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homogenized
About50mlhomogenizationbuffer
(10mlhomogenizationbufferper2~2.5gtissue)
Washedwithhomogenizationbuffer
Mincedwithscissor
weigh
livers
sacrificed
11C57micewerestarvedfor18to24hours
About1/22liver
Crudenuclear
homogenize
Resuspendedinabout50mlhomogenizationbuffer
15,000g×
15min
50mlhomogenizationbuffer
144,000g×
1hr
cytosol
microsome
5mlhomogenate
45mlhomogenate
Crudemitochondria
(appliedtopurification)
Resuspendedin24ml25%Nycodenzbuffer
12mlhomogenate
52,000g×
90min
5ml34%Nycodenz
8ml30%Nycodenz
12ml25%Nycodenz
8ml23%Nycodenz
3ml20%Nycodenz
AppliedtoNycodenzdensitygradientcentrifugation
Band(30%/25%)
Combinetogether
Dilutedwithhomogenizationbuffertoabout10ml
1mlhomogenate
9mlhomogenate
15,000g×
15min
Purifiedmitochondria
(forsubmitochondrialfraction)
(appliedtosubmitochondrialfraction)
Suspension
0℃20min,gentlestirring
50mlswollenbuffer
0.5MATP(500×
);
1.0MMgCl2(1000×
)
Suspension
35,000g×
20min
0℃5min,gentlestirring
intermembrane
2strokesofatight-fittingpestle
1,900g×
homogenate
mitoplast
Crudeoutmembrane
Alkalibuffer(0.5mg/ml)
Hand-drivenhomogenize
0℃20min
100,000g×
30min
matrix
Crudeinnermembrane
Crudeoutermembrane
Contactsites
(37.7%and51.3%)
Outermembrane
(25.2%and37.7%)
121,000g×
1.2ml25.2%Sucrose
1.2ml37.7%Sucrose
1.2ml51.3%Sucrose
Appliedtosucrosedensitygradientcentrifugation
Hand-drivenPotterhomogenizer
1mlSucrosedilutionbuffer
Mitoplast
(below51.3%)
10VSucrosedilutionbuffer
184,000g×
Outermembrane
Innermembrane
11C57micearestarvedfor18~24hoursandsacrificed.Theliverswereexcisedimmediatelyandrinsedwithice-coldhomogenizationbuffertoremovetheremnantblood.Weightheliversandseparateabout1/22astotalliver.Theremnant21/22weremincedwithscissorsandhomogenized,usingabout50mlhomogenizationbuffer(about10mlhomogenizationbufferper2~2.5gtissue).Thehomogenatewasthenfilteredthroughawiregauzetoremovesomebiggertissue.
Theflow-throughhomogenatewascentrifugatedin1,000gfor10minutes.Thepelletwascrudenuclearandthesupernatantwascentrifugatedagainin1,000gfor10minutes.Thisstepwasrepeatedfor2times.
Thefinalsupernatantwascentrifugatedin15,000gfor15minutes.Thepelletcontainedprimarilymitochondria,andthesupernatantwasagaincentrifugatedin144,000gfor90minutestogetmicrosomepelletandcytosolsupernatant.
Themitochondria-containedpelletwasrinsedwithhomogenizationbufferandcentrifugatedin15,000gfor15minutes.Thisstepwasrepeatedfor2~3timesandthefinalpelletwasresuspendedinabout50mlhomogenizationbuffer.About5mlhomogenatewasseparatedandcentrifugatedin15,000gfor15minutes,andthepelletwasusedascrudemitochondria.Theother45mlhomogenatewascentrifugatedin15,000gfor15minutestooandthepelletwasappliedtofurtherpurification..
ThecrudemitochondrialpelletwaspurifiedfromNycodenzdensitygradientcentrifugation.Thepelletwasresuspendedin24ml25%Nycodenzbuffer.Anddividedintotwoequalpart,12mlforeach,andappliedtotwoseparateddensitygradientcentrifugation.Thegradientwasconsistof5ml34%Nycodenz,8ml30%Nycodenz12ml25%Nycodenz(whichcontainedthesample),8ml23%Nycodenzand3ml20%Nycodenz.Aftercentrifugationin52,000gfor90minutes,thebandintheinterfaceof30%and25%Nycodenzofthetwotubeswascollected,combinedanddiluted15,000gfor15minutes,withthepell