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Elution buffers: • use low concentrations of the free cofactor, NAD + or NADP + (up to 20 mM), or increase ionic strength up to 2 M NaCl or 1 M KCl. If detergent or denaturing agents have been used during purification, these can also be used in the low and high pH wash buffers. Cleaning Wash 3 times with 2–3 column volumes of buffers, alternating between high pH (0.1 M Tris-HCl, 0.5 M NaCl, pH 8.5) and low pH (0.1 M sodium acetate, 0.5 M NaCl, pH 4.5). Re-equilibrate immediately with 3–5 column volumes of binding buffer. Remove denatured proteins or lipids by washing with 2 column volumes of 6 M guanidine hydrochloride or 8 M urea. Alternatively, wash the column with 2 column volumes of detergent in a basic or acidic solution, e.g. 0.1% Triton X-100 in 1 M acetic acid. Remove residual detergent by washing with 5 column volumes of 70% ethanol. In both cases wash immediately with 5 column volumes of binding buffer. Media characteristics Ligand and density Composition pH stability* Mean particle size Red Sepharose CL-6B Procion Red HE 3B Ligand coupled to Short term 3–13 90 µm 2 µmoles/ml Sepharose CL-6B using Long term 4–12 the triazine method. *Long term refers to the pH interval over which the medium is stable over a long period of time without adverse effects on its subsequent chromatographic performance. Short term refers to the pH interval for regeneration, cleaning-in-place and sanitization procedures. Chemical stability Stable with all commonly used aqueous buffers and additives such as 8 M urea and 6 M guanidine hydrochloride. Storage Store freeze-dried powders under dry conditions and below +8 °C. Wash media and columns with 20% ethanol in 0.1 M KH 2 PO 4 , pH 8.0 (use approximately 5 column volumes for packed media) and store at +4 to +8 °C. 78
Glycoproteins or polysaccharides Con A Sepharose 4B, Lentil Lectin Sepharose 4B, Agarose Wheat Germ Lectin Glycoproteins and polysaccharides react reversibly, via specific sugar residues, with a group of proteins known as lectins. As ligands for purification media, lectins are used to isolate and separate glycoproteins, glycolipids, polysaccharides, subcellular particles and cells, and to purify detergentsolubilized cell membrane components. Substances bound to the lectin are resolved by using a gradient of ionic strength or of a competitive binding substance. Media screening To select the optimum lectin for purification, it may be necessary to screen different media. The ligands, Concanavalin A (Con A), Lentil Lectin and Wheat Germ Lectin provide a spectrum of parameters for the separation of glycoproteins. Table 5 gives their specificity. Table 5. Specificity of lectins. Lectin Mannose/glucose binding lectins Con A, Canavalia ensiformis Lentil Lectin, Lens culinaris N-acetylglucosamine binding lectins Wheat Germ Lectin, Triticum vulgare Specificity Branched mannoses, carbohydrates with terminal mannose or glucose (aMan > aGlc > GlcNAc). Branched mannoses with fucose linked a(1,6) to N-acetyl-glucosamine, (aMan > aGlc > GlcNAc). Chitobiose core of N-linked oligosaccharides, [GlcNAc(b1,4GlcNAc) 1–2 > bGlcNac]. Con A for binding of branched mannoses, carbohydrates with terminal mannose or glucose (aMan > aGlc > GlcNAc) Concanavalin A (Con A) is a tetrameric metalloprotein isolated from Canavalia ensiformis (jack bean). Con A binds molecules containing a-D-mannopyranosyl, a-D-glucopyranosyl and sterically related residues. The binding sugar requires the presence of C-3, C-4 and C-5 hydroxyl groups for reaction with Con A. Con A can be used for applications such as: • Separation and purification of glycoproteins, polysaccharides and glycolipids. • Detection of changes in composition of carbohydrate-containing substances, e.g. during development. • Isolation of cell surface glycoproteins from detergent-solubilized membranes. • Separation of membrane vesicles into "inside out" and "right side out" fractions. 79
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Affinity Chromatography Principles
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Affinity Chromatography Principles
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Serine proteases and zymogens with
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Appendix 4 ........................
