Oriented assembly of hydrophilic nanochains modified by porous zirconium-based coordination polymers for glycopeptides analysis.

Talanta

Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, People's Republic of China; Research Center of Analysis and Test, East China University of Science and Technology, Shanghai, 200237, People's Republic of China. Electronic address:

Published: January 2024

Mass spectrometry (MS)-based glycoproteomics research requires additional sample pretreatment to improve the effective identification of low-abundance glycopeptides without interference from non-glycoproteins. Herein, an attractive strategy using resorcinol-formaldehyde (RF) resin and zirconium-based coordination polymer (Zr-BCP) was established to prepare one-dimensional porous coordination polymer composites for glycopeptide enrichment before MS analysis. The obtained FeO@RF@Zr-BCP nanochains feature excellent magnetic response (42.26 emu/g), high hydrophilicity (16.0°), and large specific surface area (140.84 m/g), which provides abundant affinity sites for specific capture of glycopeptides. The materials exhibit outstanding performance in the enrichment of glycopeptides in terms of sensitivity (15 fmol/μL IgG), selectivity (1:200, molar ratio of IgG/BSA), loading capacity (200 mg/g) and recovery (106.4 ± 3.5%). In addition, the developed method based on FeO@RF@Zr-BCP has been successfully applied to capture glycopeptides in tryptic digest of mouse teratoma cell extracts. It is worth emphasizing that compared with dispersed nanoparticles, the one-dimensional chain structure brings extraordinary reusability to FeO@RF@Zr-BCP nanochains, which is conducive to the rapid cyclic enrichment of glycopeptides. This present work provides a potential enrichment platform for comprehensive glycoprotein analysis, and opens a new avenue for the application of oriented-assembly nanochains.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.talanta.2023.125165DOI Listing

Publication Analysis

Top Keywords

zirconium-based coordination
8
coordination polymer
8
feo@rf@zr-bcp nanochains
8
capture glycopeptides
8
enrichment glycopeptides
8
glycopeptides
6
oriented assembly
4
assembly hydrophilic
4
nanochains
4
hydrophilic nanochains
4

Similar Publications

Harnessing Infinite Coordination Polymers to Eliminate Harmful Environmental DNA for Water Purification.

Anal Chem

March 2025

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, P. R. China.

Harmful environmental DNA (eDNA) contamination in water poses significant health risks, yet traditional treatments fall short of achieving efficient removal. Here, we introduce 1MIA-Zr, a bioinspired infinite coordination polymer catalyst modeled after natural nucleases. 1MIA-Zr achieves a DNA hydrolysis rate approximately 40 times greater than that of UiO-66 REO, the previous best zirconium-based catalyst.

View Article and Find Full Text PDF

Herein, by engineering the geometries of the organic linkers, two pyrrolo-pyrrole-based low-symmetry tetracarboxylate linkers (TAPPs) were successfully designed and subsequently used for the construction of two new zirconium-based metal-organic frameworks (Zr-MOFs) ( and ). The reduction of the linker symmetry arises from both the asymmetric pyrrolo-pyrrole core and the integration of both the - and -benzoate coordination groups on the linkers. Both MOFs are composed of 8-connected Zr nodes and 4-connected highly deformed TAPP linkers with the same topology, but distinct linker arrangements can be observed in two structures.

View Article and Find Full Text PDF

Functional metal organic framework mediated G-quadruplex DNA nanostructures for improved self-powered smartphone-assisted dual-mode biosensing.

Biosens Bioelectron

February 2025

Education Department of Guangxi Zhuang Autonomous Region, Laboratory of Optic-electric Chemo/Biosensing and Molecular Recognition, Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products, Guangxi Key Laboratory of Chemistry and Engineering of Forest Products, Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission, School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning, 530006, China. Electronic address:

Accurate detection of major disease biomarkers is frequently hindered by complex environmental factors and their inherently low expression levels. To overcome these challenges, a self-powered, smartphone-assisted dual-mode biosensing platform has been developed, utilizing functional metal-organic frameworks (MOFs) and G-quadruplex (G-4s) DNA nanostructures to significantly amplify signal output and enhance detection accuracy. This innovative system utilizes gold nanoparticle/zirconium-based MOF/graphdiyne composites (AuNPs/Zr-MOF/GDY) and self-assembles methylene blue (MB) with G-quadruplex (G-4s) DNA nanostructures for detecting the thalassemia gene CD122.

View Article and Find Full Text PDF

Characterization of metal centers in metal-organic frameworks (MOFs) is critical for rational design and further understanding of structure-property relationships. The short-range structure about Zr atoms is challenging to properly elucidate in many Zr MOFs, particularly when local disorder is present. Static Zr solid-state NMR spectra of the seven zirconium MOFs UiO-66, UiO-66-NH, UiO-67, MOF-801, MOF-808, DUT-68 and DUT-69 have been acquired at high magnetic fields of 35.

View Article and Find Full Text PDF

Abnormal kinase expression affects phosphorylation in the human body, which is associated with numerous diseases, including cancer, diabetes mellitus, and Alzheimer's disease. In this study, we synthesized a highly stable, two-dimensional, luminescence-functionalized metal-organic framework with remarkable electrochemiluminescence (ECL) by immobilizing 9,10-Di(p-carboxyphenyl) anthracene (dca) on a zirconium cluster (dca-Zr₁₂) via a strong coordination bond between -COO⁻ and Zr⁴⁺. This novel and simple platform relies on the highly specific identification of phosphate molecules by the ultra-thin dca-Zr₁₂ nanoplate through carboxylate-Zr⁴⁺-phosphate chemistry.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!