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liguofu§3ProteinStructureConjugatedprotein:consistsofAAsandothers(Native)ProteinSimpleprotein:onlyconsistsofAAsApoprotein+prostheticgroupliguofuTheseproteinsarereferredasconjugatedproteinswhiletheaminoacidpartaloneiscalledapoprotein.liguofu§3ProteinStructure§3.1PrimaryStructure§3.2SecondaryStructure§3.3Tertiary&QuaternaryStructure§3.4Folding,Unfolding&Refoldingliguofu§3.1PrimaryStructureRelatedconceptsStructuralfeaturesHomology(同源性)liguofuRelatedconceptsPeptidebond/肽鍵:~1000yearsinH2OwithoutcatalystPeptidebond/肽鍵:~1000yearsinH2OwithoutcatalystPeptidebond/肽鍵:~1000yearsinH2OwithoutcatalystSidechain側(cè)鏈C-terminalC-末端N-terminalN-末端Residue/氨基酸殘基:Itsaveragemolecularweightis110statisticallyestimatedbytheoccurrenceof20AAsinnaturalproteinsliguofuRelatedconcepts(ctnd)Oligopeptides/寡聚肽:lessthan50aaresiduesPolypeptides/多肽:btw50-10aaresiduesProtein/蛋白質(zhì):morethan100aaresiduesEachpeptidehasacharacteristictitrationcurveandan
isoelectricpoint(pI).liguofuPeptidebondisrigidandplanar1.49?1.27?1.32?Structuralfeatures(ctnd)liguofuc)=0o,=0o;itisdisallowedbythestericoverlapbetweenHandOatomsofadjacentpeptideplanes.b)=180o,=180o;thepeptideisinitsfullyextendedconformation.Structuralfeatures(ctnd)liguofuRamachandranplotforL-AlaresiduesDarkblue:nostericoverlapandfullyallowed;mediumblue:attheextremelimitsforunfavorableatomiccontacts;lightestblue:permissibleifalittleflexibilityisallowedStructuralfeatures(ctnd)liguofuHomologyHomologousproteins:evolutionarilyrelated;performthesamefunctionindifferentspeciesInvariantresidues:Manypositionsinprimarystructureareoccupiedbythesameaaresiduesinallspecies.
Variableresidues:OtherpositionsinprimarystructureareoccupiedbydifferentaaresiduesindifferentspeciesConservativesubstitutions:Insomepositions,allsubstitutionsinvolvesimilaraaresidues(e.g.,Arg?Lys,bothofwhicharepositivelycharged).InvariantHomology(cntd,sequenceofcytochromec)liguofu馬細胞色素c的空間結(jié)構(gòu)Homology(cntd)馬與金槍魚細胞色素c的空間結(jié)構(gòu)比較liguofuHomology(cntd)liguofu§3.2SecondaryStructure1.
a-helixa-chain2.
b-pleatedsheet3.
bturnLoopRandomcoilliguofu1.
a-helixproposedbyPaulingandCoreyin1951liguofuliguofuliguofu第n個氨基酸a-氨基上的H與第n+4個氨基酸上的a-羰基O形成氫鍵,使a-helix內(nèi)部的氫鍵數(shù)目達到最大;a-helix只能由L氨基酸或D氨基酸構(gòu)構(gòu)成,天然蛋白的a-helix當然只能由L氨基酸構(gòu)成;L氨基酸既可以形成右手a-helix也可形成左手a-helix,但天然a-helix全部為右手a-helix;影響a-helix穩(wěn)定的因素:相鄰R基團間的靜電作用、范德瓦爾斯作用、疏水相互作用或位阻作用;Pro和Gly;a-helixN-末端和C-末端氨基酸R基團的性質(zhì)Notesfora-helix
M.
