Visualization of Protein–Protein Interaction In Situ Using Hybridization-Enhanced Proximity Ligation Assay

Understanding protein-protein interactions (PPIs) is critical for elucidating cellular functions and disease mechanisms. We present the hybridization-enhanced proximity ligation assay (HPLA), a novel approach incorporating a prehybridization step to improve the ligation efficiency of DNA probes on antibody-oligonucleotide conjugates. This step involves a splint probe hybridizing with complementary sequences on the DNA probes bound to interacting protein complexes, forming V-shaped overhangs that facilitate the circularization of two circle probes. These circularized DNA templates undergo localized rolling circle amplification, producing amplification products that can be visualized as fluorescent dots upon hybridization with dye-labeled detection probes. We demonstrated the utility of HPLA in various biological contexts, including cancer-associated protein interactions and signaling pathways, achieving clearer, more precise visualization of PPIs and enabling robust quantitative analysis.

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Publication Details

Journal
Analytical Chemistry
Published
2024-12-07
DOI
https://doi.org/10.1021/acs.analchem.4c04229
Citations
3
Primary Topic
Biotin and Related Studies
Type
article
Field-Weighted Citation Impact
0.98

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article

Visualization of Protein–Protein Interaction In Situ Using Hybridization-Enhanced Proximity Ligation Assay

Rongqin Ke, Weilin Zheng, Jiayu Chen, Chen Lin et al.
3 citations
Analytical Chemistry
Biotin and Related Studies
0.98
article

Visualization of Protein–Protein Interaction In Situ Using Hybridization-Enhanced Proximity Ligation Assay

Rongqin Ke, Weilin Zheng, Jiayu Chen, Chen Lin, Xiaojie He, Yanxiu Liu, Yinghui Qiu, Yang Yu
article en
3 citations

Abstract

Understanding protein-protein interactions (PPIs) is critical for elucidating cellular functions and disease mechanisms. We present the hybridization-enhanced proximity ligation assay (HPLA), a novel approach incorporating a prehybridization step to improve the ligation efficiency of DNA probes on antibody-oligonucleotide conjugates. This step involves a splint probe hybridizing with complementary sequences on the DNA probes bound to interacting protein complexes, forming V-shaped overhangs that facilitate the circularization of two circle probes. These circularized DNA templates undergo localized rolling circle amplification, producing amplification products that can be visualized as fluorescent dots upon hybridization with dye-labeled detection probes. We demonstrated the utility of HPLA in various biological contexts, including cancer-associated protein interactions and signaling pathways, achieving clearer, more precise visualization of PPIs and enabling robust quantitative analysis.

Analytical ChemistryVol. 96(50)
Huaqiao University (CN)
Xiamen Municipal Bureau of Science and Technology, Natural Science Foundation of Fujian Province, Huaqiao University, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 25%
Biotin and Related Studies
0.98
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