肽
DNA
K562细胞
部分
化学
生物物理学
髓系白血病
分子生物学
细胞
组合化学
生物化学
立体化学
生物
癌症研究
作者
Kazuharu Sugawara,Kenta Takeda,Hideki Kuramitz
标识
DOI:10.1002/elan.202300066
摘要
Abstract To electrochemically measure human myeloid leukemia cells (K562 cells), we constructed a probe consisting of peptide/single‐strand (ss) DNA. Ac‐H 6 Y 4 C with an acetylated N‐terminal of peptide was used to enhance the probe to allow electrode responses that could detect target cells. A ss‐DNA was selected as the target cell recognition moiety. The probe exhibits properties that combine the functionalities of both DNA and peptides. The measurement principle is based on changes in the peak currents of the peptide moieties that are caused by interactions between the ss‐DNA and target cells. The peak currents were proportional to the concentration of K 562 cells that ranged from 10 to 2,000 cells/mL with a LOD of 3 cells/mL.
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