F.Perutz(1914-2002)J.C.Kendrew(1917-1997)W.L.Bragg(1890-1971)1962年Nobel化學獎與其父W.H.Bragg獲1915年Nobel物理獎a-helix研究的失敗者獲1954年Nobel化學獎1901-19941897-19711914-1995a-helix研究的成功者liguofuPeptidebondisrigidandplanar1.49?1.27?1.32?WhyandAnswerliguofu
2.
b-pleatedsheetTheaxialdistancebetweentheadjacentaminoacidresiduesis~3.5Angstromsliguofuliguofu
3.
bturnliguofuItoftenconnectstheendsoftwoadjacentsegmentsofanantiparallelb-pleatedsheet.
bturnsareoftenfoundnearthesurfaceofaprotein.TheessenceofthestructureisthehydrogenbondingbetweentheC=OgroupofresiduenandtheNHgroupoftheresiduen+3.GlyandProareoftenfoundinbturns.
3.
bturn(ctnd)liguofuliguofuAA’stendencyinsecondarystructureliguofuRelativeprobabilitiesthatagivenaminoacidwilloccurinthethreecommontypesofsecondarystructure.liguofu§3.3Tertiary&QuaternaryStructureFibrousproteins
areadaptedforastructuralfunctionGlobularproteinsandtheirStructruralpatternsliguofu
-KeratinCollagenSilkfibroin1.
Fibrousproteinsliguofua-keratinsliguofusimpletertiarybutcomplexquaternarystructurea-keratinsliguofua-keratins:Permanentwavingofhairliguofu
a-keratinsRichinhydrophobicresidues:Phe,Ile,Val,Met,andAla.Twoa-helixwrapinparalleltogethertoformacoiledcoilinleft-handedThehydrophobicRgroupsoftwoa-helicesmeshedtogetherinaregularinterlockingpattern.Themaincomponentsofskinandmanyskinderivativesinvertebrateanimals.Usuallyhardera-keratinscontainhighernumberofCys.canbestretched(totwiceasitsoriginallength)duetoitsstructurespringines.liguofuCollagen-chain:auniquesecondarystructureliguofuliguofuliguofu3left-handed-chainwrappedtogethertoformright-handedtriplehelixwithH-bondsininterchaibutnotinIntrachainArepeatingtripeptide:Gly-X-ProorGly-X-Hyp,Gly-Pro-Hypmorefrequent.Glycanfitintothecrowdedinteriorofthetriplehelix,whilePropermitsthesharptwistingofthecollagenhelix.About25%ofthetotalproteinmassinmammalsiscollagen:tendons,cornea,theextracellularmatrixofskinandbonematrix.Collagenfibershavesimilartensilestrengthasasteelwireofequalcrosssection.CollagenliguofuStrandsoffibroin(blue)emergefromthespinneretsofaspiderinthiscolorizedelectronmicrograph.SilkfibroinliguofuliguofuSilkfibroinFibroinisrichinAlaandGly,permittingaclosepackingofsheetsandaninterlockingarrangementsofRgroups.OverallstructureisstabilizedbyextensivehydrogenbondsandbyoptimizationofvanderWaalsinteractionsbetweensheets.Silkdoesnotstretchsinceitsconformationisalreadyhighlyextended.Structureisflexiblesincethemajorforceholdingsheetstogetherisweakinteractionsratherthandisulfidebondsasin–keratins.liguofu2.GlobularproteinsandtheirStructruralpatternsMyoglobinStructruralpatternsliguofu1.Myoglobineight-helices;hydrophobicRgroupsintheinterior;twohistidineintheinterior;polarRgroupsonthesurface;hemegroupinacrevice(pocket);ThefirstproteinwhosestructurewasdeterminedliguofuliguofuDomainMotif/supersecondarystructureStructuralClassQuaternarystructure&symmetry2.StructruralpatternsliguofuTroponin(肌鈣蛋白)C,twoseparatecalcium-bindingregionsWithinalargerpolypeptidechain
Domainsare:
compactregions/distinctstructural
