metabolomics,pathway,analysis, - abrf association of ... · metabolic,network, •...
TRANSCRIPT
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Metabolomics Pathway analysis
Anatoly Sorokin
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Metabolomics
• Metabolomics is the "systema7c study of the unique chemical fingerprints that specific cellular processes leave behind", the study of their small-‐molecule metabolite profiles. Daviss, BenneE (2005) The Scien7st 19 (8): 25–28
• Younger sister?: de Réaumur, RAF (1752). "Observa7ons sur la diges7on des oiseaux". Histoire de l'academie royale des sciences 1752: 266, 461.
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Metabolic network
• Pathway is a series of reac7ons conver7ng set of substrate into set of products
• Pathway defini7on is subjec7ve and non-‐standard
• Pathways are overlapping • Easier to talk about whole network
– FBA – Extreme pathway etc
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Network representa7ons
Stoichiometry matrix Connec7vity matrix
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Matrix to the network
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Currency metabolites
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With or without currency metabolites
Metabolic network of S. pneumonia (616 reac7ons)
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Network metrics for metabolic network
• A typical genome scale metabolic network contains one thousand reac7ons/metabolites.
• We need to characterize importance of nodes and edges in the network
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Neighbours and degree
r1 r5
r4
r2
r3
Neighbours: directly linked nodes
K-‐neighbours: nodes linked with a node in k steps.
Degree: the number of links to its neighbours from a node (may not equal to the number of neighbours).
For directed network: input and output degree.
For r2, neighbours are 2, 2-‐neighbours are 4
Degree is 2, input degree is 2 and output degree is 1.
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Connec7on degree distribu7on
P(k): Percentage of nodes with a degree k or not less than k (Cumulative distribution).
Power law degree distribution indicates a scale free network: A few nodes (hubs) have very high degree while most nodes have very low degree.
How node degrees distributed in a network.
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Random network and scale free network
Many real networks are scale free networks.
Robust on random failure but vulnerable under aimed aEack at the highly connected nodes (hubs). Scale free feature is the result of evolu7on (rich get richer genera7ve model, like web)
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Hub metabolites
Glycerate-3-phosphate, D-Ribose-5-phosphate, Acetyl-CoA, Pyruvate, D-Xylulose 5-phosphate D-Fructose 6-phosphate, 5-Phospho-D-ribose 1-diphosphate, L-Glutamate, D-Glyceraldehyde 3-phosphate, L-Aspartate, Propanoyl-CoA, Malonyl-ACP, Succinate, Acetate, Isocitrate, Fumarate
E. Coli metabolic network
Most hubs are in central pathways. However, if currency metabolites are included in the network, Most hubs would be currency metabolites
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Node Centrality
Closeness centrality of node x:
d(x,y) the path length between node x and node y
U the set of all nodes
average path length between x and the other nodes
The central nodes have short path lengths to other nodes in the network
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The most central metabolites in the metabolic network of E. coli
Metabolite Centrality Pyruvate 0.225
Actyl-CoA 0.210
Malate 0.204
2KD6PG 0.203
Acetate 0.201
Acetaldehyde 0.199
G3P 0.198
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Betweenness Centrality • the frac7on of shortest paths between pairs of nodes that passes through a given node.
A
C B
The most effec7ve target to break down the network (Robustness of network)
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Network Global Connec7vity
Degree distribution tells nothing about global connectivity
The right network can have short average path length though not connected at all
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Strongly or weakly connected components a connected component is a maximal connected subgraph. Two nodes are defined to be in the same connected component if there exists a path between them. If link direc7on is considered it is strongly connected, otherwise weakly connected.
