NanoBio Lab, Institute of Materials Research and Engineering, Agency for Science, Technology and Research (A*STAR), 31 Biopolis Way, The Nanos, #09-01, Singapore, 138669, Singapore.
NanoBio Lab, A*STAR Infectious Diseases Labs, A*STAR, 31 Biopolis Way, The Nanos, #09-01, Singapore, 138669, Singapore.
Small. 2023 Mar;19(12):e2205909. doi: 10.1002/smll.202205909. Epub 2023 Jan 1.
Under a pH value lower than the pK of adenine (3.5), adenine-rich sequences (A-strand) form a unique parallel A-motif duplex due to the protonation of A-strand. At a pH above 3.5, deprotonation of adenines leads to the dissolution of A-motif duplex to A-strand single coil. This pH-reconfigurable A-motif duplex has been developed as a novel pH-responsive DNA hydrogel, termed A-hydrogel. The hydrogel state is achieved at pH 1.2 by the A-motif duplex bridging units, which are cross-linked by both reverse Hoogsteen interaction and electrostatic attraction. Hydrogel-to-solution transition is triggered by pH 4.3 due to the deprotonation-induced separation of A-motif duplex. The A-hydrogel system undergoes reversible hydrogel-solution transitions by subjecting the system to cyclic pH shifts between 1.2 and 4.3. An anti-inflammatory medicine, sulfasalazine (SSZ), which intercalates into A-motif duplex, is loaded into A-hydrogel. Its pH-controlled release from A-hydrogel is successfully demonstrated. The strong acid-induced A-hydrogel may fill the gap that other mild acid-responsive DNA hydrogels cannot do, such as protection of orally delivered drug in hostile stomach environment against strong acid (pH ~ 1.2) and digestive enzymes.
在 pH 值低于腺嘌呤的 pK 值(3.5)时,由于 A 链的质子化,富含腺嘌呤的序列(A 链)形成独特的平行 A 基序双链。在 pH 值高于 3.5 时,腺嘌呤的去质子化导致 A 基序双链解链为 A 链单链。这种 pH 可重构的 A 基序双链已被开发为一种新型的 pH 响应性 DNA 水凝胶,称为 A 水凝胶。水凝胶状态是通过 A 基序双链桥接单元在 pH 1.2 时实现的,这些桥接单元通过反向 Hoogsteen 相互作用和静电吸引交联。由于去质子化诱导的 A 基序双链分离,pH 4.3 触发水凝胶到溶液的转变。A 水凝胶系统通过在 1.2 和 4.3 之间进行循环 pH 变化,经历可逆的水凝胶-溶液转变。将抗炎药物柳氮磺胺吡啶(SSZ)加载到 A 水凝胶中,它可以插入到 A 基序双链中。成功地证明了其从 A 水凝胶中的 pH 控制释放。强酸诱导的 A 水凝胶可以填补其他弱酸响应性 DNA 水凝胶无法填补的空白,例如在恶劣的胃环境中保护口服药物免受强酸(pH~1.2)和消化酶的侵害。