drug design intro - katedra fyzikální chemie...
TRANSCRIPT
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Karel Berka, Ph.D.
Martin Lepšík, Ph.D.
Pavel Polishchuk, Ph.D.
Thierry Langer, Ph.D.
Jana Vrbková, Ph.D.
3rd Advanced in silico Drug Design
KFC/ADDDrug design intro
UP Olomouc, 23.1.-26.1. 2018
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Motto
A pharmaceutical company utilizing computational drug design is like an organic chemist utilizing an NMR. It won’t solve all of your problems, but you are much better off with it than without it.
DAVID C. YOUNG
Disclaimer:
Authors of this lecture series did not designed any drug in common use.
Yet. 2
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Course ProgramTuesday - basics
• 12:30 Drug design – intro (Berka)
• 13:30 Virtual Screening (Polishchuk)
• 14:30 Statistical learning (Vrbková)
• 16:00 Chemical Libraries (Polishchuk)
• 17:00 Structural bioinfo tools (Berka)
Wednesday – structure-based methods
• 8:30 MM basics (Berka)
• 9:30 Molecular docking intro (Berka)
• 10:40 Tutorial – Mol. docking (Berka)
• 12:00 Lunch break
• 13:00 Advanced Docking (Lepšík)
• 14:00 MD and adv. scoring (Lepšík)
• 15:30 Tutorial - Adv. Docking + MD (Lepšík)
Thursday – Ligand-based methods
• 8:30 QSAR modelling (Polishchuk)
• 9:50 Tutorial – QSAR and similaritysearch (Polishchuk)
• 12:00 Lunch break
• 13:00 Pharmacophores (Langer)
• 14:20 Tutorial - Pharmacophore (Langer)
• 18:00 Workshop dinner
Friday – Challenge/hackathon
• 8:30 Challenge (Polishchuk]
• 15:00 Final word (Berka)
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Ligand challenge
• Hackathon (Friday)
– Drug design for selected problem
– http://158.194.101.252:3838/challenge/
– Selection of active compounds from the blind set
– Participation to hackathon is exam requirement for Advanced Rational Drug Design (4 ECTS credits)
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Literature
• Young, D.C. Computational Drug Design. Wiley, 2009.
• Young D.C. Computational Chemistry, a Practical Guidefor Applying Techniques to Real World Problems. Wiley, 2001.
• Alvarez J. & Shoichet B. (Eds.). Virtual Screening in Drug Discovery. Taylor&Francis, 2005.
• Berka K. & Bazgier V. Racionální návrh léčiv pomocí in silico metod. UP Olomouc, 2015 (in Czech)
• Derek Lowe – In the pipeline blog http://blogs.sciencemag.org/pipeline/
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SOURCES OF DRUGS
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History of Drug Design
1806
A. Cherkasov7
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Time New Sources Testing Subjects
- ancient & plants, poisons (Paracelsus) humansmiddle ages minerals ... natural sources
- 1806 morphine (first extracted) humans- 1850 chemicals (chinin) humans (prisoners)- 1890 synthetics, pigments animals- 1920 animals, isolated organs- 1970-1980 enzymes, cell lines (HeLa)- 1990 High throughput libraries recombinant proteins- 2000 chemical libraries chips, virtual screening,
ADMET testing
History of Drug Design
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All drugs by source, registered 01/1981 - 06/2006, FDA, n = 1184
B – biologicals, N – nature compounds, ND – nature compounds derivatized, S – synthetic compounds,
S/NM – synthetics mimicking natural compounds, S* - synthetic, with pharmacophore from natural compoundsV - vaccines
Sources of Drugs
D. J. Newman and G. M. Cragg, J. Nat. Prod. 70, 461-477 (2007)
S; 30%
ND; 23%B; 14%
S/NM; 10%
S*/NM; 10%
N; 5%S*; 4% V; 4%
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Idealized Drug Design ProjectIllness
Isolation of
cause
(many years)
Identification of
lead compound
(2-5 let)
Preclinical
testing on
animals
(1-3 years)
Formulation
(1-3 years)
Human clinical trials
(2-10 years)
FDA approval
(2-3 years)
Heal and Sell10
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Vocabulary• Target
– Biomolecule interacting with the drug
• Lead– Base molecular structural motif of developed drug
• Hit– Compound with positive hit in initial screening
• Candidate compounds– Selected compounds used for next testing
• Efficacy– Qualitative property – (drug heals or not)
• Activity– Quantitative property – dosage needed for effect to happen
(pM – great, nM – excellent, μM – sufficient, mM – well…)
• Bioavailability– Availability of compound in site of target in necessary concentration
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Eroom’s Law
Scannell JW, Blanckley A, Boldon H, Warrington B: Nature Reviews Drug Discovery 11, 191-200 (2012) doi:10.1038/nrd3681
