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Transcript
[email protected]
AI for Synthetic Biology
@ IJCAI 2016
Aaron Adler
Fusun Yaman
ThisdocumentdoesnotcontaintechnologyorTechnicalDatacontrolledundereithertheU.S.
Interna9onalTrafficinArmsRegula9onsortheU.S.ExportAdministra9onRegula9ons.
1
Sponsors
[email protected]
2
Workshop Goals
[email protected]
•  Expose AI researchers to a new domain
•  Bring new tools and techniques to Synthetic
Biologists to help address hard problems
•  Cross pollenate the AI and SynBio communities
•  Develop collaborations between the
communities
•  Discuss next steps
3
Schedule
[email protected]
Time
Title
Authors
Affilia0ons
1:30
Welcome
A.Adler,F.Yaman
1:40
Introduc9ontoSynthe9cBiology
A.Adler,F.Yaman
BBN,USA
2:00
AIforSynthe9cBiology
F.Yaman,A.Adler
BBN,USA
2:25
Automatedreading,assemblyandexplana9onto
guidebiologicaldesign
N.Miskov-Zivanov
UniversityofPiTsburgh,
USA
2:50
DebuggingGene9cProgramswithBayesian
Networks
G.Karlebach,L.Woodruff,C.
VoigtandB.Gordon
MITBroadFoundry,USA
3:10
MolecularRobotsObeyingAsimov'sThreeLawsof
Robo9cs
G.Kaminka,R.Spokoini-Stern,Y.
Amir,N.AgmonandI.Bachelet
BarIlanUniversity&
Augmanity,Israel
3:30
CoffeeBreak
4:00
ACombinatorialDesignWorkflowforSearchand
Priori9za9oninLarge-ScaleSynthe9cBiology
ConstructAssembly J.Ng,A.Berliner,J.Lachoff,F.
Mazzoldi,E.Groban
AutodeskResearch,USA
4:20
MDP-basedPlanningforDesignofGene-Repression
ofCircuits
T.AmimeurandE.Klavins
UniversityofWashington,
USA
4:40
UsingMachineLearningtoInterpretUntargeted
MetabolomicsintheContextofBiologicalSamples
A.Tong,N.Alden,V.Porokhin,
N.Hassanpour,K.LeeandS.
Hassoun
TucsUniversity,USA
5:00
Discussionandclosingremarks
5:30
Workshopends
4
[email protected]
Introduction to Synthetic Biology
Aaron Adler
Fusun Yaman
ThisdocumentdoesnotcontaintechnologyorTechnicalDatacontrolledundereithertheU.S.
Interna9onalTrafficinArmsRegula9onsortheU.S.ExportAdministra9onRegula9ons.
Workpar9allysponsoredbyDARPAundercontractHR0011-10-C-0168.Theviewsandconclusions
containedinthisdocumentarethoseoftheauthorsandnotDARPAortheU.S.Government.
5
What is Synthetic Biology?
[email protected]
•  “… a maturing scientific discipline that combines
science and engineering in order to design and build
novel biological functions and systems” [SynBERC]
Program
CellsExecu9ng
Program
•  Synthetic biologists are working on diverse
applications:
–  New medical diagnostics and therapies
–  Extract harmful pollutants from the ground
–  Chemical production or detection
•  Synthetic Biology is at a crossroads: AI can help!
6
Synthetic Biology vs. Genetic Engineering
[email protected]
•  Genetic Engineering is the ability to read, copy,
and edit DNA so that controlled changes can be
made to organisms
•  Engineering is the application of scientific,
economic, social, and practical knowledge in
order to invent, design, build, maintain, and
improve structures, machines, devices, systems,
materials, and processes. (Wikipedia)
•  Understand the design enough to make a
prediction about how it will behave
7
Synthetic Biology as an Engineering
Discipline
[email protected]
•  Goal: Design sophisticated biological systems in a
reliable, efficient, and predictable manner
•  Useful engineering practices:
–  Libraries of “parts”, Component testing, Standards &
interfaces, Decoupling, Modularity, Computer aided design
•  Issues in engineering biological systems:
–  Device characterization, Impedance matching, Rules of
composition, Noise, Cellular context, Environmental
conditions, Rational design vs. directed evolution,
Persistence, Mutations, Crosstalk, Cell death, Chemical
diffusion, Motility, Incomplete models
•  A discipline that needs new engineering rule
–  The rules don’t have to be identical to natural evolution
[Weiss]
8
Why is this Important?
