Abstract

This work deals with molecular dynamics analysis of properties of systems composed of carbon nanotubes and short telomeric DNA strands able to fold into i-motif structures at slightly acidic pH conditions. The studies are focused on possible application of such constructs as pH-controlled drug delivery and release systems. We study two different approaches. The first assumes that folding/unfolding property of these DNA strands might realize a gate closing/opening mechanism with carbon nanotube as a container for drug molecules. The second approach assumes that these DNA strands can modulate the drug intercalating property as a function of pH. As a model drug molecule we used doxorubicin. We found that the first approach is impossible to realize because doxorubicin is not effectively locked in the nanotube interior by DNA oligonuceotides. The second approach is more promising though direct drug release was not observed in unbiased molecular dynamics simulations. However, by applying detailed analysis of pair interaction energies, mobilities and potential of mean force we can show that doxorubicin can be released when the DNA strands fold into i-motifs. Carbon nanotube in that latter case acts mainly as a carrier for active phase which is composed of DNA fragments able to fold into noncanonical tetraplexes (i-motif).

Highlights

  • The cytosine-rich DNA oligomeres are able to perform reversible structural transitions as a function of pH [1,2,3]

  • This work deals with molecular dynamics analysis of properties of systems composed of carbon nanotubes and short telomeric DNA strands able to fold into i-motif structures at slightly acidic pH conditions

  • We found that the first approach is impossible to realize because doxorubicin is not effectively locked in the nanotube interior by DNA oligonuceotides

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Summary

Introduction

The cytosine-rich DNA oligomeres are able to perform reversible structural transitions as a function of pH [1,2,3]. Telomeric sequences of cytosine-rich strands were quite extensively studied as pH-controlled carriers of drugs. That choice is justified by quite intense studies related to application of carbon nanotubes as drugs carriers [23,24,25] and to the reported specific interaction of CNTs with DNA motifs [5,6,18,21] As a model drug we still use doxorubicin, partially due to already mentioned reasons, and due to already confirmed ability to control DOX release from carbon nanotubes by pH change of the environment [23,24,26]. We first analyze a gate opening/closing mechanism by cytosine-rich telomeric DNA sequences and carbon nanotube as DOX storage platform. We focus on the closer analysis of the interaction sites of DOX on i-motif and determine potential of mean force associated with the adsorption of DOX on these cytosine-rich DNA fragments

Definitions of the Analyzed Systems and Computational Details
A B1 B2 B3 B4 C1 C2 C3 C4
Co-Adsorption of I-Motif and Doxorubicin on the Surface of Carbon Nanotube
B2 B3 B4
Interaction of Doxorubicin with iMu and iMp
C2 C3 C4
Detachment of DOX from iM in Biased Calculations
Conclusions
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