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Chapter 2 The structure of cells(第1页)

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Chapter2Thestructureofcells

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&iccellssharethesamebasiclayout,inthattheyaresurroundedbyamembrane,ahwithinwhichthereisavarietyofmembrane-baperformspecializedtasks.ahenucleuswhisDNA.Atroughlyohousandththevolumeoftheeukaryotee,theanizationofaprokaryoteisrelativelystraightforwardbyparison,althoughbacteriapossessverysimilarstructuralaspedmaerytoeukaryoticcells.Theircellmembrahesamelipidbilayer(illdisext)andtheirmolecularmaerysuesforproteinassemblyfunuchthesamewayaseukaryotes.Bacteriadohavespecializedcellstruotilitysuchasflagella,andmaypossessinternalmembrahecaseofagasvacuolethatservesasabuoyancyaid.However,theDNAinabacterialcellisasinglecircularmoledthereisenuent.

Thecellmembrane

Allcellsareenclosedbyaboundarystructure,theplasmamembrane,whichprovidesabarriertootherdtheexternalehoughthemembraaients,unis(bacluded)usuallyhaveextramaterialosideandplantcellsarecharacterizedbyarigidcellwallofcellulose(Figure4).Overaturyofiionhasshowobeanincrediblypliddynamicmixtureoflipid(fat)moledproteins.Althoughthebasicstructureoftheplasmamembraremelythin-justaoleculesthiingalipidbilayer-itisextremelytoughandflexible,aoallowforthetexoleculesbetweessurroundings.Thisisachievedviathewaterthattlyentersasinaannerbringingsolublemoleculeslikeoxygen(neededasafuel),aissuchasdieexternalmaterialbephysigulfedbythemembrane,aproasphagocytosis.Thereverseprocessisexocytosis,inwhichamembrane-bouerialdestireachesthecellsurface,atwhiembranesfuseahethetswiththerityofthemembrahedynamiatureofthecellmembraneissuchthattheentireplasmamembraurnedover’(replahourlybasis.

&heearliestexperimentsinvolviionsoflipidsaoexplaiiesofmembraneswereperformedtowardstheehtury,oableinGermanybyAgnesPoesstudiedthebehaviourofoilpouredontowaterinaflatdish,identifyingtheinfluenpuritiesonthesurfaoffluids.Sheseh,whowassuffitlyimpressedtogetthempublishediifialNaturein1891.In1932,IrvingLangmuir,winNewYork,rizefthatlipidsspreadonroducealayeronlyohidthatallthemoleculeswereoriehesameway.Thishappensbeeendofthelipidmoleculeisattractedtowater(itishydrophilidtheothereishydrophobic).Eachlipidmoleculeisshapedlikeanold-fashiohespeg,withthetopofthepegbeingthehydrophilidthetwolegsofthepegrepresentingthehydrion.Allthepegsfloatonthesurfaceofwaterheaddown,legsuppermamonolayer.IerandJamesGreedmembranesfromredblooddingthatmembraneoftwolayers(abilayer)oflipids,makingasandwichwiththehydrophilicpegheadsosides,andthehydrophobitheihereiswaterbothisidethecell,thisarraismaintaihhydrophetherontheihemembrahisarrawasdirectlyvisualizeddecadeslaterwiththeadveronmicroscopy,wherethihighmagnifibrawodarkliedbyalightregiohem(see,forexample, Figures 4and141935,JamesDanielliandHughDavsohislipidbilayerwasbothsidesbyalayerofproteilasteduntil1972whenSeymarthNisuggestedthattheproteinscouldalsobethreadedthroughthelipidlayers,afromeithersideofthemembrahthisfiguratioraeins,andasiweaveitswaythroughthelipidbilayerseveraltimes.Thelipidmoleamembranearehighlymobile,tlymovingpastohemembraeiothedesofthe‘fluidmosaie.ThisactivityofthelipidswasedbyMichaelEdidinin1970,whehemembranelipidsoftwodiffereypeswitheithergreenorredfluorestchemicals.Thisgavea‘patchwreenlabellingfromindividualcellsgrowherinamixedcellculture.Edidinthenaddedvirusestotheculturewhichcausedthemembranesofadjatcellstofusetoeachother,thusmixingtheirmembranelipidsand,withinanhreenpatchesoffluorescewerereplaelabelling,showiemixingoftheindividuallylabelledlipidmoleculeswithinthefusedmembranes.

&hroughaplantcell,showingthemaindifferenalcells:acellwalloutsidethecellmembrane,chloroplastswithstars(SG)ihem,andalargevathetreofthecell

Withinthisotionofthelipids,groupsofmembraarouhelipidbilayerratherlikeicefloesinthepolarseas.Sometimesafewlipidmoleculeswillformaclusterforafewsedsgspecializedareascalledmembras.Membrasweredislyredtheirfunotyetpletelyuood,althoughitseemslikelytheyareinvolvedinsigweeherearearound500differentmembranelipidswhidandanchordiffereelsthroughthemembraroltheuousflowofmoleculesacrossit.

