Literature DB >> 35697330

Probing the serum albumin binding site of fenamates and photochemical protein labeling with a fluorescent dye.

Tao Deng1,2, Jing Zhao1, Danfeng Peng1, Xinqian He1, Xin-An Huang1,2, Chaozhan Lin3, Chenchen Zhu3, Lei Wang4, Fang Liu3.   

Abstract

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 × 106 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.

Entities:  

Mesh:

Substances:

Year:  2022        PMID: 35697330     DOI: 10.1039/d2ob00717g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Using Human Serum Albumin Binding Affinities as a Proactive Strategy to Affect the Pharmacodynamics and Pharmacokinetics of Preclinical Drug Candidates.

Authors:  Jianwei Fan; Katherine Gilmartin; Steven Octaviano; Francisca Villar; Brianna Remache; John Regan
Journal:  ACS Pharmacol Transl Sci       Date:  2022-08-16
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.