing to minimized noise. At the same time they provide a detection error with respect to background noise, which is associated with the density and is particularly beneficial for the interpretation of weaker cryo-EM densities in cases of conformational flexibility and lower occupancy of bound molecules and ions in the structure.
引用
收藏
页码:18 / 33
页数:16
相关论文
共 62 条
  • [1] PHENIX: a comprehensive Python']Python-based system for macromolecular structure solution
    Adams, Paul D.
    Afonine, Pavel V.
    Bunkoczi, Gabor
    Chen, Vincent B.
    Davis, Ian W.
    Echols, Nathaniel
    Headd, Jeffrey J.
    Hung, Li-Wei
    Kapral, Gary J.
    Grosse-Kunstleve, Ralf W.
    McCoy, Airlie J.
    Moriarty, Nigel W.
    Oeffner, Robert
    Read, Randy J.
    Richardson, David C.
    Richardson, Jane S.
    Terwilliger, Thomas C.
    Zwart, Peter H.
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2010, 66 : 213 - 221
  • [2] Atomic model of the F420-reducing [NiFe] hydrogenase by electron cryo-microscopy using a direct electron detector
    Allegretti, Matteo
    Mills, Deryck J.
    McMullan, Greg
    Kuehlbrandt, Werner
    Vonck, Janet
    [J]. ELIFE, 2014, 3
  • [3] A TEST OF GOODNESS OF FIT
    ANDERSON, TW
    DARLING, DA
    [J]. JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1954, 49 (268) : 765 - 769
  • [4] Appen A. von, 2015, NATURE, V526, P140
  • [5] An atomic structure of human γ-secretase
    Bai, Xiao-chen
    Yan, Chuangye
    Yang, Guanghui
    Lu, Peilong
    Ma, Dan
    Sun, Linfeng
    Zhou, Rui
    Scheres, Sjors H. W.
    Shi, Yigong
    [J]. NATURE, 2015, 525 (7568) : 212 - +
  • [6] Ribosome structures to near-atomic resolution from thirty thousand cryo-EM particles
    Bai, Xiao-chen
    Fernandez, Israel S.
    McMullan, Greg
    Scheres, Sjors H. W.
    [J]. ELIFE, 2013, 2
  • [7] Atomic Resolution Cryo-EM Structure of β-Galactosidase
    Bartesaghi, Alberto
    Aguerrebere, Cecilia
    Falconieri, Veronica
    Banerjee, Soojay
    Earl, Lesley A.
    Zhu, Xing
    Grigorieff, Nikolaus
    Milne, Jacqueline L. S.
    Sapiro, Guillermo
    Wu, Xiongwu
    Subramaniam, Sriram
    [J]. STRUCTURE, 2018, 26 (06) : 848 - +
  • [8] 2.2 Å resolution cryo-EM structure of β-galactosidase in complex with a cell-permeant inhibitor
    Bartesaghi, Alberto
    Merk, Alan
    Banerjee, Soojay
    Matthies, Doreen
    Wu, Xiongwu
    Milne, Jacqueline L. S.
    Subramaniam, Sriram
    [J]. SCIENCE, 2015, 348 (6239) : 1147 - 1151
  • [9] Structure of β-galactosidase at 3.2-Å resolution obtained by cryo-electron microscopy
    Bartesaghi, Alberto
    Matthies, Doreen
    Banerjee, Soojay
    Merk, Alan
    Subramaniam, Sriram
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (32) : 11709 - 11714
  • [10] Benjamini Y, 2001, ANN STAT, V29, P1165