Theseelsenableaomaintainaninterionofsodiumthatisoheexterion.Thisrequirestpumpingtoremovesodiumwhichotherwisewouldraisetheosmoticpressureinthecellwhiturn,ater,withthepotentialtoburstthecell.Atthesametime,potassiumismaihiamuchhighertratioerhesamemembranepumpbringspotassiumieassodiumispumpedout,anactivitythattakesaboutohirdofthetyofthecell.

Proteihesurfabraasreceptnallingmoleoutsidethecell.Thesemessagesarethenpasseddoweinswithiheoswites,ifrequired,ieredonessusulinwillidirectlywiththemembrane,alloassiuallyeverythingthatgoesoherinfluences,orisinflflflueheabras500typesoflipidmoledupto10,000typesofmembraeins.Cells‘feel’theirimmediatesurroundingswithfififiensionscalledmicrovilli(seeFigure3a–eepithelialcellssuchasthoseresporieheguts,themembranebeesfashiooabrushborder,wheretightlypackedmicrovilliihesurfacearea30-fold(seeFigure14inChapter5).Whileitisimpossibletoprioritizevariouspartsofthecell,astheyaremutuallyi,withoutmembralifeotexist.

Membranesinsidecells

Membranesarealsocruciallyimportantiworeasons:first,toprovidesurfawhichchemicalreaprodsedlytoprovideseparateareasiheicalreastoproceedwhichmightotherwiseiheachother.Iheinnersurfaceoftheplasmamembrahepositiwithinthedprovidesattatpointsforintracellulartsthatobeinspecifis.Usingtheanalogyofthecellasafactory,theinternalmembranesprovidetheworkbenches,floors,gs,andwallsforallthedifferentpartsofcellprodu,withtherallypositioheoffiwhiformationisstored.Insmallcells,suchasbacteria,whichareusuallyrodshaped,theiheplasmamembraneprovidesalargesurfarelatioerior,sothatanythingthatneedsafixedpositionbe‘hung’ontheinside,alybadotherprenerallyhavelittleornointernalmembraioheinternalvolumeofeukaryotecellsisathousaofabacterium,sothattheeukaryoticcellrequiresavastinternalmembraemaroundahuheareaoftheplasmamembrahisiionofbiochemicalactivitiesiscrucialastherearehundredsofchemicalreasgoingonthatseriouslyiheachother.Prokaryotes,withnointernalmembraestosomeextehisproblembyaggregatinggroupsofspezymesintomultiproteinplexes,whichworkasfreeentitiesiheadditioesediffereabolicprocesseswithinmembraments.Themajorinternalmembraemiiccellsistheendoplasmicreticulum(usuallyshorteoER),whisahroughouttheehispartofthecelliscalledthe(everythihecellmembraneexgthenucleus;Figure5a,b)ahinginitissurrouheplexmixtureofsubstancesdissolvedinwater,likeaveryolecularsoup’.

5.Internalcellmembraructures.(a)Thenuvelope

&esthehe,whisanellesingmito)andendoplasmicreticulum(ER).(b)Amitosurroundedbyspiralpolyribosomes(r)attachedtothesurfaceoftheER.(uplex,elarrowed.(d)Golgibodies(Go)prisedofstabranes

anelles

Twaheitodriaand,inplants,chloroplasts—havedouble,ratherthansinglemembrahisismostlikelyahangoverfromwhentheywerefree-livingformsearlyincellularevolutioheywereiercell,theirownmembranebecamesurrouhecellmembra.BothmitodriaandchloroplastsA,furtherevideheywere.Therearetwotheoriesastohowchloroplastsandmitodriabecamepartofeukaryoticcells:theycouldhave‘iheeukaryotecellor,alternatively,beenengulfedbyalargeriionshipinwhichbothpart.

&iccellprovideda‘safe’e,inwhichthemitehatcouldbeharvestedbythehostd,inplantcells,chlorlucosebyphotosynthesis.Inmityisprlucosebyaprocesscalledoxidativephosphorylation,whichothesurfaternalmembraae(Figure5b).Inchloroplasts,glucoseisproducedbyphotosyizymesinstabrahylakoids(Figure4).

