亲和原理篇.pptx
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1、内容1.原理什么是亲和层析?亲和层析是通过生物分子的生物相互作用进行生物分子分离的一项液相分离技术。1.平衡平衡2.上样3.结合/洗涤4.洗脱平衡层析柱至可以结合样品的状态凝胶基架特异结合配基亲和层析亲和层析结合目标洗涤杂质在可结合状态结合样品1.平衡2.上样上样3.结合结合/洗涤洗涤4.洗脱亲和层析的主要步骤平衡:让亲和填料处于可以结合目标物的状态上样:将样品通过填料,洗出不结合的杂质洗脱:解吸附,洗脱下目标产物恢复:重新平衡使填料处于可以结合目标物的状态亲和层析EquilibrationSample applicationWashElutionRe-equilibration亲和层析的主要
2、步骤亲和层析亲和层析特点亲和层析特点容易纯化一些别的方法不能分离的蛋白比如:从变性的蛋白中分离天然蛋白及其不同功能的亚型经常一步可用大于95%的纯度从大量杂质中分离高纯度的目标物质可以特异性的去除杂质非常快速亲和层析2.凝胶及其应用配基:特异性的和目标物结合的基团基架:可以和配基耦合的内部填料耦合:配基和基架之间的共价结合结合:配基和目标产物之间的结合亲和层析中的术语亲和填料金属螯合:金属螯合:可反复螯合不同金属,再用已结合依赖不同金属的蛋 白,一种介质可做多种纯化工作活化偶联:最常用的是NHS activated 4 Fast Flow 和CNBr activated 4 FF小配体亲和:纯
3、化抗凝血酶III,凝血因子脂酶等抗体亲和:抗体亲和:颜料亲和:纯化白蛋白,干扰素等外源凝集素亲和:刀豆球蛋白A-多糖,糖蛋白等核酸亲和金属螯合可用反复螯合不同金属,再结合依赖不同金属的蛋白。(His组氨酸、Cys半光氨酸、Try色氨酸)填料类型:IMAC Sepharose:固定化金属离子亲和层析填料,基架已经活化好了,可用于直接耦合金属离子。Ni Sepharose:已经耦合了Ni离子,可以直接用于纯化His蛋白,载量极高,脱落极低。Chelating Sepharose:亚氨双乙酸耦合的填料,可用结合不同的金属离子,脱落低。(详细介绍请参考Tag-protein.ppt)NHS-activ
4、ated Sepharose High Performance12-atom hydrophilic spacer arm to couple via amino groups.NHS-activated Sepharose 4 Fast FlowAs above.CNBr-activated Sepharose 4 Fast FlowCoupling via primary amino groups.EAH Sepharose 4B10-atom spacer arms to couple via amino groups.ECH Sepharose 4B9-atom spacer arms
5、 to couple via carboxyl groups.Epoxy-activated Sepharose 6B12-atom hydrophilic spacer arm to couple through hydroxyl,amino or thiol groups.Activated Thiol Sepharose 4B10-atom spacer arm for reversible coupling through freethiol groups.Thiopropyl Sepharose 6B4-atom hydrophilic spacer arm for reversib
6、le coupling of proteinsand small thiolated ligands through thiol groups.Also reacts withheavy metal ions,alkyl and aryl halides and undergoes additionreactions with compounds containing C=O,C=C and N=N bonds.最常用的是NHS activated 4 Fast Flow 和CNBr activated 4 FF填料类型:活化偶联亲和填料耦合方法1(2)Chemical groupLength
7、 ofStructure ofProducton ligandspacer armspacer armProteins,peptides,amino acidsamino10-atomHiTrap NHS-activated HPNHS-activated Sepharose 4 Fast FlowNoneCNBr-activated Sepharose 4BCNBr-activated Sepharose 4 Fast Flow10-atomECH Sepharose 4Bcarboxyl11-atomEAH Sepharose 4Bthiol4-atomThiopropyl Sepharo
8、se 6B10-atomActivated Thiol Sepharose 4B 12-atomEpoxy-activated Sepharose 6BONOHOONOOONOHOHOONOHNH2OSOHSNNNSOSNNOHOOOHOOOOOHO活化偶联亲和填料Chemical groupLength ofStructure ofProducton ligandspacer arm spacer armSugarshydroxyl12-atomEpoxy-activated Sepharose 6Bamino10-atomHiTrap NHS-activated HP10-atomECH
9、Sepharose 4B12-atomEpoxy-activated Sepharose 6Bcarboxyl11-atomEAH Sepharose 4BOOOOHOONOHOONOOONOHOHOPolynucleotidesaminoNoneCNBr-activated Sepharose 4BCNBr-activated Sepharose 4 Fast Flowmercurated base4-atomThiopropyl Sepharose 6BCoenzymes,cofactors,antibiotics,steroidsamino,carboxyl,thiol or hydro
10、xyl use matrix with spacer arm(see above)OOOOHOONOHNH2OSOHSN耦合方法2(2)活化偶联亲和填料ProductSpacerCouplingMaximumCommentsarmconditions operating flowHiTrap NHS-activated HP 10-atompH 6.59,1530 min.,4 ml/min Pre-activated medium+4 C room temp.(1 ml column)for coupling via 20 ml/min primary amine group(5 ml co
11、lumn)of a ligand.Prepacked 1 ml and 5 ml columns.NHS-activated 10-atompH 69,216 hours,300 cm/h*Supplied as a Sepharose 4 Fast Flow+4 C room temp.suspension ready for column packing.活化偶联亲和填料ProductLigand CompositionpH stability*Mean particle density sizeHiTrap 10 moles/ml6-aminohexanoic acidShort ter
12、m 31234 mNHS-activated HP linked by epoxy coupling to Long term 312highly cross linked agarose,terminal carboxyl group esterified with NHS.NHS-activated 1623 moles/ml As aboveShort term 31390 mSepharose 4Long term 313Fast Flow NHS-activatedOOOH+RCO52222CH(CH)NHNHOOCHCHNOOOHCR5222CH(CH)NHNH+HOOCHCHNO
