Week 2a PDF
Week 2a PDF
Week 2a PDF
!
Philip!E.!Bourne!([email protected])
It%Was%the%Best%of%Times,%It%Was%the%
Worst%of%Times%
SPPS273 1/10/13%
2%
OMICS%D%The%Best%of%
Times%
SPPS273 1/10/13%
3%
The%Worst%of%Times%
Source: http://www.pharmafocusasia.com/strategy/drug_discovery_india_force_to_reckon.htm
SPPS273 1/10/13%
4%
Stated%Another%%
Let%OpKmism%Rule%
Way%
• Glass ½ Empty: drug • Let optimism rule – let
discovery in the IT, traditional
traditional sense is in a computational
woeful state chemistry and
• Glass ½ Full: cheminfomatics meet
– We have an explosion of bioinformatics, systems
data and hence a new biology and information
emerging understanding science to discover
of complex biological drugs in new ways –
systems Systems Pharmacology
– Information technology is
advancing rapidly
SPPS273 1/10/13%
5%
The$Take$Home$Message$
Agenda%
SPPS273 1/10/13%
6%
My%PerspecKve/Bias%
• We work in the area of structural
bioinformatics & more broadly
computational biology
• We distribute the equivalent to ¼
the Library of Congress to approx.
300,000 scientists each month
• We are interested in improving the
drug discovery process through
computationally driven hypotheses
on the complete biological system
– systems pharmacology
• Personally:
– Open science advocate
– Started 4 companies
– Spent whole life in the ivory tower
– AVC of Innovation & Industrial
Alliances
SPPS273 1/10/13%
7%
My$Perspec2ve/Bias$
The Omics Driver
• DNA sequence data
are doubling every 5
months
• Funders are
demanding data
sharing plans
• The long tail is
neglected
Year"
SPPS273 1/10/13%
9%
The$Omics$Revolu2on$ Courtesy%of%the%RCSB%Protein%Data%Bank%
The OMICS Revolution in One Slide
Metagenomics%
• New%type%of%genomics%
• New%data%(and%lots%of%it)%
and%new%types%of%data%–%
IniKal%ocean%survey%
– 17M%new%(predicted%
proteins!)%4D5%x%growth%
in%just%few%months%and%
much%more%coming%
– New%challenges%and%
exacerbaKon%of%old%
challenges%
SPPS273 1/10/13%
11%
The$Omics$Revolu2on$
Metagenomics:%Early%Results%
• More%then%99.5%%of%DNA%in% • Everything%we%touch%
very%environment%studied% turns%out%to%be%a%gold%
represent%unknown% mine%
organisms% • Environments%studied:%
– Culturable%organisms%are%
– Water%(ocean,%lakes)%
excepKons,%not%the%rule%
– Soil%
• Most%genes%represent%
– Human%body%(gut,%oral%
distant%homologs%of%known% cavity,%human%
genes,%but%there%are% microbiome)%
thousands%of%new%families%
SPPS273 1/10/13%
12%
The$Omics$Revolu2on$
Metagenomics%New%Discoveries%
Environmental%(red)%vs.%Currently%Known%PTPases%(blue)%
1
SPPS273 1/10/13%
13%
The$Omics$Revolu2on$
Warning:%
With%Explosive%Growth%Comes%
Problems:%
%
Currently%30%%of%FuncKonal%
AnnotaKons%in%Databases%May%be%
Wrong%
SPPS273 1/10/13%
14%
The$Omics$Revolu2on$
Agenda%
SPPS273 1/10/13%
15%
Towards%Open%Science%
• Open%access%publishing%
• Open%source%socware%
• GeneraKon%of%scienKsts%weaned%on%social%networks%
• Blogs,%wikis,%social%bookmarking%etc.%are%becoming%a%
valid%form%of%scienKfic%discourse%%
hep://www.osdd.net/%
SPPS273 1/10/13%
16%
Open$Science$
An%Exemplar%of%Open%Science%
www.sagebase.org%
SPPS273 1/10/13%
17%
Open$Science$
The%Open%Access%Baele%is%Not%Won,%
but%its%Looking%Good%
SPPS273 1/10/13%
18%
Open$Science$
Agenda%
SPPS273 1/10/13%
19%
Why Don’t we Do Better?
