Ayyub Omar B, Kofinas Peter
Fischell Department of Bioengineering, University of Maryland , College Park, Maryland 20742, United States.
ACS Nano. 2015 Aug 25;9(8):8004-11. doi: 10.1021/acsnano.5b01514. Epub 2015 Jul 23.
The passive monitoring of biological environments by soft materials has a variety of nanobiotechnology applications; however, invoking distinct transitions in geometric, mechanical or optical properties remains a prevalent design challenge. We demonstrate here that close-packed nanoparticle-hydrogel composites can progress through a substantial shift in such properties by the use of a chemical-to-physical cross-link transition mediated by the catalytic activity of different proteases. Catalytic cleavage of the original hydrogel network structure initiates the self-assembled formation of a secondary, physically cross-linked network, causing a 1200% increase in storage modulus. Furthermore, this unique mechanism can be fabricated as a 3D photonic crystal with broad (∼240 nm), visible responses to the targeted enzymes. Moreover, the material provided threshold responses, requiring a certain extent of proteolytic activity before the transition occurred. This allowed for the fabrication of Boolean logic gates (OR and AND), which responded to a specific assortment of proteases. Ultimately, this mechanism enables the design of stimuli-responsive hydrogels, which can proceed through a secondary network formation, after an energetic barrier has been breached. Protease responsive hydrogel nanocomposites, described here, could offer avenues in degradation-stiffening and collapsing materials for a variety of biomaterial applications.
通过软材料对生物环境进行被动监测具有多种纳米生物技术应用;然而,引发几何、机械或光学性质的明显转变仍然是一个普遍存在的设计挑战。我们在此证明,通过使用由不同蛋白酶的催化活性介导的化学交联到物理交联的转变,紧密堆积的纳米颗粒 - 水凝胶复合材料可以在这些性质上发生显著变化。原始水凝胶网络结构的催化裂解引发了二级物理交联网络的自组装形成,导致储能模量增加1200%。此外,这种独特的机制可以被制作为对靶向酶具有宽泛(约240纳米)可见响应的三维光子晶体。而且,该材料提供阈值响应,在转变发生之前需要一定程度的蛋白水解活性。这使得能够制造对特定种类蛋白酶有响应的布尔逻辑门(或门和与门)。最终,这种机制能够设计出刺激响应水凝胶,在突破能量障碍后可以通过二级网络形成过程。本文所述的蛋白酶响应水凝胶纳米复合材料可为各种生物材料应用中的降解 - 硬化和塌陷材料提供途径。