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SC distribu7on in a metabolic network
Num
ber
GSC: Giant strong component
One big SC and many small SCs
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Connectivity structure of MN
Giant strong component (GSC)
metabolites fully converted and
conver7ble to each other
Substrate subset (93) converted to metabolite in GSC
Product subset (161) produced from metabolites in GSC
274 out of total 811 metabolites
Isolated subset (283)
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Bow-tie: a general structure of biological and physical networks
Giant Strong Component
disconnected components
OUT subset
IN subset
• Metabolic network • Signal transduc7on • Web pages network • Material processing and other tech. systems
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Tools for network analysis
• KNEVA hEp://csb.inf.ed.ac.uk/kneva • Pajek (good manual and book): hEp://pajek.imfm.si/doku.php
• Cytoscape hEp://www.cytoscape.org/ (for Biological networks, mapping data), many plugins
• Bioconductor and R (SNA) • Java and Python packages (NetworkX)
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Network databases
• KEGG • Metacyc • Yeast (hEp://www.comp-‐sys-‐bio.org/yeastnet/)
• Human-‐specific networks – Recon1 (Palsson group, 1496 ORFs, 2004 proteins, 2766 metabolites and 3311 reac7ons)
– EHMN (Edinburgh group, 2671 compounds, 2322 genes, 2823 reac7ons 66 pathways)
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Metabolomics
• Chemometric – Spectral method based – Compounds are not defined
– Feature extrac7on – Qualita7ve
• Quan7ta7ve – MS method based – Compounds are defined
– Quan7ta7ve
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Pathway analysis in metabolomics
• Quan7ta7ve metabolomics data is similar to microarray data
• Can be processed and understood in similar way
• MetaboAnalyst (www.metaboanalyst.ca) on-‐line tool for data analysis in metabolomics
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MetaboAnalyst
Nucleic Acids Research, 2009, Vol. 37
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Pathway analysis in metabolomics
• We have data in “standard” format similar to transcriptomics and proteomics
• We have networks and pathways
• We can apply standard pathway analysis – Pure metabolomics – Metabolomics/transcriptomics
• MetPA (hEp://metpa.metabolomics.ca) online tool for metabolic pathway analysis
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Compound mapping
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Pathway impact
• Calculate importance of metabolites, found in the pathway – Degree – Betweenness
PI =
�found
Impi�all
Impi
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Pathway Impact
• P is calculated from GSE analysis
• Most significant pathways has low impact
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Metabolome/Transcriptome
• Pa7l and Nielsen 2005 • Convert metabolic network into compound-‐enzyme
Glucose
Glucose-6-phosphate
Hexokinase
ATP
ADP
cytosol
Glucose
Glucose-6-phosphate
Hexokinase
ATP
ADP
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Iden7fy reporter metabolite
• Calculate Z-‐score for each enzyme
• Calculate Z-‐score for metabolite
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Tools and database
• Experiment repository: www.metabolome-‐express.org
• Metscape2 metscape.ncibi.org
• Vanted vanted.ipk-‐gatersleben.de/ • MetPA metpa.metabolomics.ca/
• MetaboAnalyst
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SBGN
• To analyse • To discuss • To share
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Can a Biologist Understand This Diagram?
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From Holmes WF et al. (2003) Early events in the induction of apoptosis in ovarian carcinoma cells by CD437: activation of the p38 MAP kinase signal pathway. Oncogene 22: 6377–6386.
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Can a Biologist Understand This Diagram?
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Do these arrows have the same meaning?
From Holmes WF et al. (2003) Early events in the induction of apoptosis in ovarian carcinoma cells by CD437: activation of the p38 MAP kinase signal pathway. Oncogene 22: 6377–6386.
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Can a Biologist Understand This Diagram?
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Do these arrows have the same meaning? Are these
different types of entity?
What is this?
From Holmes WF et al. (2003) Early events in the induction of apoptosis in ovarian carcinoma cells by CD437: activation of the p38 MAP kinase signal pathway. Oncogene 22: 6377–6386.
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Can a Biologist Understand This Diagram?
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Do these arrows have the same meaning? Are these
different types of entity?
What is this?
How about these?
From Holmes WF et al. (2003) Early events in the induction of apoptosis in ovarian carcinoma cells by CD437: activation of the p38 MAP kinase signal pathway. Oncogene 22: 6377–6386.
