Probing the serum albumin binding site of fenamates and photochemical protein labeling with a fluorescent dye.
Tao DengJing ZhaoDanfeng PengXin-Qian HeXin-An HuangChaozhan LinChenchen ZhuLei WangFang LiuPublished in: Organic & biomolecular chemistry (2022)
Human serum albumin (HSA) can bind with numerous drugs, leading to a significant influence on drug pharmacokinetics as well as undesirable drug-drug interactions due to competitive binding. Probing the HSA drug binding site thus offers great opportunities to reveal drug-HSA binding profiles. In the present study, a fluorescent probe ( E )-4-(2-(5-(4-(diphenylamino)phenyl)thiophen-2-yl)vinyl)-1-propylpyridin-1-ium (TTPy) has been prepared, which exhibits enhancement of deep-red to near-infrared (NIR) fluorescence upon HSA binding. The competitive binding assay indicated that TTPy can target the HSA binding site of fenamates, a group of non-steroidal anti-inflammatory drugs (NSAIDs), with moderate binding affinity (1.95 × 10 6 M -1 at 303 K). More interestingly, TTPy enables fluorescent labeling of HSA upon visible light irradiation. This study provides promising ways for HSA drug binding site identification and photochemical protein labeling.
Keyphrases
- anti inflammatory drugs
- fluorescent probe
- living cells
- binding protein
- dna binding
- drug induced
- single molecule
- visible light
- quantum dots
- emergency department
- molecular dynamics simulations
- photodynamic therapy
- transcription factor
- high throughput
- radiation therapy
- high intensity
- drug delivery
- small molecule
- protein protein
- single cell