Skip to content
Open access

A Simple Method to Distinguish Active and Inactive Aptamers by Analyzing the Ruggedness of the Aptamer Free Energy Landscape

Aug 2026 · bioRxiv · 0 citations · 22 references
Biology

TL;DR

Results indicate that folding landscape organization can be used as a predictor of aptamer activity and establish RCI as a simple, mechanistically interpretable measure for improving candidate prioritization, especially in therapeutic aptamer discovery.

Abstract

Aptamers are structured nucleic acid ligands capable of high-affinity, high-specificity molecular recognition generated using variations of the SELEX (Systematic Evolution of Ligands by Exponential Enrichment) process. However, SELEX often produces sequences that enrich yet may lack binding efficacy. We propose a measure called the Ruggedness Composite Index (RCI) along with a method for computing it, that can be used to distinguish binding-competent (“active”) aptamers from weak or non-binding (“inactive”) aptamers. Given a set of aptamers, RCI incorporates information on their fragmentation (landscape partitioning), basin entropy (metastable state distribution), cumulative density irregularity (non-uniform occupancy), and structural–energy correlation length (structure– energy coupling scale). We test whether secondary-structure folding energy landscape topology distinguishes active from inactive aptamers using a multiscale level set framework across six datasets. Active aptamers show lower RCI values and occupy smoother, funnel-like conformational spaces, while inactive aptamers show higher RCI values, reflecting fragmented, high-entropy landscapes. By contrast, classical thermodynamic features, such as minimum free energy, show limited discrimination between active and inactive aptamers. In all datasets, sequences that exhibit enrichment which is not monotonic but lack specificity exhibit elevated ruggedness, indicating landscape topology can predict non-specific enrichment. These results indicate that folding landscape organization can be used as a predictor of aptamer activity and establish RCI as a simple, mechanistically interpretable measure for improving candidate prioritization, especially in therapeutic aptamer discovery.

Read PDF

Similar papers

Open access Sep 2026

APDB: A Large-Scale Repository of Predicted 2D and 3D Aptamer Structures

RNA aptamers are short, single-stranded oligonucleotides capable of folding into specific three-dimensional structures to bind diverse molecular targets with high affinity and specificity. In this study, we present a comprehensive computational analysis of a curated data set of over 150,000 RNA aptamers annotated with...

K. Mokgopa, Kevin A. Lobb, T. Tshiwawa · 0 citations
Open access Sep 2026

Extending Small-Molecule Aptamer Discovery Principles to Protein Targets: Selection and Characterization of Green Fluorescent Protein Aptamers.

Since the advent of systematic evolution of ligands by exponential enrichment (SELEX), numerous protein-binding aptamers have been reported, yet their binding characterizations are often less developed than those of small-molecule aptamers, limiting mechanistic understanding and practical applications. Here, we establi...

Stefen Stangherlin, Nathan Wong, Logan Fanning et al. · 0 citations
Open access Oct 2026

AntiCapt: Fine-Tuned Nucleotide Language Models for Predicting and Designing Anticancer Aptamers

Over the past decade, aptamers have emerged as promising therapeutics, with cancer therapeutics as a major research area. Existing computational methods, however, either predict aptamer-target pairs or design aptamers against a specific target. In this study, we present AntiCapt, a computational method for identifying...

N. Bajiya, Naman Kumar Mehta, G. Raghava · 0 citations
Open access Oct 2026

AutoHMD: Scalable and Accurate Validation of Antibody-Antigen Complexes by Heated Molecular Dynamics.

MOTIVATION Antibody-antigen (Ab-Ag) interactions are central to immune recognition and widely exploited in therapeutic design, making accurate structural characterization of these complexes a central challenge in the field. While docking and artificial intelligence-based approaches can generate multiple candidate bindi...

Júlia S. Souza, Aline O. Albuquerque, Diego Almeida et al. · 0 citations
Aug 2026

Resampling-Iteration-Evolution (RIE): A Rational Design System for Engineering High-Affinity Peptides against Small Molecules.

A computational design pipeline, termed resampling-iteration-evolution (RIE), for the rapid discovery of high-affinity molecular recognition peptides (MRPs) from large structural and sequence databases is reported, establishing RIE as a rapid and effective in silico platform for the development of peptide binders for s...

Li-Hong Yu, Yun Ma, Yue-Hong Pang et al. · 0 citations
Aug 2026

From Cross-Reactivity to Specificity: A SELEX-Derived Aptamer Sensor Array for Aristolochic Acid I and Aristolactam I

Aptamer selection often yields multiple sequence families that recognize different epitopes or bind through distinct molecular interactions. Rather than using a single aptamer for detection, we demonstrate that these complementary aptamers can be integrated into a cross-reactive sensor array to enhance molecular disc...

Yun Shu, Pan-Ting Sang, Shi-Yuan Liu et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.