PREDICTOR: A Non-Enzymatic Catalytic Cascade Tool for in Situ Visualization of Small Extracellular Vesicle Surface glycoRNAs

  • J Extracell Vesicles. 2026 Apr;15(4):e70282. doi: 10.1002/jev2.70282.
Shuang Xie  1 Ben Niu  1 Ruijia Deng  1 Liu Feng  1 Zuowei Xie  1 Shuang Zhao  1 Hongzhao Yang  1 Meilin Gong  1 Jing Sheng  1 Ligai Zhang  1 Yan Pi  2 Ningtao Cheng  3 Ming Chen  1 Kai Chang  1  4
Affiliations
  • 1. Department of Clinical Laboratory Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
  • 2. Department of Rehabilitation Medicine, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • 3. School of Public Health, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
  • 4. State Key Laboratory of Trauma and Chemical Poisoning, Army Medical University, Chongqing, China.
Abstract

Glycosylated RNAs (glycoRNAs) are membrane-displayed RNA-glycan conjugates, but quantitative in situ analysis of low-abundance glycoRNAs on small extracellular vesicles (sEVs) remains challenging. Here, we develop PREDICTOR (proximity-encoded non-linear hybridization chain reaction circuit), an enzyme-free catalytic DNA cascade for imaging and quantifying surface glycoRNAs on intact sEVs. PREDICTOR uses a sialic acid aptamer and an RNA-sequence probe as split recognition modules, whose proximity on a single glycoRNA reconstitutes an initiator that drives dendritic DNA self-assembly and non-linear fluorescence amplification on the sEV surface. Across serial sEV inputs (5×103-5×109 particles·mL- 1), PREDICTOR exhibited a steeper concentration-response than representative amplification assays, with higher regression slopes in bulk fluorescence (0.372, R2 = 0.9846) compared with ARPLA (0.301, R2 = 0.9748) and HieCo 2 (0.230, R2 = 0.9663), and similarly improved performance in bead-based imaging (4.105, R2 = 0.9816 vs. 3.495 and 2.711). Applying PREDICTOR to a breast Cancer transformation model (MCF-10A → MCF-7 → MDA-MB-231) showed that multiple surface glycoRNA candidates decrease with malignancy, accompanied by progressive softening of sEV membranes (Young's modulus reduced by 25.08% and 54.72%). Functionally, enzymatic depletion of surface RNA and disruption of sialylated N-glycan features attenuated macrophage uptake and inflammatory activation, supporting a contribution of surface glycoRNAs to sEV recognition. Collectively, PREDICTOR provides a rapid, enzyme-free platform for quantitative and spatial profiling of sEV surface glycoRNAs and links their abundance to vesicle mechanics and immune-cell interactions.

Keywords
DNA nanotechnology; glycoRNAs; in situ visualization; non‐enzymatic cascade amplification; small extracellular vesicles.
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