Stability-Based Proteomics for Investigation of Structured RNA–Protein Interactions

Abstract

RNA−protein interactions are essential to RNA function throughout biology. Identifying the protein interactions associated with a specific RNA, however, is currently hindered by the need for RNA labeling or costly tiling-based approaches. Conventional strategies, which commonly rely on affinity pulldown approaches, are also skewed to the detection of high affinity interactions and frequently miss weaker interactions that may be biologically important. Reported here is the first adaptation of stability-based mass spectrometry methods for the global analysis of RNA−protein interactions. The stability of proteins from rates of oxidation (SPROX) and thermal protein profiling (TPP) methods are used to identify the protein targets of three RNA ligands, the MALAT1 triple helix (TH), a viral stem loop (SL), and an unstructured RNA (PolyU), in LNCaP nuclear lysate. The 315 protein hits with RNA-induced conformational and stability changes detected by TPP and/or SPROX were enriched in previously annotated RNA-binding proteins and included new proteins for hypothesis generation. Also demonstrated are the orthogonality of the SPROX and TPP approaches and the utility of the domain-specific information available with SPROX. This work establishes a novel platform for the global discovery and interrogation of RNA−protein interactions that is generalizable to numerous biological contexts and RNA targets.

Pt-Ru bimetallic nanoclusters with peroxidase-like activity for antibacterial therapy

“…In recent years, nanomaterials that mimic natural enzyme activity, known as nanozymes, have become a new strategy for combating microbial infections [9,10]. Nanozymes are nanomaterials that replace natural enzymes by simulating the coordination environment of catalytic sites [11][12][13][14][15][16][17]. Due to their broad-spectrum antibacterial activity, low drug resistance, and high stability, nanozymes have many excellent properties [18,19].…”