Amino Acid Imprinted UiO-66s for Highly Recognized Adsorption of Small Angiotensin-Converting-Enzyme-Inhibitory Peptides.
Long LiuZhiwei QiaoXinfang CuiChunjiao PangHong LiangPeng XieXuan LuoZuqiang HuangYanjuan ZhangZhongxing ZhaoPublished in: ACS applied materials & interfaces (2019)
Introduction of targeted defects into microporous UiO-66s for manipulating their three-dimensional size and surface properties can endow them with adsorption and separation areas involving angiotensin-converting-enzyme-inhibitory (ACE-inhibitory) peptides. Three hydrophobic amino acids (AAs) (i.e., proline (Pro), phenylalanine (Phe), and tryptophan (Trp)) having different physical/chemical properties were applied to in situ tailor defects in UiO-66 through targeted incoordination of missing linkers or missing nodes. Characterization results revealed a uniform oval shape of the developed defects with lengths ranging from 1.8 to 3.1 nm, which was also highly consistent with our molecular simulation. Among these three defective UiO-66s, Phe and Trp imprinted UiO-66s significantly promoted the adsorption affinity of small ACE-inhibitory peptides (uptake: 1.25 mmol g-1 for DDFF and 1.37 mmol g-1 for DDWW) and ultrahigh selectivity for DDFF (249) or DDWW (279) from inactive KKKK solution based on a lock-and-key mechanism. As a result, the imprinted UiO-66 showed an enrichment capacity for ACE-inhibitory peptides about eight times higher than that of pristine UiO-66. Therefore, the amino acid imprinting strategy endorsed by its facile and discerning ability can be envisioned to be of great value for small functional peptide separation and oriented enrichment in biomedicines.
Keyphrases
- angiotensin converting enzyme
- amino acid
- metal organic framework
- angiotensin ii
- aqueous solution
- cancer therapy
- squamous cell carcinoma
- photodynamic therapy
- early stage
- single cell
- liquid chromatography
- sentinel lymph node
- drug delivery
- solid phase extraction
- radiation therapy
- single molecule
- rectal cancer
- mass spectrometry
- capillary electrophoresis
- tandem mass spectrometry
- simultaneous determination