Department of Cardiovascular and Metabolic Diseases, Wyeth Research, Cambridge, Massachusetts, 02140, USA,
Purinergic Signal. 2006 Jun;2(2):327-33. doi: 10.1007/s11302-005-5300-7. Epub 2006 Jun 1.
It has long been known that the salivary glands of hematophagous (blood-feeding) arthropods secrete soluble apyrases, which are potent nucleotide hydrolyzing enzymes capable of hydrolyzing extracellular ATP and ADP, the latter being a major agonist contributing to platelet aggregation. Only recently, however, has the identification of proteins homologous to these apyrases been reported in non-blood-feeding organisms such as rodents and humans. In this review, we present an overview of the diverse family of apyrases first described in the blood-feeding arthropods, including the identification and characterization of the soluble and membrane-bound vertebrate enzymes homologous to these arthropod apyrases. We also describe the enzymatic properties and nucleotide specificities of the expressed enzymes, and insights gained into the structure and function of this calcium activated nucleotidase (CAN) family from biophysical, mutagenesis and crystallography studies. The potential therapeutic value of these proteins is also discussed.
长期以来,人们一直知道吸血节肢动物的唾液腺会分泌可溶性的apyrases,这是一种能够水解细胞外 ATP 和 ADP 的强效核苷酸水解酶,ADP 是导致血小板聚集的主要激动剂。然而,直到最近,在非吸血生物(如啮齿动物和人类)中才发现与这些 apyrases 同源的蛋白质。在这篇综述中,我们首先概述了在吸血节肢动物中首次描述的 apyrase 家族,包括对与这些节肢动物 apyrases 同源的可溶性和膜结合的脊椎动物酶的鉴定和特性描述。我们还描述了表达酶的酶学特性和核苷酸特异性,并通过生物物理、突变和晶体学研究深入了解了这种钙激活核苷酸酶 (CAN) 家族的结构和功能。还讨论了这些蛋白质的潜在治疗价值。