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What Happens if one Cannot Read the Blueprint
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Process Descrip7on
maps
En7ty Rela7onship
maps
Ac7vity Flow
maps
Unambiguous
Mechanis7c
Sequen7al Combinatorial
explosion
Unambiguous
Mechanis7c
Non-‐Sequen7al
Ambiguous
Conceptual Sequen7al
Graph Trinity: Three Languages in One
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Three Orthogonal Projec7ons of Biology
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SBGN Process Descrip7on Language
• Inspired and based on Kitano’s Process Diagram Nota7on • A Process Descrip7on (PD) Diagram represents all molecular
processes and interac7ons occurring between various biochemical en77es
• It depicts how en77es transi7on forms as a result of biochemical reac7ons (including non-‐covalent modifica7ons such as binding)
• Most of the classic metabolic pathways (e.g., glycolysis and TCA cycle) in biochemistry textbooks were drawn in this approach
• Though not the conven7onal approach for drawing signaling pathways, this approach captures the details of biochemical reac7ons within the pathway network and provides, in most cases, unambiguous interpreta7on of pathway mechanisms
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En7ty Types
LABEL LABEL LABEL LABEL
Unspecified entity
Simple chemical
Macromolecule Nucleic acid feature
Macromolecules: biochemical substances that are built up from the covalent linking of pseudo-‐iden7cal units. Examples of macromolecules include proteins, nucleic acids (RNA, DNA), and polysaccharides (glycogen, cellulose, starch, etc.).
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Macromolecular Pools: State Variables
• Pool is set of molecules somehow undis7nguishable
• Molecules can be in different state – (Non)phosphorylated – Open/close channel – Modified at some state
R R P R
Ch
Close
Ch
Open
Kinase
P@237
2P
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Complex and Mul7mer • Represents complexes of molecules held together by non-‐covalent bonds
• Mul7mer require cardinality
• Can have state variables – In mul7mer it means that all monomers have same state
– Use complex if not the same states
N:2
LABEL
N:2
LABEL LABEL
N:2 LABEL
LABEL
Multimers
Complex
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Key Concept: Process
• Process: conversion of element of one pool to another
• Special cases: – Non-‐covalent binding
• Associa7on • Dissocia7on
– Incompleteness • Uncertain process • OmiEed process
?
//
Association
Dissociation
Process
Uncertain process
Omitted process
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Arcs
• Using pools by process – Consump7on/produc7on – Stoichiometry (op7onal)
• Regula7ng process rate – S7mula7on – Inhibi7on – Catalysis
• Requirement for process – Necessary s7mula7on
production
catalysis
stimulation
inhibition
necessary stimulation
modulation
consumption 2
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Compartments
• Container to represent physical or logical structure – Free form – Visually thicker line
• The same en7ty pools in different compartments are different
• Compartments are independent • Overlapping do not mean containment
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49 Neuro-‐muscular Junc7on
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Ac7vity Flow: Abstrac7on
• Main concept is Biological Ac7vity – Each node represents an ac7vity, but not the en7ty
– Mul7ple nodes can be used to represent ac7vi7es from one en7ty (e.g., receptor protein kinase)
– One node can be used to represent ac7vi7es from a group of en77es (e.g., a complex, generics etc.)
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Material and Conceptual Types in AF
• Ac7vity node is rectangular to emphasize similarity to reac7on
• Unit of informa7on has shape according to node type
• Unit of informa7on can carry name of en7ty, which has the ac7vity
Activity
mt:ion
LABEL LABEL
Perturbation Phenotype
Activity
mt:prot
Activity of ion Activity of protein
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Regulatory Arcs
• Operates on ac7vi7es • Shows influences
– Posi7ve • Catalysis • S7mula7on
– Nega7ve • Inhibi7on
– Required • Necessary s7mula7on
Positive influence
Negative influence
Necessary stimulation
Unknown influence
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Logical Gates
• Three main logic opera7ons – AND: all are required – OR: any combina7on is required – NOT: prevent influence
• Crucial for AF – No complex – No outcome – No modifica7ons
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Ac7vity Flow Map is Ambiguous
• AF diagrams are ambiguous
• An AF diagram should be associated with either a PD or ER diagram, if possible
• Automa7c conversion between PD and/or ER to AF is planed
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Example HRG HER3
mt:prot
HER2
mt:prot
Shc
mt:prot PI3K
mt:prot
GS
Ras
Raf
MEK
ERK
PP2A
PTEN PIP3
Akt
PDK
Apoptosis
2C4