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10.1002/smtd.202501936

http://scihub22266oqcxt.onion/10.1002/smtd.202501936
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41351211!?!41351211

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suck abstract from ncbi

pmid41351211      Small+Methods 2025 ; ? (?): e01936
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  • Characterization of Non-Specific Electrostatic Interactions of Cationic Peptides with DNA Origami and Their Functional Consequences #MMPMID41351211
  • Kang SH; Kwon O; Cho BK; Yoo S; Wang JM; Choi Y; Yoon HY; Choi J; Ryu JH
  • Small Methods 2025[Dec]; ? (?): e01936 PMID41351211show ga
  • The functionalization of DNA origami with peptides is a powerful strategy for creating nanodevices for therapeutic and diagnostic applications. A critical but often overlooked challenge is the non-specific electrostatic binding of cationic peptides to the anionic DNA nanostructure, which leads to uncontrolled stoichiometry and undermines functional predictability. Here, the study systematically characterizes this issue and demonstrates a practical purification strategy to mitigate it. It is quantitatively shown that cationic peptides associate with DNA origami in vast excess of their intended binding sites, a phenomenon not observed with anionic control peptides. This non-specific binding is confirmed to be electrostatic and is effectively screened by high salt. To address this, a charge-dependent purification approach is evaluated using polyethylene glycol (PEG) precipitation, showing that cationic peptides require extensive purification (>/=7 cycles), whereas anionic peptides need only minimal treatment (2 cycles) to achieve precise loading. Crucially, the study provides definitive functional evidence that a therapeutic peptide (brain-derived neurotrophic factor-mimicking peptide) must be attached via stable, site-specific hybridization to elicit a potent biological response; non-specifically adsorbed peptides are largely inactive. This work provides a set of critical design guidelines and purification considerations necessary for the rational design of reliable and functionally predictable DNA nanodevices.
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