DNA Dissipative System for Controlled Release of Immunostimulatory CpG Oligodeoxynucleotides

IF 4 Q2 ENGINEERING, BIOMEDICAL
Aman Ishaqat, Xiaofeng Zhang, Andreas Herrmann
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Abstract

Herein, a dissipative system tailored for the controlled loading and release of CpG oligodeoxynucleotides (CpG ODNs), known for their pharmacological immunostimulatory properties, is reported. The approach involves multiple cycles of deactivation and activation of the CpG ODNs via its hybridization with a complementary fuel strand, followed by its selective release mediated by the enzymatic activity of T7 exonuclease. The autonomous and temporal behavior of this dissipative system can be tuned by three factors: the design of the fuel strand and its concentration that governs the kinetics of the forward hybridization reaction, as well as the concentration of T7 exonuclease, which regulates the backward energy dissipation reaction. Furthermore, the enzyme's tolerance toward waste accumulation is demonstrated, and the system's robust performance when utilizing various fuel strands in alternating fashion is showcased. The findings underscore the potential of this approach for precise and programmable delivery of therapeutic nucleic acids in multiple cycles, with implications for enhancing immunotherapeutic strategies in which controlled kinetics of the nucleic acid is highly desired.

Abstract Image

用于控制释放免疫刺激性 CpG 寡聚氧核苷酸的 DNA 耗散系统
本文报告了一种耗散系统,该系统专为控制 CpG 寡聚氧核苷酸(CpG ODNs)的装载和释放而定制,CpG ODNs 因其药理免疫刺激特性而闻名。这种方法包括通过与互补燃料链杂交,使 CpG ODNs 失活和活化的多个循环,然后在 T7 外切酶的酶活性介导下选择性释放 CpG ODNs。这一耗散系统的自主和时间行为可由三个因素调节:燃料链的设计及其浓度(控制前向杂交反应的动力学),以及 T7 外切酶的浓度(控制后向能量耗散反应)。此外,还证明了该酶对废物积累的耐受性,并展示了该系统在交替使用各种燃料链时的强大性能。研究结果强调了这种方法在多周期精确和可编程递送治疗核酸方面的潜力,对加强免疫治疗策略具有重要意义,在这种策略中,核酸的可控动力学是非常必要的。
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来源期刊
Advanced Nanobiomed Research
Advanced Nanobiomed Research nanomedicine, bioengineering and biomaterials-
CiteScore
5.00
自引率
5.90%
发文量
87
审稿时长
21 weeks
期刊介绍: Advanced NanoBiomed Research will provide an Open Access home for cutting-edge nanomedicine, bioengineering and biomaterials research aimed at improving human health. The journal will capture a broad spectrum of research from increasingly multi- and interdisciplinary fields of the traditional areas of biomedicine, bioengineering and health-related materials science as well as precision and personalized medicine, drug delivery, and artificial intelligence-driven health science. The scope of Advanced NanoBiomed Research will cover the following key subject areas: ▪ Nanomedicine and nanotechnology, with applications in drug and gene delivery, diagnostics, theranostics, photothermal and photodynamic therapy and multimodal imaging. ▪ Biomaterials, including hydrogels, 2D materials, biopolymers, composites, biodegradable materials, biohybrids and biomimetics (such as artificial cells, exosomes and extracellular vesicles), as well as all organic and inorganic materials for biomedical applications. ▪ Biointerfaces, such as anti-microbial surfaces and coatings, as well as interfaces for cellular engineering, immunoengineering and 3D cell culture. ▪ Biofabrication including (bio)inks and technologies, towards generation of functional tissues and organs. ▪ Tissue engineering and regenerative medicine, including scaffolds and scaffold-free approaches, for bone, ligament, muscle, skin, neural, cardiac tissue engineering and tissue vascularization. ▪ Devices for healthcare applications, disease modelling and treatment, such as diagnostics, lab-on-a-chip, organs-on-a-chip, bioMEMS, bioelectronics, wearables, actuators, soft robotics, and intelligent drug delivery systems. with a strong focus on applications of these fields, from bench-to-bedside, for treatment of all diseases and disorders, such as infectious, autoimmune, cardiovascular and metabolic diseases, neurological disorders and cancer; including pharmacology and toxicology studies.
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