• Decline in pharmaceutical R&D efficiency –halved per 9 years– 'better than the Beatles' problem
– 'cautious regulator' problem
– 'throw money at it' tendency
– 'basic research–brute force' bias.12
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DRUG DESIGN
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Drug DesignIdentification of new drug:
• Expensive problem
– Expenditures per 1 drug development - 1 300 000 000 USD1
+ expenses for production, patents, distribution…
New drugs are expensive >1 000 USD/dose of drug2
• Hard problem
– Identification of target-drug pair is not simple
– ADMET
– Side-effects
1 - Tufts Center for the Study of Drug Development, 20122 – SÚKL, 3Q 2011, average price tag for most expensive drug category in CZ (over 10kCZK)
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Expensive Problem
David C. Young - Computational Drug Design: A guide for computational and medicinal chemists. Wiley-Blackwell, New York, 2009, ISBN 978-0470126851
Experiment Cost per 1 compound
Virtual screening 100 CZK
Biochemical analysis 7 000 CZK
Cell culture testing 75 000 CZK
Acute toxicity on mice 250 000 CZK
Protein structure evaluation with X-Ray 2 000 000 CZK
Efficiency testing on animals 5 500 000 CZK
Chronic toxicity on rats 14 000 000 CZK
Clinical testing on volunteers 10 000 000 000 CZK
Lower price tag allow testing of more drug candidates
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Hard Problem• Human genom ~25 000 ORF- Alternative splicing => ~500 000 proteins ~ 38 000 structures known human in PDB (13 000 unique)- RNA role- protein protein interactions role
• 2 – 10 years from lead molecule identification to clinical testing (patents last 20 years)
• 1 successful out of 10 drug development projects
www.rcsb.org - 23.1.2016 16
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Possible Obstacles• Nonexistent testing model
– Example: HIV is human disease!– Ethically not possible to test directly on people (cf. OS)
• Rare disease – orphan disease– Future sales would not pay for regular development– Orphan drug have lower requirements for registration
and individual incentives
• Too low activity of found drug– Too toxic, bad bioavailability
• Active compounds are already patented– Me2drugs– Product has to be just as good as the one from
competition and patentable under our name
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Illness Type • Enzyme overproduction - some cancer types
– Inhibition (e.g. kinase inhibitors)
• High response of receptor – COX in pain– Antagonists (e.g. pain relievers)
• Low response of receptor – neurological GPCRs– Agonists (e.g. serotonin receptor agonists)
• Regulation peptide – CGRP peptide in migraine– Antibodies (e.g. biologicals)
• RNA – RNAi, RNA aptamers… – Emerging field
Small ligand with protein 18
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Most Typical Mechanism of Drug Action
• Lock and Key Analogon, 1894
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DRUG TARGETS
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Drug Targets
R. Santos, …, JP Overington: A comprehensive map of molecular drug targets. Nature Rev. Drug Discovery, 16, 19-34, 2017. doi: 10.1038/nrd.2016.230
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ATC code• The Anatomical Therapeutic Chemical Classification System
code (ATC code) is attributed to a drug by the WHO Collaborating Centre (WHOCC) for Drug Statistics Methodology. – Level 1 – organ - (G): genito urinary system and sex hormones
– Level 2 – pharmacological action - (G04): urologicals
– Level 3 – pharmacological subgroup (G04B): urologicals
– Level4 – pharmacological subsubgroup (G04BE): in erectile dysfunction
– Level 5 - specific drug or combination (G04BE03): sildenafil
• a drug can have multiple codes,
– aspirin (B01AC06, A01AD05, N02BA01, N02BA51 and N02BA71)
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Drugs by ATC code
R. Santos, …, JP Overington: A comprehensive map of molecular drug targets. Nature Rev. Drug Discovery, 16, 19-34, 2017. doi: 10.1038/nrd.2016.230
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Drug Targets by ATC
R. Santos, …, JP Overington: A comprehensive map of molecular drug targets. Nature Rev. Drug Discovery, 16, 19-34, 2017. doi: 10.1038/nrd.2016.230
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Drug Target Types
Di Meo F, Fabre G, Berka K, Ossman T, Chantemargue B, Paloncýová M, Marquet P, Otyepka M, Trouillas P: In Silico Pharmacology: Drug Membrane Partitioning and Crossing. Pharmacol. Res., 111, 471–486, 2016.
