An insight into embryogenesis interruption by carbon nitride dots: can they be nucleobase analogs?

  • Yiqun Zhou
  • , Jiuyan Chen
  • , Emel Kirbas Cilingir
  • , Wei Zhang
  • , Lemay Gonzalez
  • , Samuel Perez
  • , Arjuna Davila
  • , Nicholas Brejcha
  • , Jun Gu
  • , Wenquan Shi
  • , Justin B. Domena
  • , Braulio C.L.B. Ferreira
  • , Fuwu Zhang
  • , Frederic A. Vallejo
  • , Daniela Toledo
  • , Piumi Y. Liyanage
  • , Regina M. Graham
  • , Julia Dallman
  • , Zhili Peng
  • , Christian Agatemor
  • Alessandro Catenazzi, Roger M. Leblanc

Research output: Contribution to journalArticlepeer-review

Abstract

The carbon nitride dot (CND) is an emerging carbon-based nanomaterial. It possesses rich surface functional moieties and a carbon nitride core. Spectroscopic data have demonstrated the analogy between CNDs and cytosine/uracil. Recently, it was found that CNDs could interrupt the normal embryogenesis of zebrafish. Modifying CNDs with various nucleobases, especially cytosine, further decreased embryo viability and increased deformities. Physicochemical property characterization demonstrated that adenine- and cytosine-incorporated CNDs are similar but different from guanine-, thymine- and uracil-incorporated CNDs in many properties, morphology, and structure. To investigate the embryogenesis interruption at the cellular level, bare and different nucleobase-incorporated CNDs were applied to normal and cancerous cell lines. A dose-dependent decline was observed in the viability of normal and cancerous cells incubated with cytosine-incorporated CNDs, which matched results from the zebrafish embryogenesis experiment. In addition, nucleobase-incorporated CNDs were observed to enter cell nuclei, demonstrating a possibility of CND-DNA interactions. CNDs modified by complementary nucleobases could bind each other via hydrogen bonds, which suggests nucleobase-incorporated CNDs can potentially bind the complementary nucleobases in a DNA double helix. Nonetheless, neither bare nor nucleobase-incorporated CNDs were observed to intervene in the amplification of the zebrafish polymerase-alpha 1 gene in quantitative polymerase chain reactions. Thus, in conclusion, the embryogenesis interruption by bare and nucleobase-incorporated CNDs might not be a consequence of CND-DNA interactions during DNA replication. Instead, CND-Ca2+ interactions offer a plausible mechanism that hindered cell proliferation and zebrafish embryogenesis originating from disturbed Ca2+ homeostasis by CNDs. Eventually, the hypothesis that raw or nucleobase-incorporated CNDs can be nucleobase analogs proved to be invalid.

Original languageEnglish
Pages (from-to)17607-17624
Number of pages18
JournalNanoscale
Volume14
Issue number47
DOIs
StatePublished - Nov 17 2022
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2022 The Royal Society of Chemistry.

ASJC Scopus Subject Areas

  • General Materials Science

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