BAK/BAX activation and cytochrome c release assays using isolated mitochondria
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作者:
Renault, Thibaud T.
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Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
Dept Dermatol, New York, NY 10029 USA
Tisch Canc Inst, New York, NY 10029 USA
Metab Inst, New York, NY 10029 USAIcahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
Renault, Thibaud T.
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Floros, Konstantinos V.
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Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
Tisch Canc Inst, New York, NY 10029 USAIcahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
Floros, Konstantinos V.
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Chipuk, Jerry E.
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Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
Dept Dermatol, New York, NY 10029 USA
Tisch Canc Inst, New York, NY 10029 USA
Grad Sch Biomed Sci, New York, NY 10029 USA
Metab Inst, New York, NY 10029 USAIcahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
Chipuk, Jerry E.
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机构:
[1] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
The mitochondrial pathway of apoptosis proceeds when the outer mitochondrial membrane (OMM) is compromised by the pro-apoptotic BCL-2 family members, BAK and BAX. Once activated, BAK and BAX form proteolipid pores in the OMM leading to mitochondrial outer membrane permeabilization (MOMP), and the release of inner membrane space proteins, such as cytochrome c, which promotes caspase activation. The use of isolated mitochondria has been instrumental to understanding the key interactions necessary to engage BAK and BAX activation, MOMP, and apoptosis. Furthermore, it is possible to biochemically define the relationships between BCL-2 family function and mitochondrial physiology using isolated systems. Our laboratory uses freshly isolated mitochondria from numerous sources to better understand BCL-2 family function and requirements for BAK and BAX activation. Here, we will discuss commonly used in vitro techniques to perform MOMP and cytochrome c release assays; and provide several key methodologies to implicate BAK and BAX activity in these processes. (C) 2013 Elsevier Inc. All rights reserved.
机构:
Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, AustraliaRoyal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Ferrer, Pedro Eitz
Frederick, Paul
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Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, AustraliaRoyal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Frederick, Paul
Gulbis, Jacqueline M.
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Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Univ Melbourne, Dept Med Biol, Parkville, Vic 3052, AustraliaRoyal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Gulbis, Jacqueline M.
Dewson, Grant
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Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Univ Melbourne, Dept Med Biol, Parkville, Vic 3052, AustraliaRoyal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Dewson, Grant
Kluck, Ruth M.
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Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
Univ Melbourne, Dept Med Biol, Parkville, Vic 3052, AustraliaRoyal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
机构:
Natl Inst Biol Sci, Beijing 102206, Peoples R China
Peking Union Med Coll, Grad Sch, Beijing 100730, Peoples R China
Chinese Acad Med Sci, Beijing 100730, Peoples R ChinaNatl Inst Biol Sci, Beijing 102206, Peoples R China
Jiang, Xian
Jiang, Hui
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Natl Inst Biol Sci, Beijing 102206, Peoples R ChinaNatl Inst Biol Sci, Beijing 102206, Peoples R China
Jiang, Hui
Shen, Zhirong
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Natl Inst Biol Sci, Beijing 102206, Peoples R ChinaNatl Inst Biol Sci, Beijing 102206, Peoples R China
Shen, Zhirong
Wang, Xiaodong
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机构:
Natl Inst Biol Sci, Beijing 102206, Peoples R China
Peking Union Med Coll, Grad Sch, Beijing 100730, Peoples R China
Chinese Acad Med Sci, Beijing 100730, Peoples R ChinaNatl Inst Biol Sci, Beijing 102206, Peoples R China