A Couple of Observations
• Gene%knockouts%only%effect%phenotype%in%10D20%%
of%cases%,%why?%%
– redundant%funcKons%%
– alternaKve%network%routes%%
– robustness%of%interacKon%networks%
A.L.$Hopkins$Nat.$Chem.$Biol.$2008$4:682I690$
• 35%%of%biologically%acKve%compounds%bind%to%
more%than%one%target% Paolini$et$al.$Nat.$Biotechnol.$2006$24:805–815$
SPPS273 1/10/13%
20%
Drug$Discovery$–$Some$Inconveneint$Truths$
Why Don’t we Do Better?
A Couple of Observations
• Tykerb – Breast cancer
• Gleevac – Leukemia, GI
cancers
• Nexavar – Kidney and liver
cancer
• Staurosporine – natural product
– alkaloid – uses many e.g.,
antifungal antihypertensive
Collins%and%Workman%2006%Nature$Chemical$Biology$2%689D700%
SPPS273 1/10/13%
21%
Drug$Discovery$–$Some$Inconvenient$Truths$
ImplicaKons%
• Ehrlich s%philosophy%of%magic%bullets%targeKng%
individual%chemoreceptors%has%not%been%realized%
• Stated%another%way%–%The%noKon%of%one%drug,%one%
target,%one%disease%is%a%liele%naïve%in%a%complex%
system%
SPPS273 1/10/13%
22%
Drug$Discovery$–$Some$Inconvenient$Truths$
Agenda%
SPPS273 1/10/13%
23%
What%if…%
• We%can%characterize%a%proteinDligand%
binding%site%from%a%3D%structure%
(primary%site)%and%search%for%that%site%
on%a%proteome%wide%scale?%
• We%could%perhaps%find%alternaKve%
binding%sites%(offDtargets)%for%exisKng%
pharmaceuKcals%and%NCEs?%
SPPS273 1/10/13%
24%
Systems$Pharmacology$–$Example$from$Our$Lab$
What%Do%These%OffDtargets%Tell%Us?%
• PotenKally%many%things:%
1. Nothing%
2. How%to%opKmize%a%NCE%
3. A%possible%explanaKon%for%a%sideDeffect%of%a%drug%
already%on%the%market%
4. A%possible%reposiKoning%of%a%drug%to%treat%a%
completely%different%condiKon%
5. The%reason%a%drug%failed%%
6. A%mulKDtarget%strategy%to%aeack%a%pathogen%
%
SPPS273 1/10/13%
25%
Systems$Pharmacology$–$Example$from$Our$Lab$
Need%to%Start%with%a%3D%DrugDReceptor%Complex%
D%The%PDB%Contains%Many%Examples%
Generic Name Other Name Treatment PDBid
26
Systems$Pharmacology$–$Example$from$Our$Lab$
A!Reverse!Engineering!Approach!to!
!Drug!Discovery!Across!Gene!Families!
Characterize%ligand%binding%% IdenKfy%offDtargets%by%ligand%%
site%of%primary%target%% binding%site%similarity%
(Geometric%PotenKal)% (Sequence%order%independent%%
profileDprofile%alignment)%
Extract%known%drugs%% %
or%inhibitors%of%the%%
primary%and/or%offDtargets%
Search%for%similar%
small%molecules% …%
Dock%molecules%to%both%%
primary%and%offDtargets%
Xie%and%Bourne%2009%%
Bioinforma2cs$25(12)$305I312%
StaKsKcs%analysis%%
of%docking%score%%
correlaKons%
27
Systems$Pharmacology$–$Example$from$Our$Lab$
Agenda%
SPPS273 1/10/13%
28%
The%Problem%with%Tuberculosis%
• One third of global population infected
• 1.7 million deaths per year
• 95% of deaths in developing countries
• Anti-TB drugs hardly changed in 40 years
• MDR-TB and XDR-TB pose a threat to
human health worldwide
• Development of novel, effective, and
inexpensive drugs is an urgent priority
SPPS273 1/10/13%
29%
Example$1$–$Reposi2oning$The$TB$Story$
Looking%at%the%Problem%on%a%Large%
Scale%
SPPS273 1/10/13%
30%
1. Determine the TB Structural Proteome
Kinnings et al 2010 PLoS Comp Biol 6(11): e1000976