[email protected]
•  Breaking the complexity barrier:
DNA synthesis
1,080,000
583,000
1,000,000
Lengthinbasepairs
Circuit size
100,000
?
32,000
7,500
10,000
14,600
2,100 2,700
1,000
207
100
1975 1980 1985 1990 1995 2000 2005 2010
Year
•  Multiplication of research impact
•  Reduction of barriers to entry
[Purnick&Weiss,‘09]
9
*Samplingofsystemsinpublica9onswithexperimentalcircuits
More Recent Advances
[email protected]
[Weiss]
10
From Idea to Implementation
[email protected]
11
HierarchicalOrganiza9oninSynthe9cBiology
[email protected]
Applica0ons
Systemintegra0on
Modules
Gene0cparts
12
DNA, RNA, Proteins
[email protected]
•  DNA (Deoxyribonucleic acid)
is a double helix encoding
genetic instructions
–  Composed of nucleotides:
adenine (A), cytosine (C),
guanine (G), or thymine (T)
•  RNA (Ribonucleic acid) is
usually single stranded
–  Composed of nucleotides:
adenine (A), cytosine (C),
guanine (G), or uracil (U)
•  RNA can encode an amino
acid sequence that can in turn
[Wikimedia]
produce a protein
•  Expression dependent on cellular platform, e.g., animal,
yeast, bacteria, and cellular context, e.g., heart vs. skin cell
13
Common Machinery:
Transcriptional Logic
[email protected]
Timeconstantsoftheseprocessesare
ocenquiteslow,ac9ngontheorderof
minutes,hours,or(insomecases)days.
Transla)onisthedecodingoftheaminoacidsequence
ofanRNAsequencetoproduceaprotein,thereby
increasingtheconcentra9onofthatprotein.Proteinsare
Transcrip)onisthecopyingofaregionof
themain“machinery”ofacell.Amongotherthings,they
DNA,themoleculeinwhichgene9c
actassensors,asactuators,andasregulatorsofother
informa9onisencodedasasequenceof
Regula)onistheinterac9onofaproteinwiththepromoter
biologicalprocesses.
nucleo9des,intoastrandofRNA.
regionofaDNAsequence,therebymodula9ngtherateat
whichtranscrip9onactsontheregionofDNAcontrolledby
Degrada)onandDilu)onaretheprocessesbywhichtheconcentra9onof
thepromoter.Theproteinmayrepressthepromoter,
proteinsandRNAtranscriptsdecrease.Degrada9onisthechemicalbreakdown
inhibi9ngtranscrip9on,orismayac)vatethepromoter,
ofamoleculebycellularprocessesorbyitsowninstability.Dilu9onistheside
enhancingtranscrip9on.
effectofcellsgrowinganddividing:theeffec9veconcentra9onofanymolecule
14
dropspropor9onaltotheamountthatthevolumeofthecellincreases.
Focus on Information / Control
DNA
Chemical
RNApolymerase
4
Proteins
Structural
1
RNA
ribosome
promoter
Informa0onal
[email protected]
2
3
Degrada0on
&Dilu0on
Informa9onal:Representprocessesasdigitallogic,dataflows
Chemical:Cellularreac9onsarefundamentallyprobabilis9candchemical
Structural:Reac9onsdependonthephysicalstructureofDNA/RNA/Proteins/Cells
Most complex applications will require all three15
System Design
[email protected]
Environment
Cellularcontext
SENSORS
PROCESSING
temperature,
pH,light,
chemical
signals,
mechanical
force
ACTUATION
fluorescence,
movement,
electrical
ac9vity,
chemical
products
Synthe0ccircuit
• Number?
• Types?
• Sophis9ca9on?
§ Timing
§ States
• Number?
• Types?
