Repozytorium

A novel branched TAT47-57 peptide for selective Ni2+ introduction into the human fibrosarcoma cell nucleus.

Autorzy

Łukasz Szyrwiel

Mari Shimura

Junko Shirataki

Satoshi Matsuyama

Akihiro Matsunaga

Bartosz Setner

Łukasz Szczukowski

Zbigniew Szewczuk

Kazuto Yamauchi

Wiesław Malinka

Laurent Chavatte

Ryszard Łobiński

Rok wydania

2015

Czasopismo

Metallomics

Numer woluminu

7

Strony

1155-1162

DOI

10.1039/c5mt00021a

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

A TAT47–57 peptide was modified on the N-terminus by elongation with a 2,3-diaminopropionic acid residue and then by coupling of two histidine residues on its N-atoms. This branched peptide could bind to Ni under physiological conditions as a 1 : 1 complex. We demonstrated that the complex was quantitatively taken up by human fibrosarcoma cells, in contrast to Ni2+ ions. Ni localization (especially at the nuclei) was confirmed by imaging using both scanning X-ray fluorescence microscopy and Newport Green fluorescence. A competitive assay with Newport Green showed that the latter displaced the peptide ligand from the Ni-complex. Ni2+ delivered as a complex with the designed peptide induced substantially more DNA damage than when introduced as a free ion. The availability of such a construct opens up the way to investigate the importance of the nucleus as a target for the cytotoxicity, genotoxicity or carcinogenicity of Ni2+.

Adres publiczny

http://dx.doi.org/10.1039/c5mt00021a

Strona internetowa wydawcy

https://global.oup.com/?cc=pl

Strona internetowa wydawcy

https://www.rsc.org/

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