Unsupervised Clustering of Subcellular Protein Expression Patterns in High-Throughput Microscopy Images Reveals Protein Complexes and Functional Relationships between Proteins

被引:27
|
作者
Handfield, Louis-Francois [1 ]
Chong, Yolanda T. [2 ]
Simmons, Jibril [3 ]
Andrews, Brenda J. [2 ]
Moses, Alan M. [1 ,3 ]
机构
[1] Univ Toronto, Dept Comp Sci, Toronto, ON M5S 1A1, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A1, Canada
[3] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON M5S 1A1, Canada
关键词
SACCHAROMYCES-CEREVISIAE; DYNAMIC PROTEOMICS; GLOBAL ANALYSIS; MITOTIC EXIT; YEAST; LOCALIZATION; PATHWAY; CLASSIFICATION; IDENTIFICATION; SEGMENTATION;
D O I
10.1371/journal.pcbi.1003085
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein subcellular localization has been systematically characterized in budding yeast using fluorescently tagged proteins. Based on the fluorescence microscopy images, subcellular localization of many proteins can be classified automatically using supervised machine learning approaches that have been trained to recognize predefined image classes based on statistical features. Here, we present an unsupervised analysis of protein expression patterns in a set of high-resolution, high-throughput microscope images. Our analysis is based on 7 biologically interpretable features which are evaluated on automatically identified cells, and whose cell-stage dependency is captured by a continuous model for cell growth. We show that it is possible to identify most previously identified localization patterns in a cluster analysis based on these features and that similarities between the inferred expression patterns contain more information about protein function than can be explained by a previous manual categorization of subcellular localization. Furthermore, the inferred cell-stage associated to each fluorescence measurement allows us to visualize large groups of proteins entering the bud at specific stages of bud growth. These correspond to proteins localized to organelles, revealing that the organelles must be entering the bud in a stereotypical order. We also identify and organize a smaller group of proteins that show subtle differences in the way they move around the bud during growth. Our results suggest that biologically interpretable features based on explicit models of cell morphology will yield unprecedented power for pattern discovery in high-resolution, high-throughput microscopy images.
引用
收藏
页数:19
相关论文
共 26 条
  • [1] An Unsupervised kNN Method to Systematically Detect Changes in Protein Localization in High-Throughput Microscopy Images
    Lu, Alex Xijie
    Moses, Alan M.
    PLOS ONE, 2016, 11 (07):
  • [2] Accurate Classification of Protein Subcellular Localization from High-Throughput Microscopy Images Using Deep Learning
    Parnamaa, Tanel
    Parts, Leopold
    G3-GENES GENOMES GENETICS, 2017, 7 (05): : 1385 - 1392
  • [3] High-throughput viral expression of cDNA-Green fluorescent protein fusions reveals novel subcellular addresses and identifies unique proteins that interact with plasmodesmata
    Escobara, NM
    Haupt, S
    Thow, G
    Boevink, P
    Chapmana, S
    Oparka, K
    PLANT CELL, 2003, 15 (07): : 1507 - 1523
  • [4] High-throughput protein expression of cDNA products as a tool in functional genomics
    Larsson, M
    Gräslund, S
    Li, YB
    Brundell, E
    Uhlén, M
    Höög, C
    Stähl, S
    JOURNAL OF BIOTECHNOLOGY, 2000, 80 (02) : 143 - 157
  • [5] Protein expression profiling arrays: tools for the multiplexed high-throughput analysis of proteins
    Jens R Sydor
    Steffen Nock
    Proteome Science, 1 (1)
  • [6] A high-throughput immobilized bead screen for stable proteins and multi-protein complexes
    Lockard, Meghan A.
    Listwan, Pawel
    Pedelacq, Jean-Denis
    Cabantous, Stephanie
    Nguyen, Hau B.
    Terwilliger, Thomas C.
    Waldo, Geoffrey S.
    PROTEIN ENGINEERING DESIGN & SELECTION, 2011, 24 (07): : 565 - 578
  • [7] High-Throughput Characterization of Viral and Cellular Protein Expression Patterns During JC Polyomavirus Infection
    Dushane, Jeanne K.
    Wilczek, Michael P.
    Crocker, Mason A.
    Maginnis, Melissa S.
    FRONTIERS IN MICROBIOLOGY, 2019, 10
  • [8] Recombinational cloning: A high-throughput gene transfer technology for functional analysis and protein expression.
    Hartley, J
    Brasch, M
    Temple, GF
    Cheo, D
    Polayes, D
    Harris, R
    Bebee, R
    Nelson, D
    Xu, W
    Dahmas, M
    Zuraitis, K
    Long, A
    Gerard, G
    Flynn, E
    Esposito, D
    Endress, G
    Rhodes, M
    Jessee, J
    MOLECULAR BIOLOGY OF THE CELL, 1999, 10 : 267A - 267A
  • [9] Annotation of novel proteins utilizing a functional genome shotgun coupled with high-throughput protein interaction mapping
    Malek, JA
    Wierzbowski, JM
    Dasch, GA
    Eremeva, ME
    McEwan, PJ
    McKernan, KJ
    COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2003, 68 : 331 - 334
  • [10] High-throughput competitive fluorescence polarization assay reveals functional redundancy in the S100 protein family
    Simon, Marton A.
    Ecsedi, Peter
    Kovacs, Gabor M.
    Poti, Adam L.
    Remenyi, Attila
    Kardos, Jozsef
    Gogl, Gergo
    Nyitray, Laszlo
    FEBS JOURNAL, 2020, 287 (13) : 2834 - 2846