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钙在大鼠皮层中区分出两个具有不同分子靶点大小的[3H]海人酸结合位点。

Calcium discriminates two [3H]kainate binding sites with different molecular target sizes in rat cortex.

作者信息

Honoré T, Drejer J, Nielsen M

出版信息

Neurosci Lett. 1986 Mar 28;65(1):47-52. doi: 10.1016/0304-3940(86)90118-7.

Abstract

Binding of [3H]kainate to the kainate subtype of excitatory amino acid receptors revealed two binding sites. The high-affinity site (Kd = 3.5 nM) was sensitive to calcium ions and has a molecular target size as determined by high-energy radiation inactivation analysis of 76,600 daltons. The low-affinity site (Kd = 65 nM) was insensitive to calcium ions and has a molecular target size similar to the quisqualate-subtype of excitatory amino acid receptors. The change in binding parameters of the two sites with radiation dose strongly suggests that low affinity, calcium-insensitive [3H]kainate binding sites are equivalent to quisqualate sites.

摘要

[3H]海人酸与兴奋性氨基酸受体的海人酸亚型结合显示出两个结合位点。高亲和力位点(Kd = 3.5 nM)对钙离子敏感,通过高能辐射失活分析确定其分子靶标大小为76,600道尔顿。低亲和力位点(Kd = 65 nM)对钙离子不敏感,其分子靶标大小与兴奋性氨基酸受体的quisqualate亚型相似。两个位点的结合参数随辐射剂量的变化强烈表明,低亲和力、对钙不敏感的[3H]海人酸结合位点等同于quisqualate位点。

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