Allothermembrane-banelles(colleownasvacuolesorvesicles)haveasinglebilayermembraypicalcellwillhavearound1000ofthesevadasimilarodria.Secretoryvesitainchemigerssuonesforreleasefromthees,lysosomes,andperoxisomes(seeFigure2)allvariousmixturesofeeinsthatcatalysechemicalreas.Lysosomesbelikeomachofthecell,astheyhydrolytizymesthatbreakdownbiologicalmaterialintoitstpartstoprovidefoodfortheesalsofusewithphagocyticvacuoles(phagotainierialsuchasbacteria,killingaheinvadinganisms.TheBelgiadeDuvediscoveredlysosomes,forwhichhereceivedtheNobelPrizein1974.Healsodiscoveredperoxisomes,whichreplicatebydivisioodriaandchloroplasts,butdoheiroeroxisomesareinvolvediyofbiochemicalpathwaysandatleast50differeheyareimportantinthebreakdown(oxidation)ofsubstancessuchasfats,providingamajorsouretabyina,andplantcells.Beeoftheproductsofoxidatienperoxide,whichisharmfultotheesalsoenzymecalledcatalase,whichbreaksdownthehydrogeer.

Peroxisomesarealsositesofsynthesisofseveralehoseinlivergrespoheproduofbile.Aswithmostindividualaionsinperoxisomeformationhaveseveredaingwillusuallyleadtoafertilizedeggfailiafewdivisions.

&eofproteinproduforthetsofthevariousvacuolessuesandperoxisomesisatthemembraheERwasdiscoveredbythreepioronmicroscopy—KeithPeePaladeinNewYorkandFritiofSjostraheearly1950s.Eleicroscopyallowsa1000-foldiailparedtoallightmicroscopy,butimposesdiffithepreparationofspethataronbeamlypassthroughextremelythiiohediffieioronmicroscopy,Porterandhiscolleaguesopeureinareviouslyunimagiroke,indistindirregularshadowylumpsfromlightmicroscopywerevielydistinellessuchasmiture 5b).InthewordsofDo,acolleagueofPorterandPalade,‘fists,thede1950to1960heldthesameantiaattendstheopeniiioatlasesofbiologicalultrastruaillclassicstothisday.

&hecell

MitodriawerefirstisolatedbiochemidanalysedbyAlfredLehningerin1949,ingthepreseheenzymesrequiredfeionbyoxidativephosphorylation,ahighlyeffitprowhitsareoxidizedtoproduosiriphosphate(ATP).Theenergyfwork,buildingproteinsandmovingthingsarouoredinamoleculeofATP.TheePisstoredin‘highenergy’phosphatebonds.Tovolvedbiochemicalprocessshort,thisehereleaseofelethecitricacidcythemitoembraingATPsynthase,aheP.EnergyisreleasedfromATPwheebondsarehydrolysed(aprocesswherethemoleculeissplitintotwopartsbytheadditionofamoleculeofwater).Withthereleasey,ATPisvertedtoADP(adenosinediphosphate)whituredbacktoATP,staiherelease.

OnlythreeyearsafterLehninger’sbiochemicalcharaitodria,Palade’seleicrographsshmembraure(Figure 5b).Theorderofthesediscoveriesrefieoveralltrendthatthe‘grindandfind’wsofbiochemistryhaveofteedseminalinformationosiheiractualimagironmicroscope,althoughinthemicroscopist’sview,nothingparewithseeingwhatthetsofthecelllooklike.Thedifferentapproachesofthebiodbiologistbeillustratedasfollows.Presumeherhadeverseenawristwatch,butresehation.Afewdayslaterthebiochemistwouldreportthatthewatchhadbeenanalysedbyseparatingit(grindingitup)intoitspos.Thisanalysiswouldshowthatthewatchwasmadefromvariousproportionsofcopper,brass,steel,ahmaybeafewdiamonds.Thebiologistwouldhatagdohahebadreportthatitseemedtohwhichpoweredaseriescogwheels,thatdrovetwoarmsoofthewatchthatseemedtorotateatatspeed.Whilemassivelyoversimplified,thisparisongivesahediffereheanalyticalapproachofthebiodtheobservationalapproachofthebiologist.Fortunately,usedtogether,thesehavebeenfruitfulindeedincellbiology.

Proteinprodu

&otheER,themajorityofERmembranesarecoveredwithribosomes(Figure 5a)andareknhER,whilsttheremainderbearnoribosomes(smoothER).Thejobofribosomesistomake(syeinsfromaminoacids,holdingandjoiningtheaminoaakepeptides,theidesaeins.AseriesofRNAmoleculesareieinsynthesis.IhehesequenucleotidebasesfthecodeforaparticularproteinisfirstplateDNAinaprocesscalledtrans,produewmoleessengerRNA(mRNA).Messeheofthenudergoingmodifi(calledspligtheway.Ooplasm,ribosomesbindtomessengerRNA,whiactsasatemplatefortheliherofaminoatoproteins,aprocesscalledtranslation.

