首页> 外文期刊>Analytical chemistry >Direct-Write Fabrication of Functional Protein Matrixes Using a Low-Cost Q-Switched Laser
【24h】

Direct-Write Fabrication of Functional Protein Matrixes Using a Low-Cost Q-Switched Laser

机译:使用低成本调Q激光器直接写功能蛋白基质

获取原文
获取原文并翻译 | 示例
       

摘要

We report the use of an inexpensive, small, and "turnkey" Q-switched 532-nm Nd:YAG laser as a source for nonlinear, direct-write protein microfabrication. In this approach, microJoule pulses (pulse widths, approx600 ps) are focused using high numerical aperture optics to submicrometer focal spots, creating instantaneous intensities great enough to promote multiphoton excitation of a photosensitizer and subsequent intermolecular crosslinking of protein molecules. By scanning the femtoliter focal volume through reagent solution, extended protein-based structures can be fabricated with precise, three-dimensional topographies. As with earlier studies using a femtosecond titanium:sapphire laser costing more than dollar100K, physically robust and chemically responsive microstructures can be fashioned rapidly with feature sizes smaller than 0.5 (mu)m, and cross-linking can be achieved using both biologically benign sensitizers (e.g., flavins) and by using the proteins themselves to sensitize cross-linking. We demonstrate in situ fabrication to corral neurite outgrowth and show the ability to functionalize avidin structures with biotinylated reagents, an approach that enables chemical sensing to be performed in specified microenvironments. Characterization of this inexpensive, low-power source will greatly broaden access to direct-write protein microfabrication.
机译:我们报告使用廉价,小型和“交钥匙”调Q 532 nm Nd:YAG激光器作为非线性,直接写入蛋白质微加工的来源。在这种方法中,使用高数值孔径光学器件将微焦耳脉冲(脉冲宽度,约600 ps)聚焦到亚微米焦点,从而产生足够大的瞬时强度,以促进光敏剂的多光子激发和随后的蛋白质分子间分子交联。通过用试剂溶液扫描飞升的聚焦体积,可以使用精确的三维形貌制造扩展的基于蛋白质的结构。与早期使用飞秒钛:蓝宝石激光器花费超过10万美元的研究一样,可以以小于0.5μm的特征尺寸快速形成物理坚固且具有化学响应性的微结构,并且可以使用两种生物良性敏化剂实现交联(例如黄素),并通过使用蛋白质本身来敏化交联。我们展示了原位制造的珊瑚神经突增生,并展示了利用生物素化试剂功能化抗生物素蛋白结构的能力,这种方法能够在特定的微环境中进行化学传感。这种廉价,低功耗的特性将大大拓宽直接写入蛋白质微加工的途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号