Tassa Carlos, Liong Monty, Hilderbrand Scott, Sandler Jason E, Reiner Thomas, Keliher Edmund J, Weissleder Ralph, Shaw Stanley Y
Center for Systems Biology, Massachusetts General Hospital.
J Vis Exp. 2013 Sep 23(79):e50772. doi: 10.3791/50772.
Methods for rapid surface immobilization of bioactive small molecules with control over orientation and immobilization density are highly desirable for biosensor and microarray applications. In this Study, we use a highly efficient covalent bioorthogonal [4+2] cycloaddition reaction between trans-cyclooctene (TCO) and 1,2,4,5-tetrazine (Tz) to enable the microfluidic immobilization of TCO/Tz-derivatized molecules. We monitor the process in real-time under continuous flow conditions using surface plasmon resonance (SPR). To enable reversible immobilization and extend the experimental range of the sensor surface, we combine a non-covalent antigen-antibody capture component with the cycloaddition reaction. By alternately presenting TCO or Tz moieties to the sensor surface, multiple capture-cycloaddition processes are now possible on one sensor surface for on-chip assembly and interaction studies of a variety of multi-component structures. We illustrate this method with two different immobilization experiments on a biosensor chip; a small molecule, AP1497 that binds FK506-binding protein 12 (FKBP12); and the same small molecule as part of an immobilized and in situ-functionalized nanoparticle.
对于生物传感器和微阵列应用而言,能够控制取向和固定密度来快速实现生物活性小分子表面固定的方法是非常理想的。在本研究中,我们利用反式环辛烯(TCO)与1,2,4,5-四嗪(Tz)之间高效的共价生物正交[4+2]环加成反应,实现TCO/Tz衍生化分子的微流控固定。我们使用表面等离子体共振(SPR)在连续流动条件下实时监测该过程。为了实现可逆固定并扩展传感器表面的实验范围,我们将非共价抗原-抗体捕获组件与环加成反应相结合。通过交替地将TCO或Tz部分呈现给传感器表面,现在可以在一个传感器表面上进行多个捕获-环加成过程,用于各种多组分结构的芯片上组装和相互作用研究。我们通过在生物传感器芯片上进行的两个不同固定实验来说明这种方法;一种与FK506结合蛋白12(FKBP12)结合的小分子AP1497;以及作为固定化且原位功能化纳米颗粒一部分的相同小分子。