Rapid purification following enzyme-catalyzed nucleic acid reactions

描述（由申请人提供）：用于DNA分析和操作的生化反应对于许多应用都很重要，包括法医学，诊断基因测试和生物医学研究。将DNA切割并插入克隆位点的酶促反应是疾病研究和利用微生物表达具有医学价值的重要蛋白质的许多策略的基础。纯化以获得所需的反应组分，同时丢弃那些可能干扰DNA进一步使用的组分是必不可少的，并且对基因组学所涉及的时间，成本和劳动力做出了重大贡献。改进工作流程和实现下一代测序库生成过程中清理步骤的自动化，将消除令人兴奋和有前途的基因组图谱技术的一个瓶颈。Diffinity Genomics已经获得了在罗切斯特大学PI实验室开发的新材料技术的许可，该技术可用于纯化核酸反应所需的快速、廉价和简单的生物分子分离。特别是，Diffinity已经发布了一种产品，可以在测序反应之前进行聚合酶链扩增后快速，有效地纯化DNA。本提案中的工作涉及调整该技术以制造用于酶反应快速纯化的产品。目前纯化这些反应的方法需要多个步骤，并使用试剂将溶液中的所有生物分子结合到底物上，然后选择性地重新溶解所需的成分。Diffinity的净化方法是独特的，因为它使用特殊配置的表面，吸引溶液中不需要的成分，而将需要的成分留在溶液中。这使得可以通过在移液管尖端保留具有特殊功能化表面的颗粒来实现单步过程，从而使纯化过程简化为简单地吸入反应溶液并分配纯化的DNA反应溶液。我们将建立在我们成功的初步结果商业化一步，60秒的酶反应纯化产品。

DESCRIPTION (provided by applicant): Biochemical reactions used in the analysis and manipulation of DNA are important for many applications including forensics, diagnostic genetic testing and biomedical research. Enzymatic reactions to cut and insert DNA into cloning sites underpin many strategies for disease research and for use of microorganisms to express important proteins with medical value. Purification to obtain the desired reaction components while discarding those that can interfere with further use of the DNA is essential and comprises a significant contribution to the time, cost and labor involved in genomics. Improving workflow and enabling automation in the cleanup steps during library generation for next generation sequencing would remove one of the bottlenecks in that exciting and promising technology for genomic mapping. Diffinity Genomics has licensed novel materials technology developed in the PI's lab at the University of Rochester that can be used for fast, inexpensive and simple biomolecular separations needed to purify nucleic acid reactions. In particular, Diffinity has released a product enabling rapid, efficient purification of DNA after polymerase chain amplification prior to sequencing reactions. The work in the present proposal involves adapting that technology to make products for rapid purification of enzymatic reactions. Current approaches to purifying these reactions require multiple steps and use reagents to bind all of the biomolecules in solution to a substrate and then selectively redissolve the desired component. Diffinity's purification method is distinct because it uses specially configured surfaces that attract undesired components of a solution while leaving the desired ones in solution. This enables a single-step process that can be implemented by retaining particles with the specially functionalized surfaces in pipette tips so that the purification process is reduced simply to aspirating the reaction solution and dispensing the purified DNA reaction solution. We will build on our successful preliminary results to commercialize a single-step, 60 second enzymatic reaction purification product.