The use of 3-aminophthalimide as a pro-chemiluminescent label in chemiluminescence and fluorescence-based cellular assays.
Demetra Mavri-Damelin, Jonathan Wilden, Ali-Reza Mani, Clare Selden, Humphrey J F Hodgson, Leonard H Damelin
文献索引:Bioconjug. Chem. 20(2) , 266-73, (2009)
全文:HTML全文
摘要
We present a labeling system for direct chemiluminescence-based cellular bioassays using the stable pro-chemiluminescent, luminol precursor, 3-aminophthalimide (API). API-coupled reporter molecules are detected chemiluminometrically after treatment with hydrazine, which converts the API label to luminol. API derivatives containing a variety of functional groups are readily synthesized, allowing for ease of coupling via the imide nitrogen to a host of reporter molecules. The fluorescent nature of APIs further allows for dual fluorescence and chemiluminescence studies. To highlight the utility of this label, we show that API-labeled insulin can be successfully utilized in cellular binding and transport assays and that an API-coupled mitochondrial probe (API-triphenylphosphonium(+)) can be used to both fluorescently and chemiluminometrically investigate mitochondrial function. We also assess the use of API as a polysaccharide and nucleic acid label, and we show that API-labeled palmitic acid undergoes cellular transport and lipid metabolism.
相关化合物
相关文献:
177. Chemiluminescent organic compounds. Part VII. Substituted phthalaz-1: 4-diones. Effect of substituents on the luminescent power. Drew HDK and Garwood RF.
[J. Chem. Soc. , 836-837, (1939)]
A Study of the Aminophthalimidoacetic Acids1. Caswell LR and Atkinson PC.
[J. Org. Chem. 29(11) , 3151-3154, (1964)]