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光介导肟连接作为一种用于时空控制水凝胶形成和修饰的生物正交工具。

Photomediated oxime ligation as a bioorthogonal tool for spatiotemporally-controlled hydrogel formation and modification.

作者信息

Farahani Payam E, Adelmund Steven M, Shadish Jared A, DeForest Cole A

机构信息

Department of Chemical Engineering, University of Washington, 4000 15th Ave NE, Seattle, WA 98195, USA.

出版信息

J Mater Chem B. 2017 Jun 21;5(23):4435-4442. doi: 10.1039/c6tb03400d. Epub 2017 Apr 4.

Abstract

Click chemistry has proved a valuable tool in biocompatible hydrogel formation for 3D cell culture, owing to its bioorthogonal nature and high efficiency under physiological conditions. While traditional click reactions can be readily employed to create uniform functional materials about living cells, their spontaneity prohibits spatiotemporal control of material properties, thereby limiting their utility in recapitulating the dynamic heterogeneity characteristic of the in vivo microenvironment. Photopolymerization-based techniques gain this desired level of 4D programmability, but often at the expense of introducing propagating free radicals that are prone to non-specific reactions with biological systems. Here we present a strategy for bioorthogonal hydrogel formation and modification that does not rely on propagating free radicals, proceeding through oxime ligation moderated by a photocaged alkoxyamine. Upon mild near UV light exposure, the photocage is cleaved, liberating the alkoxyamine and permitting localized condensation with an aldehyde. Multi-arm crosslinkers, functionalized with either benzaldehydes or photocaged alkoxyamines, formed oxime-based hydrogels within minutes of light exposure in the presence of live cells. Polymerization rates and final mechanical properties of these gels could be systematically tuned by varying crosslinker concentrations, light intensity, aniline catalyst equivalents, and pH. Moreover, hydrogel geometry and final mechanical properties were controlled by the location and extent of UV exposure, respectively. Photomediated oxime ligation was then translated to the biochemical modification of hydrogels, where full-length proteins containing photocaged alkoxyamines were immobilized in user-defined regions exposed to UV light. The programmability afforded by photomediated oxime ligation can recapitulate dynamically anisotropic mechanical and biochemical aspects of the native extracellular matrix. Consequently, photopolymerized oxime-based hydrogels are expected to enable an enhanced understanding of cell-matrix interactions by serving as improved 4D cell culture platforms.

摘要

点击化学已被证明是用于3D细胞培养的生物相容性水凝胶形成的一种有价值的工具,这得益于其生物正交性和在生理条件下的高效率。虽然传统的点击反应可很容易地用于创建关于活细胞的均匀功能材料,但其自发性阻碍了对材料特性的时空控制,从而限制了它们在重现体内微环境动态异质性特征方面的效用。基于光聚合的技术获得了这种所需的4D可编程性水平,但往往以引入易于与生物系统发生非特异性反应的传播自由基为代价。在这里,我们提出了一种用于生物正交水凝胶形成和修饰的策略,该策略不依赖于传播自由基,而是通过由光笼蔽烷氧基胺调节的肟连接来进行。在温和的近紫外光照射下,光笼被裂解,释放出烷氧基胺并允许其与醛进行局部缩合。用苯甲醛或光笼蔽烷氧基胺功能化的多臂交联剂在活细胞存在下光照几分钟内形成基于肟的水凝胶。这些凝胶的聚合速率和最终机械性能可通过改变交联剂浓度、光强度、苯胺催化剂当量和pH值进行系统调节。此外,水凝胶的几何形状和最终机械性能分别由紫外线照射的位置和程度控制。然后,光介导的肟连接被转化为水凝胶的生化修饰,其中含有光笼蔽烷氧基胺的全长蛋白质被固定在暴露于紫外光的用户定义区域。光介导的肟连接所提供的可编程性可以重现天然细胞外基质的动态各向异性机械和生化方面。因此,光聚合的基于肟的水凝胶有望通过作为改进的4D细胞培养平台来增强对细胞-基质相互作用的理解。

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