Lecture 2. Crystals: Theory and Practice. Dr. Susan Yates Wednesday, February 2, 2011
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1 Lecture 2 Crystals: Theory and Practice Dr. Susan Yates Wednesday, February 2, 2011
2 Steps in Solving an X-ray Structure
3 What is a Crystal? Crystal acts as an X-ray diffraction amplifier
4 Crystals Crystals consist of a structural motif, repeated at regular spacings Unit cell The smallest repeating unit that can generate the entire crystal using only translation operations Mathematical concept - one molecule does not need to fit neatly in this box
5 Lattice Crystal Lattice The set of points in the crystal that are equivalent to each other Geometric arrangement of the points in space at which the atoms/molecules/ions of a crystal occur
6 Crystal Lattice
7 Precipitating Proteins In a concentrated protein solution, proteins interact with water and with other proteins Proteins stay in solution as long as the interactions they make with water are energetically more favourable than those they make with other proteins If you alter this equilibrium (e.g. by competing water away using high salt concentrations - salting out), proteins start to bind one another and precipitate
8 Protein Precipitation When a precipitation agent is added to a concentrated protein solution, protein-protein interactions become energetically more favourable than protein-solvent interactions Proteins bind one another and come out of solution No preferred way that the proteins interact Result is a precipitate with no long range order
9 Protein Crystallization Crystallization differs from precipitation because each molecule in the precipitate interacts with its neighbours in the same way as every other molecule The result is a highly ordered arrangement - a crystal
10 Crystallizing a Protein Growing a protein crystal requires controlled precipitation Interactions between individual protein molecules in a crystal are stabilized by energetically favourable contacts The forces involved include hydrogen bonds, salt bridges, hydrophobic effect etc. Tricky to find this condition and prevent formation of non-specific aggregates
11 Energy Barrier to Crystallization favourable G= H-T S unfavourable crystal represents the lowest freeenergy
12 Crystallization: Solubility Protein solubility varies with the concentration of salts, polyethylene glycols and other substances in the protein solution A protein will quickly form an amorphous precipitate if the solubility is lowered drastically A protein might crystallize if the concentration is slightly above the solubility limit
13 Crystallization Phase Diagram Crystallization Clear
14 Crystallization Process Productive crystallization process fluctuates between Nucleation and Clear zones, largely due to decreased protein concentration since protein sample is consumed in crystal formation
15 Salts Crystallizing Agents e.g. Sulfates, phosphates Long chain organic polymers Polyethylene glycols (PEG) Organic solvents Generally hydrophilic alcohols, ethers or ketones e.g. Methyl-pentanediol, isopropanol
16 Methods to Precipitate a Protein High salt The salt ions order water molecules around them, leaving less unstructured water to solubilize the protein Organic solvents These effectively dilute water with a less polar, less H- bond capable solvent with lower dielectric etc. Long chain organic polymers PEG prefers to writhe over a large volume of space Taking the protein out of solution frees up more space for PEG and is energetically favoured
17 Other Factors Influencing Crystallization Protein concentration ph Need less precipitant to precipitate the more concentrated the protein Changing the ph adds/removes protons from individual residues, possibly creating new salt bridges/h-bonds Temperature As temperature changes, so do the enthalpic and entropic contributions to G crystallization Presence of ligands Ligands may lock the protein into one conformation, which can help crystallization
18 Vapour Diffusion Small volumes of precipitant and protein mixed together into a drop which is equilibrated against a larger reservoir of solution containing precipitant or dehydrating agent Reservoir or crystallization solution can be a mixture of many combinations Buffer (type and conc), ph, precipitant (type and conc), temperature, protein conc, ionic strength etc. Hanging drop Sitting drop
19 Vapour Diffusion