§ Lookuptables
§ …
Highlevelgoal:developanengineeringdisciplineforbiology
16
Building Blocks
[email protected]
•  Features (Parts) are previously identified DNA
sequences that perform a specific biological
function
–  promoter initiates transcription
–  coding sequence for a protein Promoter
–  terminator that halts transcription
CDS
Terminator
•  Parts used as basis for engineering
•  Fluorescent proteins can be observed and used
to help understand what is going on in a cell
+
17
Genetic Regulatory Networks
[email protected]
•  A collection of DNA regions and their regulatory
interactions is called a genetic regulatory network (GRN)
–  Takes advantage of the modularity of the DNA molecule
–  Design of a desired computation
•  The GRN may be designed as a single DNA sequence or
as multiple separate sequences
–  Can operate as an insertion into the organism’s existing DNA, as
a virus, or as independent free-floating DNA loops (known as
plasmids)
IfthereisDox
ThenglowCyan
ElseglowYellow
Key
Dox
rtTA
pHef1a
Promoter
CFP
pTre
LacI
pTre
EYFP
pHef1a-
LacO1Oid
Protein
Repress
Ac9vate
18
Biological Circuits
[email protected]
•  Various forms of interaction can be used as
computational building blocks for building more
complex biological circuits
–  Deliberately analogous to electronic circuits
•  Loops in the regulatory network can be used for
feedback control or to create state memory
•  Allows an extremely wide variety of
computational and control systems to be
implemented as genetic regulatory networks
19
Digital Logic in an Analog World
[email protected]
ideal
(step fn)
reality
(sigmoidal)
Output Concentration
“1”
“0”
“0”
Input Concentration
“1”
•  Biological processes can support digital logic devices!
20
Genetic Building Block – Digital Inverter
[email protected]
0
1
input protein
(repressor)
output protein
Transcription /
Translation
P
CDS
21
Gene9cBuildingBlock–DigitalInverter
[email protected]
1
0
input protein
(repressor)
output protein
Transcription /
Translation
P
CDS
22
Interac9ngwithCells–IMPLIESGate
[email protected]
Repressor
Inducer
Output
input protein
(repressor)
Repressor
0
0
1
1
Inducer
0
1
0
1
Output
1
1
0
1
output protein
Transcription /
Translation
P
CDS
23
Interac9ngwithCells–IMPLIESGate
[email protected]
Repressor
Inducer
Output
inactive repressor
Repressor
0
0
1
1
Inducer
0
1
0
1
Output
1
1
0
1
output protein
Transcription /
Translation
P
CDS
24
Abstract Genetic Regulatory Network (A-GRN) [email protected]
Kz Hz Dz αz γz
Z
Kx Hx Dx αx γx
Ky Hy Dy αy γy
Y
X
•  Defines logical relationship between abstract parts
•  The GRN above
–  Y induces and Z represses the transcription of X
•  The overall behavior depends on chemical properties
–  degradation (γ ), dissociation (D), fold activation (K), basal
expression (α), cooperativity (H)
25
Simulating System Behavior
[email protected]
( Kz , Hz , Dz )
(αx , γx )
( Ky , Hy , Dy )
•  Change in concentration of the chemicals approximated
using differential equations
•  The input/output relationship between X&Y and X&Z
X
Y
Z
26
DNA Assembly Techniques
• 
• 
• 
• 
• 
[email protected]
BioBricks
Magnetic Beads
Gateway-Gibson
Golden Gate
Enzymes break DNA
apart allowing parts
to join together
[igem.org]
27
Getting the New DNA into Cells
[email protected]
•  How do you get new DNA into the cell?
–  Transfection
•  Chemical and non-chemical methods
–  Lipofection
–  Virus delivery
•  DNA can be:
–  chromosomally integrated OR
–  transiently transfected OR
–  on a separate plasmid
•  How do you measure the results?
– 
– 
– 
– 
– 
fluorescence
mass spectrometry
anti-body assays
cells emit other chemicals
RNA/DNA assays, …
28
Simple Circuit Example
[email protected]
“Fluoresce green when doxycycline is present”
Dox
rtTA
GFP
Currently, even something this simple isn’t easy…
29
Sense/Actuate Example
[email protected]
Ara
AraC
pBAD
GFP
NoArabinose
pBAD
TetR
pTet
RFP
HighDoseArabinose
30
Synthetic Biology
[Levskaya]
[Medford]
[email protected]
[Weiss]
[Hasty]
31
OutlookforApplica9ons
[email protected]
Bioenergyproduc0on
• biodiesel
• hydrogen
• methane
• …
Microbialbiochemical
synthesis
• artemisinin
• otherpharmaceu9cals
Environmentalapplica0ons
• environmentalremedia9on
• toxinsensing
• explosivesensing
Biomedicalapplica0ons
• cancertherapeu9cagents
• ar9ficial9ssuehomeostasis
• programmed9ssueregenera9on
• ar9ficialimmunesystem
32
Example genetic circuit applications
Fermentation control
[email protected]
CAR T-cell Therapy
33