Zhang Limin, Bhojani Mahaveer S, Ross Brian D, Rehemtulla Alnawaz
Department of Radiation Oncology, University of Michigan School of Medicine, Ann Arbor, Michigan 48109, USA.
Cell Cycle. 2008 Feb 1;7(3):314-7. doi: 10.4161/cc.7.3.5409. Epub 2007 Dec 3.
Protein kinases are important regulators of signal-transduction pathways. Dysregulated kinase activity is observed in a variety of human diseases such as cancer, making them targets for the development of molecular therapies. Identification of new drugs is greatly aided by molecular imaging tools which enable real time, non-invasive, dynamic and quantitative imaging of kinase activity in vivo. We have recently described a new reporter platform based on conformation dependent complementation of firefly luciferase to monitor serine/threonine kinase (Akt) activity. The reporter system provides unique insights into the pharmacokinetics and pharmacodynamics of drugs that modulate kinase activity in living subjects and also provide a platform for cell based high-throughput drug screening for modulators of kinase activity.
蛋白激酶是信号转导通路的重要调节因子。在多种人类疾病如癌症中都观察到激酶活性失调,这使其成为分子疗法开发的靶点。分子成像工具极大地辅助了新药的鉴定,这些工具能够对体内激酶活性进行实时、非侵入性、动态和定量成像。我们最近描述了一种基于萤火虫荧光素酶构象依赖性互补的新型报告平台,用于监测丝氨酸/苏氨酸激酶(Akt)活性。该报告系统为深入了解调节活体受试者激酶活性的药物的药代动力学和药效学提供了独特视角,也为基于细胞的激酶活性调节剂高通量药物筛选提供了一个平台。