Porphyrinic Metal–Organic Frameworks with Longitudinal Pt Deposition Referenced as Opto/Catalytic Adjuvants for Dual-Path Glycoprotein Assay

In this work, porphyrinic metal-organic frameworks (MOFs) with longitudinal Pt deposition were developed for the inspired establishment of opto/catalytic adjuvants referenced for a dual-path glycoprotein assay. In the compositional cooperation, porphyrinic MOFs were synthesized through Zr oxoclusters and polytopic porphyrin ligands into a benchmark template (PCN-222), followed by catalytic Pt nanowire deposition (Pt<sup>NW</sup>@PCN-222). As for signal reflection, the fluorogenic species (i.e., resazurin and amplex red) were integrated into zeolitic imidazolate framework-8 (ZIF-8) via epitaxial shell growth to guide lectin integration. The specific performance toward glycoprotein recognition was guaranteed by both antibody-antigen interaction as well as glycan epitope binding through lectin affinity, and the signal response was initiated by textural decomposition of the ZIF-8 skeleton in a controllable manner. On one hand, Pt<sup>NW</sup>@PCN-222 can function as the catalytic adjuvant to exert the fluorogenic reactions: a reductive <i>N</i>-deoxygenation of resazurin and an oxidative <i>N</i>-deacetylation of amplex red, in which both the redox reactions generated the fluorescent species of resorufin products. On the other hand, Pt<sup>NW</sup>@PCN-222 with endogenous periodical arrangement of porphyrin ligands can be tailored as an optical adjuvant for reporting signal reference. For benefits, the comprehensive functions leaned on the catalytic performance and optical reference property from Pt<sup>NW</sup>@PCN-222 can be harvested for a ratiometric glycoprotein assay. Besides, due to the variant catalytic converter of Pt<sup>NW</sup>@PCN-222 involved in the two fluorogenic reactions, the proposed glycoprotein assay exhibited a range of 0.03-3 nM with a detection limit of 7.91 pM in the reductive pathway, and showed a linear range from 0.06 to 10 nM with a detection limit of 21.64 pM in the oxidative pathway. Collectively, our proposed glycoprotein assay may provide a new thought in opto/catalytic MOF adjuvant-empowered ratiometric sensing in the dual-path reflection manner, which may also reinforce the accurate detection capability for the glycoprotein assay.

Authors

Institutions

Publication Details

Journal
Analytical Chemistry
Published
2026-02-04
DOI
https://doi.org/10.1021/acs.analchem.5c06805
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Porphyrinic Metal–Organic Frameworks with Longitudinal Pt Deposition Referenced as Opto/Catalytic Adjuvants for Dual-Path Glycoprotein Assay

Licheng Yu, L. X. Chen, Hao Wang, Xiwen He et al.
Analytical Chemistry
Advanced biosensing and bioanalysis techniques
article

Porphyrinic Metal–Organic Frameworks with Longitudinal Pt Deposition Referenced as Opto/Catalytic Adjuvants for Dual-Path Glycoprotein Assay

Licheng Yu, L. X. Chen, Hao Wang, Xiwen He, Yukui Zhang, Yi Yang, Pengli Bai, Liang He
article en

Abstract

In this work, porphyrinic metal-organic frameworks (MOFs) with longitudinal Pt deposition were developed for the inspired establishment of opto/catalytic adjuvants referenced for a dual-path glycoprotein assay. In the compositional cooperation, porphyrinic MOFs were synthesized through Zr oxoclusters and polytopic porphyrin ligands into a benchmark template (PCN-222), followed by catalytic Pt nanowire deposition (Pt<sup>NW</sup>@PCN-222). As for signal reflection, the fluorogenic species (i.e., resazurin and amplex red) were integrated into zeolitic imidazolate framework-8 (ZIF-8) via epitaxial shell growth to guide lectin integration. The specific performance toward glycoprotein recognition was guaranteed by both antibody-antigen interaction as well as glycan epitope binding through lectin affinity, and the signal response was initiated by textural decomposition of the ZIF-8 skeleton in a controllable manner. On one hand, Pt<sup>NW</sup>@PCN-222 can function as the catalytic adjuvant to exert the fluorogenic reactions: a reductive <i>N</i>-deoxygenation of resazurin and an oxidative <i>N</i>-deacetylation of amplex red, in which both the redox reactions generated the fluorescent species of resorufin products. On the other hand, Pt<sup>NW</sup>@PCN-222 with endogenous periodical arrangement of porphyrin ligands can be tailored as an optical adjuvant for reporting signal reference. For benefits, the comprehensive functions leaned on the catalytic performance and optical reference property from Pt<sup>NW</sup>@PCN-222 can be harvested for a ratiometric glycoprotein assay. Besides, due to the variant catalytic converter of Pt<sup>NW</sup>@PCN-222 involved in the two fluorogenic reactions, the proposed glycoprotein assay exhibited a range of 0.03-3 nM with a detection limit of 7.91 pM in the reductive pathway, and showed a linear range from 0.06 to 10 nM with a detection limit of 21.64 pM in the oxidative pathway. Collectively, our proposed glycoprotein assay may provide a new thought in opto/catalytic MOF adjuvant-empowered ratiometric sensing in the dual-path reflection manner, which may also reinforce the accurate detection capability for the glycoprotein assay.

Analytical ChemistryVol. 98(6)
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Nankai University (CN), Suzhou Institute of Biomedical Engineering and Technology (CN)
Partnerships for the goals
Openalex Percentile: Top 67%
Advanced biosensing and bioanalysis techniques
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.