unitsIndependentinthermodynamicstabilityandsometimes,haveseparatefunctions.liguofuMotifs/supersecondarystructuresarePatternsbuiltwitha-helix&/orb-sheetUnitsthatbuildaproteinMotif:模體或模序、基序liguofuliguofuGreekkeyliguofuproteinstructuralclassificationliguofuliguofuliguofuliguofuQuaternarystructures&symmetryliguofuliguofuliguofuHumanpoliovirus(脊髓灰質(zhì)炎病毒)liguofu§3.4
Folding,
Unfolding&RefoldingLossofstructureresultsinlossoffunctionDenaturationofsomeproteinsisreversiblePolypeptidesfoldrapidlybystepwiseprocessDeathbymisfolding:theprion(朊病毒)ProteinfoldinginvivoliguofuLossofstructureresultsinlossoffunctionDenaturant:Destroyhydrophobicinteraction:去垢劑,有機溶劑等DestroyHbondsDestroystaticelectricalforceTemperature尿素、胍鹽、酸、堿liguofuDenaturationofsomeproteinsisreversibleliguofuliguofuPolypeptidesfoldrapidlybystepwiseprocessliguofuliguofuliguofuDeathbymisfolding:thepriondiseases(1)NormalbraintissueSpongybraintissueTransmissibleSpongiformEncephalopathiesAnimalScrapie:羊搔癢病BSE(bovinespongiformencephalopathy)(Madcowdisease)HumanCJD:Creutzfeld-JacobDisease,克雅氏病GSS:Gerstmann-Straussler-Scheinkersyndrome,GSS綜合癥FFI:FatalfamilialInsomnia,致死性家庭失眠癥Kuru:庫魯病AlpersSyndromeliguofuDeathbymisfolding:thepriondiseases(3)1982,StanleyB.Prusinercoinedtheword“prion”referto“proteininfectiousparticle”1997,StanleyB.PrusinerwontheNobelPrizeinPhysiologyorMedicineliguofuDeathbymisfolding:thepriondiseases(4)PrPCPrPSCPrP
=
PrionProteinC
=
CellularSc
=
ScrapiePrPSCfurther
inducesPrPCintoPrPSCliguofuNeed:
Proteindisulfideisomerase(PDI)
Peptidylprolylisomerases(PPIases)Molecularchaperonesareproteinsthatinteractwithpartiallyfoldedorimproperlyfoldedpolypeptides,facilitatingcorrectfoldingpathwaysorprovidingmicroenvironmentsinwhichfoldingcanoccurProteinfoldinginvivowell-studied.Hsp70family:heatshockproteinsGroEL/GroESsystemliguofuProteindisulfideisomerase(PDI)liguofuPeptidylprolylisomerases(PPIases)liguofuDnaK&andDnaJinE.colihomologsoftheeukaryoticHsp70&Hsp40liguofuGroEL/GroESsysteminE.coliliguofuliguofuTheEndliguofuliguofuHbondsBetweenneutralgroupsBetweenpeptidebondsIonicinteractionsAttractionRepulsionvanderWaalsinteractionsAnytwoatomsincloseproximityHydrophobicinteractionsFourTypesofNoncovalent(“Weak”)InteractionsamongBiomoleculesinAqueousSolventliguofu四種作用力強力弱力引力電磁力
離子鍵
共價鍵
金屬鍵
范德瓦爾斯力
氫鍵
疏水相互作用StericforceSolvationforce分子作用力(molecularforce)Intramolecularforce分子間作用力(intermolecularforce)liguofu范德瓦耳斯力(vanderWaalsforce)范德瓦耳斯力偶極靜電力:離子與偶極子間或偶極子與偶極子間的吸引力誘導偶極力:離子或偶極子與其誘導出的偶極子間的吸引力色散力:瞬時偶極子與其誘導出的偶極子間的吸引力liguofuIntermolecularforceliguofu色散力(LondonDispersion)liguofuHydrogenbondliguofuliguofu常見生物分子間的氫鍵角度與氫鍵的強弱liguofu疏水相互作用(Hydrophobicinteraction)Amongtheseforcesthehydrophobic(whichliterallymeans‘water-fearing’)force,hasattractedalotofinterestprimarilybecauseoftworeasons.Firstly,itissignificantlylongerrangedthantheothers;itsinteractionlengthcanbeaslongasabout100nanometerswhereasthatofothersnormallydoesnotexceed5nanometers.Secondly,thereisnosatisfactoryexplanationforitslongrangenature.liguofuΔG=ΔH-TΔS
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