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This handbook describes the role of
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Affinity chromatography is also use
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BioProcess Media for large-scale pr
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Chapter 2 Affinity chromatography i
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Avoid using magnetic stirrers as th
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pH elution A change in pH alters th
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0.6 0.4 0.2 0 A280 pH selected for
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Situation Cause Remedy Protein does
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Chapter 3 Purification of specific
Page 29 and 30: Table 2. Relative binding strengths
Page 31 and 32: Purification examples Figure 11 sho
Page 33 and 34: MAbTrap Kit Fig. 13. MAbTrap Kit, r
Page 35 and 36: Media characteristics Ligand Compos
Page 37 and 38: A 280 nm 2.0 1.5 1.0 0.5 Column: rP
Page 39 and 40: Desalt and/or transfer purified IgG
Page 41 and 42: Performing a separation Column: Rec
Page 43 and 44: M r 97 000 66 000 45 000 30 000 20
Page 45 and 46: in The Recombinant Protein Handbook
Page 47 and 48: Cleaning These procedures are appli
Page 49 and 50: Purification examples Figures 24 an
Page 51 and 52: Nickel solution: 0.1 M NiSO 4 Bindi
Page 53 and 54: Protein A fusion proteins IgG Sepha
Page 55 and 56: Purification or removal of serine p
Page 57 and 58: Sample: 2 ml clarified E. coli homo
Page 59 and 60: Serine proteases and zymogens with
Page 61 and 62: DNA binding proteins HiTrap Heparin
Page 63 and 64: Sample: Column: Binding buffer: Elu
Page 65 and 66: Media characteristics Ligand densit
Page 67 and 68: Sample: Pooled and frozen human pla
Page 69 and 70: The harsh conditions required to br
Page 71 and 72: Purification or removal of albumin
Page 73 and 74: IFN-act. A units 280 nm 250 0.12 20
Page 75 and 76: Purification options Binding capaci
Page 77 and 78: Sepharose NH (CH 2) n NH N N O N N
Page 79: If detergent or denaturing agents h
Page 83 and 84: For complex samples containing glyc
Page 85 and 86: For complex samples containing glyc
Page 87 and 88: Chemical stability Avoid exposure t
Page 89 and 90: Proteins and peptides with exposed
Page 91 and 92: Several methods can be used to dete
Page 93 and 94: Media characteristics Composition M
Page 95 and 96: Performing a separation Binding buf
Page 97 and 98: Do not store the suspension for lon
Page 99 and 100: Sepharose has been modified and dev
Page 101 and 102: Ligand coupling Several methods are
Page 103 and 104: Couple a ligand through the least c
Page 105 and 106: Table 9 summarizes recommended liga
Page 107 and 108: Coupling through the primary amine
Page 109 and 110: Ligand and column preparation 1. Di
Page 111 and 112: Options Product Spacer Coupling con
Page 113 and 114: 100 80 Coupled substance, % 60 40 2
Page 115 and 116: Coupling small ligands through amin
Page 117 and 118: Ligand coupling 1. Add the ligand s
Page 119 and 120: Alternative coupling solutions: Dis
Page 121 and 122: Media characteristics Product Compo
Page 123 and 124: Ligands containing amino groups can
Page 125 and 126: Chapter 6 Affinity chromatography a
Page 127 and 128: Resolution is achieved by the selec
Page 129 and 130: For any capture step, select the te
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Appendix 1 Sample preparation Sampl
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Remove salts from proteins with mol
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1. Filter (0.45 µm) or centrifuge
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For laboratory scale operations, Ta
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Removal of lipoproteins Lipoprotein
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Appendix 2 Selection of purificatio
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4. Estimate the amount of slurry (r
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Appendix 5 Conversion data: protein
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Middle unit residue (-H 2 0) Charge
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Expected results when changing cond
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Expected results with competitive e
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Appendix 8 Analytical assays during
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Appendix 9 Storage of biological sa
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Ordering information Product Quanti
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STREAMLINE, Sepharose, HiTrap, ÄKT
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