20 Slowly increases protein and precipitant concentrations 12 h to 4 days to equilibrate Mix protein solution with precipitant solution (1:1) and equilibrate against excess of the latter Need 1 µl of 10 mg/ml protein solution per experiment (well) Vapour Diffusion
21 Typical Crystallization Procedures Screening Start with commercial screening kits derived from extensive practical experience; there are hundreds mixtures covering wide range of conditions Optimization Once a lead condition is found from the screening process, expansion (ph and concentration of precipitant etc.) will be carried out Small crystals Culture plate Micro-crystals Good single (~ mm)
22 The Practicalities of Growing Macromolecule Crystals If you are lucky half of all your protein constructs will crystallize
23 Crystal Screening Combinations of precipitating agents and factors that might lead to a crystal is near infinite A typical protein will only crystallize in a small fraction of these conditions When screening you look for crystal leads Anything that appears crystalline Unlikely to get big, picture perfect crystals Not all proteins crystallize! Often you have to go back, purify your protein further, make a new construct
24 Finding Initial Conditions Check crystal set-ups every day in first week Possible results Clear, precipitate, crystal and many others (turbid, bubbles, clothing fibers) If almost all or almost no drops are clear, raise or lower protein concentration, respectively Focus on set-ups that show some precipitate, but not a heavy yellow or brown precipitate indicative of protein denaturation
25 Crystal Refinement Refinement is the process by which known crystals are improved once initial crystals have been found by screening Fine-tuning the conditions Changing the PEG concentration from 30% to 35% Increasing the ph from 5.5 to 6.5 Adding 4% glycerol Increasing salt concentration from 200 mm to 300 mm The process is generally iterative Stop when the crystals are single and big enough to undergo diffraction testing ( µm)
26 Improving Size and Diffraction Systematic variation of all concentrations and ph Additive screens and detergent screens Temperature Seeding with crushed crystals (micro seeding) Dialysis, batch, sitting drop check old set-ups for different crystal form
27 Crystallization Examples Lysozyme 100 mg/ml protein in 50 mm sodium acetate ph % (w/v) PEG 5000, 1.0 M NaCl, 50 mm sodium acetate ph 4.5 Glucose isomerase mg/ml protein in water or 50 mm buffer ph M ammonium sulfate ph 6-9
28 Crystal Growth Lysozyme crystal growth in a few hours time Most will take days to weeks
29 Example of a Protein Crystal The contacts between molecules are generally tenuous, involving only a handful of residues Protein crystals contain large solvent channels, typically making up 40% - 70% of its volume The crystalline order is destroyed by exposing a crystal to air (solvent evaporates) or to mechanical stress (behaves somewhat like watermelon flesh)
30 Crystal Galleries Dust/fibre assisted nucleation
31 Crystal Galleries
32 Crystal Galleries
33 Things in Drops (Other than Crystals) Clear Junk Skins Ppt (Hope) Ppt (No Hope) Phase Separation
34 It Will Not Crystallize Check purity and stability Remove cysteins and other trouble makers Remove flexible parts Try single domains Try physiologically relevant complexes Be creative!
35 Truth Behind Crystallization
36 Obtaining Well-Diffracting Crystals Take-home message Getting a crystal can be hard Goal Three-dimensional single crystal A good protein sample Principles of crystal growth Crystallization techniques Strategies to obtain well-diffracting crystals (quickly?) Practical considerations
37 Small Molecule and Large Crystal The world's largest (701 lbs) fast-growth crystal, grown at Lawrence Livermore National Laboratory The pyramid-shaped potassium dihydrogen phosphate crystal measures ~26x21x23 The enormous crystal was sliced into ½ thick plates and used in a giant laser that will help maintain the safety and reliability of the nation's nuclear weapons stockpile
38 Instrumentation Next time Waves and Diffraction
Steps in solving a structure. Diffraction experiment. Obtaining well-diffracting crystals. Three dimensional crystals
Protein structure from X-ray diffraction Diffraction images: ciprocal space Protein, chemical structure: IALEFGPSLKMNE Conformation, 3D-structure: CRYST1 221.200 73.600 80.900 90.00 90.00 90.00 P 21 21
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