A new peptidic vector for molecular imaging of apoptosis, identified by phage display technology

被引:47
作者
Laumonier, Catherine
Segers, Jerome
Laurent, Sophie
Michel, Alain
Coppee, Frederique
Belayew, Alexandra
Elst, Luce Vander
Muller, Robert N.
机构
[1] Univ Mons, Dept Gen Organ & Biomed Chem, NMR & Mol Imaging Lab, B-7000 Mons, Belgium
[2] Univ Mons, Lab Prote & Prot Chem, B-7000 Mons, Belgium
[3] Univ Mons, Mol Biol Lab, B-7000 Mons, Belgium
关键词
phage display; apoptosis; phosphatidylserine; MRI; contrast agent;
D O I
10.1177/1087057106288220
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phosphatidylserine (PS) exposure on the cell surface is an early marker of apoptosis. To select PS binding peptides as vectors of contrast agents to image apoptosis, a phage library has been exposed to perfused mouse livers. Phages not retained on control livers during the first perfusions were used for selections on apoptotic livers in a second series of perfusions. Four selected phages were further evaluated for binding to PS-coated enzyme-linked immunosorbent assay (ELISA) plates. They presented an apparent affinity constant (Ka (app)) for PS ranging from 6.08 x 10(10) M to 1.62 x 10(11) M. These phages did not bind to phosphatidylcholine, and competition with annexin V confirmed their specific interaction with PS. The phage with the highest affinity-bound PS in ELISA with a Ka (app) = (1.6 +/- 0.2) x 10(11) M. It carried the TLVSSL peptide that was synthesized. Specific competition with annexin V and with the synthetic peptide was performed and confirms the specificity of the interaction.
引用
收藏
页码:537 / 545
页数:9
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