<p>There is considerable interest in the ability to modulate biological processes with magnetic fields. Here we demonstrate a strategy for selecting aptamers that exhibit enhanced binding to paramagnetic metal ions under a strong magnetic field. Using a high-magnetic-field (HM)-SELEX method targeting Co<sup>2+</sup>, we identified two classes of aptamers with magnetically-modulated binding behavior. One displayed a gradual 2–3-fold increase in affinity as magnetic field strength increased, while the other went from minimal target binding at ambient field strength to an affinity of ~200 μM at ≥ 6 T. Molecular simulations revealed that the magnetic field induces a global conformational rearrangement by enhancing aptamer-metal electrostatic interactions, optimizing the coordination geometry of the nucleotides. Chemical footprinting and mutational analysis confirmed the role of certain conformational changes in magnetically-induced ion binding. These results suggest opportunities to generate aptamer switches that can be used to manipulate biorecognition processes via an externally applied magnetic field in diverse applications.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Aptamers with magnetically tunable affinity for divalent cobalt ions

  • Shengjie Gao,
  • Lu Wang,
  • Lili Yao,
  • Yu Mao,
  • Michael Eisenstein,
  • Hyongsok Tom Soh,
  • Lei Zheng

摘要

There is considerable interest in the ability to modulate biological processes with magnetic fields. Here we demonstrate a strategy for selecting aptamers that exhibit enhanced binding to paramagnetic metal ions under a strong magnetic field. Using a high-magnetic-field (HM)-SELEX method targeting Co2+, we identified two classes of aptamers with magnetically-modulated binding behavior. One displayed a gradual 2–3-fold increase in affinity as magnetic field strength increased, while the other went from minimal target binding at ambient field strength to an affinity of ~200 μM at ≥ 6 T. Molecular simulations revealed that the magnetic field induces a global conformational rearrangement by enhancing aptamer-metal electrostatic interactions, optimizing the coordination geometry of the nucleotides. Chemical footprinting and mutational analysis confirmed the role of certain conformational changes in magnetically-induced ion binding. These results suggest opportunities to generate aptamer switches that can be used to manipulate biorecognition processes via an externally applied magnetic field in diverse applications.