Kaletta Nastasja, Burick Sophia, Qudbuddin Yusuf, Schwille Petra
Department of Cellular and Molecular Biophysics, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT, 06511, USA.
Adv Sci (Weinh). 2025 Jun 27:e15510. doi: 10.1002/advs.202415510.
Wetting interactions between biomolecular condensates and lipid membranes have demonstrated great potential to induce large-scale membrane transformations in synthetic cells. However, the ability to functionalize existing condensates and control their interactions with membranes is limited, restricting their utility in engineering controlled wetting behavior. Here, fully programmable condensates based on DNA Y-motifs are introduced to engineer precisely tunable wetting behavior. In contrast to unmodified condensates that show no interaction with membranes, wetting of supported lipid bilayers (SLBs) can be induced by partial cholesterol-functionalization of DNA nanostructures. Incorporating photoactivatable DNA-lipid linker enables contact angles to be controlled over a wide range by varying UV exposure times. Furthermore, selective partitioning of small unilamellar vesicles (SUVs) into DNA condensates is demonstrated via programmable surface interactions. In giant unilamellar vesicles (GUVs), membrane wetting of enclosed condensates can be efficiently induced post-fabrication and results in outward budding. Thus, this work establishes programmable DNA condensates as a powerful platform for fine-tuned control over membrane-associated processes in synthetic cells, exceeding traditional approaches such as altering lipid composition or environmental conditions. Finally, the platform provides the possibility to design smart drug carriers for controlled substance delivery and release, and represents a customizable model to study condensate-membrane dynamics.
生物分子凝聚物与脂质膜之间的润湿相互作用已显示出在合成细胞中诱导大规模膜转变的巨大潜力。然而,对现有凝聚物进行功能化并控制其与膜相互作用的能力有限,限制了它们在工程可控润湿行为中的应用。在此,引入了基于DNA Y基序的完全可编程凝聚物,以设计精确可调的润湿行为。与未修饰的不与膜相互作用的凝聚物不同,DNA纳米结构的部分胆固醇功能化可诱导支持脂质双层(SLB)的润湿。引入光活化DNA-脂质连接体后,通过改变紫外线照射时间可在很宽的范围内控制接触角。此外,通过可编程的表面相互作用证明了小单层囊泡(SUV)可选择性地分配到DNA凝聚物中。在巨型单层囊泡(GUV)中,封闭凝聚物的膜润湿可在制备后有效诱导,并导致向外出芽。因此,这项工作将可编程DNA凝聚物确立为一个强大的平台,用于对合成细胞中与膜相关的过程进行微调控制,超越了改变脂质组成或环境条件等传统方法。最后,该平台为设计用于控制物质递送和释放的智能药物载体提供了可能性,并代表了一个可定制的模型来研究凝聚物-膜动力学。