the benefits gained from a redesigned crystallisation … benefits gained from a redesigned...
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| 1 RAMC September 2013, Bischenberg
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
Alexey Rak Structure-Design-Informatics Paris LGCR France Sanofi R&D
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Sanofi.com
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Some of Sanofis brands
NO-SPA
Probiotics
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Thanks to SB team at Sanofi R&D France
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Alain Dupuy
Maryse Lowinski Jean-Pierre Marquette
Annick Parent
Valerie Steier
Stephanie Pouzieux
Alexey Rak
Franois Vallee Thomas Bertrand
Magali Mathieu
Laure Delarbre
Alain Dupuy Jacques Houtmann
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The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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The presentation plan
Introduction to MMS technology - microseeding
MMS at Sanofi R&D in France
Experimental details on microseeding plates setup
Examples on small molecules-protein complexes and protein - protein complexes crystallization
Conclusions about time- and cost effectiveness to use MMS in ambitious structural biology labs
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Introduction to MMS technology and the principles of microseeding Protein crystallization is a major bottleneck for protein structure
determination
Protein crystallization still remains the least standard part of the protein structure determination process by X-Ray crystallography
Nucleation is the first and critical step to succeed with protein crystallization
Crystals nuclei (seeds) can be transferred from drop to drop to increase success with 3D growth of crystals
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Introduction to MMS technology and the principles of microseeding The seeding technique was introduced a few decades ago
On page 77 of protein Crystallography by Blundell and Johnson (1979): This method (Vapour diffusion) is particularly effective for growing large
crystals , especially if the drop is seeded No reference given
Successive 10-fold dilution was the standard from crushed crystals for
micro-seeding
Enrico Stura introduced streak seeding and perfected macroseeding for sitting drops and the concepts of how to use seeding to understand where you may be in the phase diagram without actually calculating a phase diagram. This method revolutionized the protein crystallization process
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Introduction to MMS technology and the principles of microseeding Microseed Matrix Seeding MMS
First introduced by C.G. Ireton and B. Stoddard C.G. Ireton and B. Stoddard (2004) Microseed matrix screening to improve
crystals of yeast cytosine deaminase. Acta Cryst. D60, 601-605
Allan DArcy and coworkers expanded this method by automating the procedure and seeding directly into crystallization screens
D'Arcy A, Villard F, Marsh M. An automated microseed matrix-screening method for protein crystallization. Acta Cryst. D63, 550-4. 2007
A more detailed presentation on MMS can be accessed at http://hamptonresearch.com/ramc_2007.aspx?id=1 Allan DArcys presentation at Recent Advances in Macromolecular
Crystallization (RAMC) 2007 San Diego, CA USA
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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http://hamptonresearch.com/ramc_2007.aspx?id=1
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Introduction to MMS technology and the principles of microseeding MMS seeding - transfer of very small crystals seeds to another
crystallization drop can give rise to improve crystal quality
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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The method has been successfully demonstrated to be applicable for general use
Showed success on different classes of proteins In generating new space groups Improving diffraction quality Finding useful hits when there were
none before
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Why Mosquito is highly effective for MMS The Mosquito crystallization robot is very accurate at liquid handling of low
volume solutions 20-100 nL
Mosquito - extremely reliable and robust instrument, more than 10 years personal experience
Disposable tips no cross-contamination and contact dispensing which are both very important instrument features for seeding MMS
Availability of the multi-aspirate dispensing mode for Mosquito pipetting Makes MMS by Mosquito quick and efficient
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Why Mosquito is highly effective for MMS Multi-aspirate dispensing
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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http://www.youtube.com/watch?v=UFDq64vfPFY&list=PLJSU0gmdN4qJFeluG0KiowKZMwUs4NBSM&index=1
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Experimental details on Mosquito assisted microseeding plates setup
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Multi-aspirate dispensing enables the pipetting of two (and more) solutions in conjunction
Solution 1 is a seed stock, solution 2 is a crystallization solution reservoir Put together but not mixed inside of the Mosquito disposable tip
Shaken, not stirred! Solution 1&2 pipetted at destination crystallization drop pedestal which is
preoccupied by protein solution drop
Routinely: (20nL of seeds + 80nL of reservoir) + 100nL of protein
1 33 for single protein 96 well plate - MMS using Mosquito < 5 minutes for three proteins 96 well plate - MMS using Mosquito
288 individual seeded crystallization conditions in less than 5 minutes
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Experimental details on Mosquito assisted microseeding plates setup
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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http://www.youtube.com/watch?v=UFDq64vfPFY&list=PLJSU0gmdN4qJFeluG0KiowKZMwUs4NBSM&index=1
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MMS success rate
Crystallization optimization by seeding enforced screening is shown to be extremely successful by generating new crystal forms during MMS
