# Interaction of Carbon Dots with Nucleic Acids Is Driven by Their Surface Charge

## TL;DR

This study explores how carbon dots interact with nucleic acids, finding that surface charge and size are key factors affecting their binding behavior.

## Contribution

The study reveals that positively charged carbon dots bind tightly to nucleic acids, offering insights for designing optimized theranostic materials.

## Key findings

- Positively charged carbon dots (CD+) remain tightly bound to nucleic acids.
- Nonspecific interactions occur without disrupting nucleic acid structures.
- CD+ can bridge adjacent DNA gyres in nucleosomes, potentially altering chromatin dynamics.

## Abstract

Carbon dots (CDs)
are nanoscale carbon materials with tunable optical
properties, low toxicity, and modular functionalization, making them
a promising material for biomedical applications. For safe and efficient
applications in theranostics, it is essential to assess how CDs interact
with biomolecules. Here, we focus on the effect of CDs on the structure
and function of nucleic acids (NAs), relevant to NA structural stability,
chromatin organization, and gene regulation. We performed more than
150 μs of atomistic molecular dynamics simulations, encompassing
a diverse set of NA structures, from canonical DNA and RNA helices
through noncanonical motifs such as tetraloops and G-quadruplexes,
up to nucleosomes. We simulated their interactions with graphitic
CDs with two sizes and distinct surface chemistries: neutral hydrophobic
(CD0), negatively charged (CD–), and
positively charged (CD+). We identified multiple nonspecific
interaction modes including stacking to bases, CH−π contacts,
and electrostatic interactions with the NA backbone. All CD types
formed contacts with NAs, but only CD+ remained tightly
bound and is therefore relevant for NA-related applications. The CD
nonspecific binding did not compromise the global NA architecture,
and we did not observe any intercalation or base-pair disruption.
In the nucleosome, CD+ adsorb to DNA and occasionally bridge
adjacent DNA gyres, that may alter local chromatin dynamics. In summary,
the surface charge and particle size emerged as the key determinants
of NA–CD interactions, providing atomistic guidance for the
rational design of CDs optimized for theranostic applications.