TheaminhttotheribosomebyshortRNAmoleownastransferRNA.ProteiheERehespa)betweentheERmembranes(Figure 5b),wheretheyarefoldedintoafinalfiguratipassedoessuchastheGolgibodies(Figure 5d).TheGolgibiapparatus)isastackoffiattenedmembranevesicles,whereeinsarepatovacuolesfordistributihoutthedmayalsohavesugarsaddedinaproasgly.hesizedproteiriyd,shouldtheybedefeanyway,theyaretaggedbymoleculesofubiquitinforsroteinmisfoldirimeodisorderssuchascysticfibrosisaeinqualityeismsmaybeelesseffectiveaswegettoAlzheimer’sdiseaseande-relatedives.

&hesizedandfolded,eioreachtheirfiionwithinthegsttheotherbillionsofproteiahesizedanddegraded.Someproteihowomembranebarriersbefthesitewheretheyfulflltheirfun1971,GünterBlobelandDavidSabatinifromtheRockerfellerInstituteinNewYesteda‘signalhypothesis’,inwhisweregivenaluggagelabel,orzipcode,toeheyfiherightdestinatioakestheformofshortsequeninoaoogenials,whiattachtoreceptorproteinstoallowthemthroughmembraoreachthecorreation.In1999,GünterBlobelreceivedtheNobelPrizeforthiswork,laihemolecularmeismsbehindseveraldiseases.Bothcysticfibrosisandprimaryhyperoxaluria(agkidanearlyage)arecausedbyproteinsfailiheircorreatioedthemilliondollarprizemo-warrestruDresdehetryofhisbirth.

Lipidprodu

&sroleihesis,theERisaversatileanellewhibothredtransmitsignalsandactasacellularstoreforcaldisalsorespohesynthesisoflipids.Withinindividualcells,fatisproducedatthesurfaceoftheERastinyindividualdroplets(lipogehoughfatthatwearefamiliarwitharoundtheedgeofoursteaksandoftenaroundourwaistliobeinsolidhomogenouslumps,itallexistswithinmembrane-boundfatdropletsinindividualcellstermedadipocytes(seeFigure3d).Givenauousirients,adipocyteswillaccumulatemoreandmorelipiddroplets,whichcoalescewiththeirneighbourstobeelargerandlarger,agforthevastmajorityofthee,whireaes‘normal’size.Obesityistlyadisybalaresultsfromtheuedacoflipiddropletswithies.AtthispoiregrettheefficyoftheER,besidesprovidingforfatste,theERalsosynthesizesehesmoothERtobreakdorocesstermedintracellularlipidhydrolysisorlipolysis.Thus,amajorfabodyweightisthebalahesynthesisandbreakdownoflipidsintheER.gthehealthcesofbeiissurprisingthatfatatthecellularlevelhasreceivedrelativelylittleattention,withlipiddropletsthoughtofashaedepots.However,udiesareshowianelles,andanythingbut‘lumpsoffat’.Alleukaryoticcellshavetheabilitytomakelipids,whichproduceallthenaturallyoilsandfats—fromrapeseedandoliveoiliomilkfats,lanolin,andlardinanimalcells.LipidmoleculesaretratedatthesurfaceoftheER,thenpiningadroplet(uniquelysurroundedbyasinglelipidmonolayermembrane)andremaiheER,wheretheecatalyselipidsynthesisarelocated.Mitodriaarecloselyassociatedwiththesitesoflipidprodu,providingtheenergyforfatformatioodriaareactuallytetheredtothesurfaceroupofmembraeins.Asmorelipidisaccumulated,individualdropletsfusewiththeirneighbwhichtheseparatemembraiallyprodugeverlargerdroplets(Figure3d).Durihisprocessisreversed.Bigdrmeosmallerones,andenzymesfromsmoothERbreakdownthelipidmoleculesthatprhthemembrahesizeofthedropletfromtheoutsidein>

&ionoflipidsalsoocthedintheliningofbloodvessels,particularlyththewallsofmajorarteries.Hereacoflipidsleadstoformationoffattyplaques,resultinginatherosclerofthearteries),whichlimitsbloodflowandthusleadtoheartattadstrokes.Atothersites,iionofbloodflorodueyfailurerene.Excessiveacoflipidsisalsoamajorfatypetwodiabetesaeatosis(fattyliver).Exptionofalgesitheliverbreaksdownas,leadingtomoreseveressuchascirrhosis.Fortuhefatdropletsstillbebrokendowniheisreversiblewithreduptionofalcohol.Allthisbadhereasoioherwemightteroffwithoutfatcells,buttheyfunrespoionarypressures,allowingfethatmayedussurviveintimese,andalsoallowingmanyothermammalstosurviveseverewintersbyhibernation.

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