The number of hits generated by MMS is much grater than in crystallization screening without seeding
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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D'Arcy A, Villard F, Marsh M. An automated microseed matrix-screening method for protein crystallization. Acta Cryst. D63, 550-4. 2007
Sparse matrix screening
The same Sparse matrix screening but with seeding by MMS
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MMS applications and its usefulness MMS is still good for :
Generating new space groups Improving diffraction quality Finding useful hits when there were none before
MMS is also good for : Generating crystals of otherwise non-crystallisable targets:
new shorter or extended construct of the crystallized protein Example will be given
new ligand bound crystal forms of the crystallized protein new proteins using similar but not identical protein crystals
protein family cross seeding protein complex using crystal seeds of one of the complex
component/protein Example will be given
individual proteins using crystals of protein complex where the aimed protein was complexed with another partner
Example will be given
The benefits gained from a redesigned crystallisation
strategy focused on a high throughput seeding technique
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Statistics on small molecules-protein complexes and Ab-Ag complexes crystallization Crystallization optimization by MMS takes the same or less time than the
classical manual crystallization optimization but consumes much less protein Vapor diffusion rate for 100nl + 100nl drops is proportionally higher than
manually performed 1l + 1l 96 conditions by MMS require ~14l of protein solution
(20nL of seeds + 80nL of reservoir) + 100nL of protein 14L of protein is enough to set up manually ~14 crystallization
conditions with micro-seeding It is quicker to set up 96 conditions MMS experiments by Mosquito than
14 crystallization/seeding drops performed manually The most expensive part of crystallization/optimization of medically
relevant human proteins is the cost of the protein itself
Crystallization optimization by MMS is more time- and cost- effective than classical crystallization optimization
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Crystallization optimization, real example
The only crystallization hit obtained
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Classical manual optimization ~ 6 weeks 0.3 FTE 4.5 mg protein The best result 3.2
resolution MMS in 4 x 96 condition
Two sparse matrix and two grid screens used
26 new conditions found resulting crystals of better than initial quality
~ 1 day 1 FTE 0.6 mg protein 1.7 - 2.2 resolution
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Crystallization of different construct representing the same multi-domains protein PI3K beta oncology target
No high resolution structure Despite many efforts
>180 constructs of the heterodimer were expressed 32 constructs submitted to crystallization trials
2 constructs crystallized in classical crystallization screening 19 constructs crystallized in MMS assisted crystallization screening
Seeds of different construct(s) were used to fertilize new construct drops Crystallization optimization was achieved most successfully by MMS
Seeds of the crystallization hits were used to generate new crystals of the same construct
MMS was applied sometimes in several cycles The better seeds result the better crystals
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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150um 150um 50um 50um
MMS MMS
2.6A diffracting Crystals !
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Crystallization of protein complexes, MMS assisted combinatorial approach Need to crystallize multi-domain protein alone and in complex with its
interacting partners
Classical crystallization screening: No crystals for the multi-domain protein alone X No crystals for complex with two partners X No crystals for complex with red partner X Crystals for complex with green partner V
MMS using seeds of the green partner complex crystals to crystallize other combinations of the interest No crystals for complex with two partners X Crystals for multi-domain protein alone V No Crystals for complex with red partner X
MMS using seeds of the multi-domain protein alone crystals to crystallize other combinations of the interest No crystals for complex with two partners X Crystals for complex with red partner V
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Conclusions
Seeding by MMS is very effective method to optimize protein crystals quality and to generate crystals of otherwise non-crystallizable proteins
Miniaturizing MMS is both time- and cost-effective
Automating the process gives speed and reliability
key features needed: multiple aspirations then direct dispense to combine both seed stock and
screen, then add them to the protein no cross-contamination accurate handling of very low volumes
Mosquito has proven to be an essential tool for MMS in Sanofi R&D France labs
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding technique
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Merci
NOM DE LA PRESENTATION | 21
The benefits gained from a redesigned crystallisation strategy focused on a high throughput seeding techniqueSanofi.comSlide Number 3Thanks toSB team at Sanofi R&DFranceThe presentation planIntroduction to MMS technology and the principles of microseedingIntroduction to MMS technology and the principles of microseedingIntroduction to MMS technology and the principles of microseedingIntroduction to MMS technology and the principles of microseedingWhy Mosquito is highly effective for MMSWhy Mosquito is highly effective for MMSMulti-aspirate dispensingExperimental details on Mosquito assisted microseeding plates setupExperimental details on Mosquito assisted microseeding plates setupMMS success rate MMS applications and its usefulnessStatistics on small molecules-protein complexes and Ab-Ag complexes crystallizationCrystallization optimization, real exampleCrystallization of different construct representing the same multi-domains proteinCrystallization of protein complexes, MMS assisted combinatorial approachConclusionsMerci