Rhodamine 110-linked amino acids and peptides as substrates to measure caspase activity upon apoptosis induction in intact cells

被引:107
作者
Hug, H
Los, M
Hirt, W
Debatin, KM
机构
[1] Univ Ulm, Kinderklin, Forschungslabore, D-89075 Ulm, Germany
[2] Univ Munster, D-48149 Munster, Germany
[3] Orpegen Pharma, D-69115 Heidelberg, Germany
关键词
D O I
10.1021/bi9913395
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Caspases (cysteine aspartate-specific proteases) are a structurally related group of cysteine proteases that cleave peptide bonds following specific recognition sequences. They play a central role in activating apoptosis of vertebrate cells. To measure apoptosis induced by various stimuli and at an early apoptotic stage, caspases are an ideal target. This is especially the case when apoptotic cells have to be analyzed ex vivo before phagocytes remove them. A new and sensitive caspase assay is based on a substrate that contains only aspartate residues linked to rhodamine 110. With this and similar substrates, we are able to detect intracellular caspase activation by flow cytometry after apoptosis induction in intact hematopoetic cell lines.
引用
收藏
页码:13906 / 13911
页数:6
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