> 60% membranebound
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R. Santos, …, JP Overington: A comprehensive map of molecular drug targets. Nature Rev. Drug Discovery, 16, 19-34, 2017. doi: 10.1038/nrd.2016.230
FURTHER INFORMATION canSAR: https://cansar.icr.ac.uk ChEMBL: https://www.ebi.ac.uk/chembl Companion diagnostic test: http://www.fda.gov/companiondiagnostics Dronedarone prescribing information: http://www.accessdata.fda.gov/drugsatfda_docs/ label/2013/022425s021lbl.pdf DrugCentral: http://drugcentral.org Illuminating the Druggable Genome: https://pharos.nih.gov/idg/indexIUPHAR/BPS Guide to Pharmacology: http://www.guidetopharmacology.org/GRACNCATS Pharmaceutical Collection: https://tripod.nih.gov/npc/ ATC/DDD Index: http://www.whocc.no/atc_ddd_index WHO INN Drug lists: http://www.who.int/medicines/ publications/druginformation/innlists/en
Innovation Patterns in Privileged Classes
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SMALL MOLECULES
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Possibilities of in silico Drug Design
Known ligand Unknown ligandK
no
wn
targ
et
str
uctu
re
Un
kn
ow
nta
rge
t
str
uctu
re
Structure-based drug design
(SBDD)
Docking
Ligand-based drug design
(LBDD)
1 or more ligands
• Similarity search
Several ligands
• Pharmacophore
Large number of ligands (20+)
• Quantitative Structure-Activity
Relationships (QSAR)
De novo design
CADD not possible
some experimental
data needed
ADMET filtering
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BIOLOGICALS
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Definition of Biological Product• US:
– The term “biological product” or biologics means a "any virus, therapeutic serum, toxin, antitoxin or analogous product applicable to the prevention, treatment or cure of diseases or injuries of man“
• EU:
– 'biological medicinal products' as "a protein or nucleic acid–based pharmaceutical substance used for therapeutic or in vivo diagnostic purposes, which is produced by means other than direct extraction from a native (nonengineered) biological source"
30Ronald A Rader (Re)defining biopharmaceutical Nature Biotechnology 26, 743 - 751 (2008) doi:10.1038/nbt0708-743 30
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Small Molecules vz BiologicalsChemical medicines are chemicals made by chemists out of other chemicals
Biologics are grown from living things Biologics are highly sensitive to manufacturing conditions
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32C. Thomas Caskey, Annu. Rev. Med. 2007. 58:1–16
FDA Approved New Chemical Entities
and Biological Derivatives
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What are Biologicals?
• made of sugars, proteins, or nucleic acids or complex combinations of these substances, or may be living entities such as cells and tissues
• Like drugs, biological products are used to either:
– treat or cure diseases and medical conditions,
– prevent diseases, or
– diagnose diseases
• Biological products are made from a variety of natural sources.
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Types of Biological Products
• Blood Derivatives• Whole Blood• Blood Components• Proteins• Human Tissues• Xenotransplantation Products• Cellular & Gene Therapies• Vaccines• Allergenic Extracts
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Size and Complexity of Biologicals in Comparison with Small Molecules
Aspirin 180 Da
Monoclonal Antibody ~150,000 Da
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Protein Function Depend on FinalConfiguration
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Rational Protein Drug Design
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TAKE HOME MESSAGE
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Take Home Message
• Drugs comes from various sources
• Drug design is hard and expensive problem
– Mainly due to the biology!
• Most typical drug targets are:
– GPCRs, ion channels, nuclear receptors, kinases
– But - long tail of other drug targets
• Biologicals are more complex than small molecules
• There is no gold path for drug design – the methods have to be tied up to the current project