Batista Josiane A D, de Oliveira Rayane M, Lima Carlos H M, Lana Júnior Milton L, Dos Anjos Virgílio C, Bell Maria J V, Rocha Márcio S
Departamento de Física, Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil.
Departamento de Física, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
Beilstein J Nanotechnol. 2025 Feb 14;16:187-194. doi: 10.3762/bjnano.16.15. eCollection 2025.
We use optical tweezers and atomic force microscopy to investigate the potential of rare earth elements to be used as anticancer agents in the development of new chemotherapeutic drugs by characterizing the binding of three rare earths (ytterbium, neodymium, and erbium) to double-stranded DNA, which is one of the main targets for these drugs inside cells. The three elements presented a significant interaction with the biopolymer in buffers of physiological relevance, typically binding with very high equilibrium association constants (10 to 10 M) at the DNA grooves. Furthermore, neodymium and erbium can also induce a very strong compaction/condensation of the double helix at high concentrations, promoting DNA collapse at the single molecule level in a similar way to what occurs with classical DNA condensing agents such as polycations and depletants.
我们使用光镊和原子力显微镜,通过表征三种稀土元素(镱、钕和铒)与双链DNA的结合情况,来研究稀土元素在新型化疗药物开发中作为抗癌剂的潜力,双链DNA是这些药物在细胞内的主要作用靶点之一。这三种元素在具有生理相关性的缓冲液中与生物聚合物呈现出显著的相互作用,通常在DNA沟槽处以非常高的平衡缔合常数(10⁶至10⁷M⁻¹)结合。此外,钕和铒在高浓度下还能诱导双螺旋发生非常强烈的压缩/凝聚,在单分子水平上促进DNA塌陷,其方式类似于传统的DNA凝聚剂如聚阳离子和耗尽剂所发生的情况。