1,%446%
140%
No. of drugs
120%
Acarbose%
100%
Darunavir% AlitreKnoin%
80%
Conjugated%
60% estrogens%
40%
Chenodiol%
Methotrexate%
20%
0%
1% 2% 3% 4% 5% 6% 7% 8% 9% 10%11%12%13%14%15%16%17%18%19%20%21%22%23%24%25%26%27%28%29%30%31%32%33%34%35%36%37%
No.%of%drug%binding%sites%
A Multi-target/drug Strategy
Map 2 onto 1 – The TB-Drugome
http://funsite.sdsc.edu/drugome/TB/
• Entacapone%and%tolcapone%shown%to%have%potenKal%for%
reposiKoning%
• Direct%mechanism%of%acKon%avoids%M.$tuberculosis%
resistance%mechanisms%
• Possess%excellent%safety%profiles%with%few%side%effects%–%
already%on%the%market%
• In$vivo$support%
• Assay%of%direct%binding%of%entacapone%and%tolcapone%to%
InhA%reveals%a%possible%lead%with%no%chemical%relaKonship%
to%exisKng%drugs%
SPPS273 1/10/13%
34%
Example$1$–$Reposi2oning$The$TB$Story$ Kinnings%et%al.%2009%PLoS$Comp$Biol$5(7)%e1000423%
Summary from the TB Alliance –
Medicinal Chemistry
• The%minimal%inhibitory%concentraKon%(MIC)%of%260%
uM%is%higher%than%usually%considered%
• MIC%is%65x%the%esKmated%plasma%concentraKon%
• Have%other%InhA%inhibitors%in%the%pipeline%
SPPS273 1/10/13%
35%
Example$1$–$Reposi2oning$The$TB$Story$ Kinnings%et%al.%2009%PLoS$Comp$Biol$5(7)%e1000423%
New%Ways%of%Thinking%
• Polypharmacology%–%One%or%mulKple%drugs%binding%
to%mulKple%targets%for%a%collecKve%effect%aka%Dirty$
Drugs$
• Network$Pharmacology$–%Measuring%that%effect%on%
the%whole%biological%network%
SPPS273 1/10/13%
36%
Agenda%
SPPS273 1/10/13%
37%
SPPS273 1/10/13%
38%
Example$2$I$The$Torcetrapib$Story$ PLoS$Comp$Biol$$2009$%5(5)%e1000387%
Cholesteryl!Ester!Transfer!Protein%(CETP)%%
CETP%inhibitor%
X
CETP%
LDL% HDL%
Bad%Cholesterol% Good%Cholesterol%
SPPS273 1/10/13%
39%
Example$2$I$The$Torcetrapib$Story$ PLoS$Comp$Biol$$2009$%5(5)%e1000387%
Systems
Pharmacology
Enzyme
inhibition
Uptake ××
× × ×
×
Systemic ×
response
Catalytic Secretion
(or biomass
site components)
Affect protein
Metabolic
function network
Target binding
Drug molecules
Slide from Roger Chang
Multiscale Modeling of Drug
Actions
Understanding of Prediction of molecular
dynamics and interaction network on
kinetics of protein- a genome scale
ligand interactions
Traditional
Approach
physiological!!process!
Reconstruction,
Knowledge analysis and
representation simulation of
and discovery & biological networks
model integration
Systems-based
Approach
Motivators
ModificaKons%to%Early%Stage%Drug%Discovery%
OffDtargets% Systems%Approach%
SPPS273 1/10/13%
42%
hep://www.celgene.com/images/celgene_drug_arrow.gif%
Agenda%
SPPS273 1/10/13%
43%
Words%of%CauKon%
• Mistrust%of%computaKonal%approaches%
• BioinformaKcs%was%previously%oversold%
• Omics%was%previously%oversold%
• Openness%is%an%alien%culture%to%drug%
discovery%
SPPS273 1/10/13%
44%
Further%Reading%
• L.%Xie,%L.%Xie,%S.L.%Kinnings%and%P.E.%Bourne%2012%
Novel%ComputaKonal%Approaches%to%
Polypharmacology%as%a%Means%to%Define%Responses%
to%Individual%Drugs,%Annual$Review$of$Pharmacology$
and$Toxicology%52:$361D379%[PDF].%
• And%references%therein%
SPPS273 1/10/13%
45%
[email protected]
!
QuesKons?%
SPPS273 1/10/13%
46%