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A Small Molecule that Induces Intrinsic Pathway Apoptosis with Unparalleled Speed
Author(s) -
Rahul Palchaudhuri,
Michael J. Lambrecht,
Rachel C. Botham,
Kathryn C. Partlow,
Tjakko J. van Ham,
Karson S. Putt,
L.T. Nguyen,
Seok-Ho Kim,
Randall T. Peterson,
Timothy M. Fan,
Paul J. Hergenrother
Publication year - 2015
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2015.10.042
Subject(s) - apoptosis , microbiology and biotechnology , small molecule , biology , chemistry , genetics
Apoptosis is generally believed to be a process that requires several hours, in contrast to non-programmed forms of cell death that can occur in minutes. Our findings challenge the time-consuming nature of apoptosis as we describe the discovery and characterization of a small molecule, named Raptinal, which initiates intrinsic pathway caspase-dependent apoptosis within minutes in multiple cell lines. Comparison to a mechanistically diverse panel of apoptotic stimuli reveals that Raptinal-induced apoptosis proceeds with unparalleled speed. The rapid phenotype enabled identification of the critical roles of mitochondrial voltage-dependent anion channel function, mitochondrial membrane potential/coupled respiration, and mitochondrial complex I, III, and IV function for apoptosis induction. Use of Raptinal in whole organisms demonstrates its utility for studying apoptosis in vivo for a variety of applications. Overall, rapid inducers of apoptosis are powerful tools that will be used in a variety of settings to generate further insight into the apoptotic machinery.

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