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14-3-3ζ-GPIb-IX-V复合物作为抗血小板靶点。

The 14-3-3zeta-GPIb-IX-V complex as an antiplatelet target.

作者信息

Andrews Robert K, Du Xiaoping, Berndt Michael C

机构信息

Department of Immunology, Monash University, Melbourne, Australia.

出版信息

Drug News Perspect. 2007 Jun;20(5):285-92. doi: 10.1358/dnp.2007.20.5.1120215.

Abstract

The functional nexus involving the platelet adhesion receptor, the glycoprotein (GP)Ib-IX-V complex, and the signaling protein, 14-3-3zeta, is emerging as a new drug target for control of GPIb-IX-V-dependent thrombotic diseases such as heart attack and stroke. Together, advances in understanding mechanisms of regulation and functional consequences of the GPIb-IX-V/14-3-3zeta interaction, and the growing potential of 14-3-3-targeting therapeutic approaches used for 14-3-3-dependent processes in other cells--principally involving cell cycling and cancer--point to 14-3-3zeta as a promising antithrombotic target. The unique recognition sequences and arrangement of functional 14-3-3zeta-binding sites found within the cytoplasmic domain of GPIb-IX-V increase the likelihood of selective targeting of this interaction.

摘要

涉及血小板粘附受体、糖蛋白(GP)Ib-IX-V复合物和信号蛋白14-3-3ζ的功能联系,正成为控制如心脏病发作和中风等GPIb-IX-V依赖性血栓性疾病的新药物靶点。同时,在理解GPIb-IX-V/14-3-3ζ相互作用的调节机制和功能后果方面取得的进展,以及用于其他细胞中14-3-3依赖性过程(主要涉及细胞周期和癌症)的靶向14-3-3治疗方法的潜力不断增加,都表明14-3-3ζ是一个有前景的抗血栓靶点。在GPIb-IX-V胞质结构域内发现的功能性14-3-3ζ结合位点的独特识别序列和排列,增加了选择性靶向这种相互作用的可能性。

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