Real time detection of cell cycle regulator cyclin A on living tumor cells with europium emission

摘要

Six water-soluble europium complexes (Eu-L_1-P_n and Eu-L_2-P_n, n = 1, 2 and 3) with one antenna chromophore, two different linkers (L_1 and L_2) and three proposed cyclin A specific peptides (P_1: -GAKRRLIF-NH_2; P_ 2: -GGAKRRLIF-NH_2; P_3: -Hex- GAKRRLIF-NH_ 2) have been synthesized. With structural information available, comparisons of the cyclin grooves of cyclin A and the six europium complexes have been made, and insights have been gained into the determinants for peptide binding and the foundation of differential binding. Experiment-wise, the linear and two-photon induced photophysical properties of these conjugates were monitored in aqueous solution. Numerous in situ/in vitro biological assays have been carried out, such as responsive emission changes in situ/in vitro, Western blot and cellular uptake. As imaging agents, complexes with peptides P_ 3: -Hex-GAKRRLIF-NH_2 showed high selectivity to cyclin A in numerous cancer cells. When it comes to responsive optical signal changes, complex Eu-L_2-P_3 exhibited a threefold emission enhancement upon binding with cyclin A (100 nM cyclin A, φ = 8% to 21%, log K_B = 5.83, detection limit = 5 nM), and this could be initiated by the shortened distance between the antenna and the lanthanide after they bind/get into cyclin A. It is promising that our compounds (especially compound Eu-L_2-P_3) could serve as the template for structure-guided efforts to develop potential imaging therapeutics on the basis of selective imaging of CDK2/cyclin A activity.