13、SepharoseSepharose活化偶联亲和填料NHS-activatedReady in less than 15 minutesProtein coupled(mg)Protein added(mg/1 ml column)4030201020406080100Mouse IgG on HiTrap NHS-activated HP,1 ml20406080100 mlLane 1.Eluted material,non-reducedLane 2.LM W Calibration Kit,reduced1 2Mr97 00066 00045 00030 00020 10014 000
14、1 2Mr97 00066 00045 00030 00020 10014 0002.01.0A280 nmFlow through materialNHS-activated活化偶联亲和填料ProductSpacerCouplingMaximumCommentsarmconditionsoperating flowCNBr-activatedNonepH 79,216 hours,400 cm/h*Supplied as a freeze-Sepharose 4 Fast Flow+4 C room temp.dried powder.CNBr-activatedNonepH 810,216
15、 hours,75 cm/h*Supplied as a freeze-Sepharose 4B+4 C room temp.dried powder.ProductCompositionBinding capacitypH stability*Mean particleper ml mediumsizeCNBr-activatedCyanogen bromide reactsa-chymotrypsinogen,Short term 31190 mSepharose 4 Fast Flowwith hydroxyl groups on1326 mgLong term 311Sepharose
16、 to give aCNBr-activatedreactive product fora-chymotrypsinogen,Short term 211Sepharose 4Bcoupling ligands via2560 mgLong term 211primary amino groups orsimilar nucleophilic groups.活化偶联亲和填料CNBr-activatedCNHisoureaNHRCNBrRNH2OOHOHHOSepharoseSepharoseCNBr-activated活化偶联亲和填料CNBr-activated Sepharose 4B wa
17、shed at pH 3 and transferred to 0.1 M NaHCO3,pH 8.3 for pre-hydrolysis.Samples removed after different times and tested for coupling activity towards a a-chymotrypsinogen(A)and glycyl-leucine(B).glyleuTime of pre-hydrolysis,hours02134204060010024ABAB80Coupled substance,%a-chymotrypsinogenA280 nm0.50
18、24 hours40 minTimenative gp120Lectin coupled to CNBr-activated Sepharose 4 Fast Flow活化偶联亲和填料CNBr-activatedProductSpacerSubstitutionCouplingMaximum Commentsarmper ml matrixconditionsoperatingflowEAH Sepharose 4B10-atom711 molespH 4.5,1.524 hours,75 cm/hCouple ligands amino+4 C room temp.containing fr
19、ee groupscarboxyl groups.Supplied as a suspension ready for use.ECH Sepharose 4B9-atom1216 molespH 4.5,1.524 hours,75 cm/hCouple ligands carboxyl+4 C room temp.containing free groupsamino groups.Supplied as a suspension ready for use.ProductCompositionpH stability Mean particle size EAH Sepharose 4B
20、Covalent linkage of 1,6-diamino-hexaneShort term 31490 mby epoxy coupling creates a stable,Long term 314uncharged ether link between a 10-atomspacer arm and Sepharose 4B.ECH Sepharose 4BCovalent linkage of 6-aminohexanoic acidShort term 31490 mby epoxy coupling creates a stable,Long term 314uncharge
21、d ether link between the 9-atom spacer arm and Sepharose 4B.活化偶联亲和填料ECH&EAH Sepharose SepharoseOHCOOH5222CH(CH)NHO CHCHOHNH62222CH(CH)NHO CHCHSepharosePartial structuresECH Sepharose 4BEAH Sepharose 4BPartial structures活化偶联亲和填料ECH&EAH Sepharose ProductSpacerSubstitution CouplingMaximum Commentsarmpe
22、r ml matrixconditionsoperatingflowEpoxy-activated12-atom1940 molespH 913,16 hours 75 cm/hSupplied as aSepharose 6Bepoxy groupsseveral days,freeze-dried+20 +40 C powder.CompositionpH stability Mean particlesizeSepharose 6B reacts withShort term 21490 m1,4 bis-(2,3 epoxypropoxy-)Long term 214butane to
23、 form a stableether linkage.OH422222CHCH(CH)OOOO CHCHCHCHSepharosePartial structureEpoxy-activated Sepharose 6B活化偶联亲和填料Carbonate/bicarbonate buffers pH 911NaOH solution pH 1214.Ligand concentrations:5 and 20 mg/mlN-acetyl-D-galactosamine to Epoxy-activated Sepharose 6B20 mg/ml5 mg/mlpH91011121325507
24、5010014Coupled ligand moles/g conjugateGlycyl-leucine to Epoxy-activated Sepharose 6BpH 10.5,+40 CpH 11.0,+45 CTime hours0816243225507501004048Coupled glycylleucine,%活化偶联亲和填料Epoxy-activated Sepharose 6BMixed disulphide formation(1),reversible by reducing agents such as dithiothreitol(DTT)(2).Mixed d
25、isulphide formation with 2,2-dipyridyl disulphide:2-thiopyridyl derivative for covalent chromatography(3).Reaction with heavy metals and derivatives e.g.p chloromercuribenzoate(4):mercaptide formation.Treatment with alkyl or aryl halides:thioether derivatives(5).Addition reactions(6)with C=O,C=C and
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