Rodríguez de la Vega Ricardo C, Merino Enrique, Becerril Baltazar, Possani Lourival D
Institute of Biotechnology, National Autonomous University of Mexico, Avenida Universidad, 2001, Apartado Postal 510-3, Cuernavaca 62210, Mexico.
Trends Pharmacol Sci. 2003 May;24(5):222-7. doi: 10.1016/S0165-6147(03)00080-4.
K(+) channels are macromolecules embedded in biological membranes, where they play a key role in cellular excitability and signal transduction pathways. Knowledge of their structure should help improve our understanding of their function and lead to the design of therapeutic compounds. Most pharmacological and structural characteristics of these channels have been elucidated by using high-affinity channel blockers isolated from scorpion venoms. Recent data on the three-dimensional structures of K(+) channels and novel scorpion toxins suggest a variety of novel interacting modes of these channels and toxins, which should help increase our understanding of the K(+) channel structure-function relationship.
钾离子通道是嵌入生物膜中的大分子,在细胞兴奋性和信号转导途径中发挥关键作用。了解其结构应有助于增进我们对其功能的理解,并推动治疗性化合物的设计。这些通道的大多数药理学和结构特征已通过使用从蝎毒中分离出的高亲和力通道阻滞剂得以阐明。关于钾离子通道三维结构和新型蝎毒素的最新数据表明,这些通道和毒素存在多种新型相互作用模式,这应有助于加深我们对钾离子通道结构与功能关系的理解。