Multi-Objective Design of DNA-Stabilized Nanoclusters Using Variational Autoencoders With Automatic Feature Extraction.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39288200.
- Also identified by DOI 10.1021/acsnano.4c09640 and PMC identifier 11447918.
- Licence recorded as CC BY-NC-ND.
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Abstract
DNA-stabilized silver nanoclusters (Ag<sub><i>N</i></sub>-DNAs) have sequence-tuned compositions and fluorescence colors. High-throughput experiments together with supervised machine learning models have recently enabled design of DNA templates that select for Ag<sub><i>N</i></sub>-DNA properties, including near-infrared (NIR) emission that holds promise for deep tissue bioimaging. However, these existing models do not enable simultaneous selection of multiple Ag<sub><i>N</i></sub>-DNA properties, and require significant expert input for feature engineering and class definitions. This work presents a model for multiobjective, continuous-property design of Ag<sub><i>N</i></sub>-DNAs with automatic feature extraction, based on variational autoencoders (VAEs). This model is generative, i.e., it learns both the forward mapping from DNA sequence to Ag<sub><i>N</i></sub>-DNA properties and the inverse mapping from properties to sequence, and is trained on an experimental data set of DNA sequences paired with Ag<sub><i>N</i></sub>-DNA fluorescence properties. Experimental testing shows that the model enables effective design of Ag<sub><i>N</i></sub>-DNA emission, including bright NIR Ag<sub><i>N</i></sub>-DNAs with 4-fold greater abundance compared to training data. In addition, Shapley analysis is employed to discern learned nucleobase patterns that correspond to fluorescence color and brightness. This generative model can be adapted for a range of biomolecular systems with sequence-dependent properties, enabling precise design of emerging biomolecular nanomaterials.
Medical subject headings
- DNA
- Silver
- Metal Nanoparticles