DNA Tetrahedron Mass-Tagged Probe Set for the Programmed Detection of Protein Trimers by Point-to-Point Recognition and Induced Self-Assembly in Living Cells

Abstract

Multimeric proteins normally perform different biological functions from their monomer components. Thus, precise recognition and quantitative detection of multimeric proteins can benefit a better understanding of complex biological processes and their roles in disease diagnosis and treatment. The challenge herein is to distinguish the multimeric proteins containing identical monomer components and recognize all the monomers in a multimeric protein on spatial scales. This situation is likely to become more significant for homomultimeric proteins. In this study, a DNA polyhedron mass-tagged probe set strategy was developed for the programmed detection of multimeric proteins in living cells. The probe set comprised recognition and displacement probes, a DNA polyhedron probe, and a mass-tagged probe. After point-to-point recognition of each monomer in the target protein complex by recognition and displacement probes, the DNA polyhedron probe could integrate the information on all the protein monomers by carrying out induced self-assembly via a cascaded toehold-mediated strand-displacement (TMSD) reaction. Afterward, the mass-tagged probe collected the integrated information, and the mass tag in the probe was released by ultraviolet (UV) irradiation and detected by mass spectrometry (MS). Using the tmTNF-α homotrimer as an example, its expression levels in different breast cancer cell lines were ultimately determined using this probe set containing a DNA tetrahedron probe. This study is among the first to quantitatively detect multimeric proteins in living cells. Using a similar strategy, more DNA polyhedron mass-tagged probe sets can be developed for the detection of higher-order multimeric proteins.