Malik K F, Young W S
Laboratory of Cell Biology, NIMH, NIH, Bethesda, Maryland 20892, USA.
Endocrinology. 1996 Apr;137(4):1497-500. doi: 10.1210/endo.137.4.8625929.
Leptin (OB protein) fused to the FLAG epitope and a kinase recognition site was expressed in bacteria, immunopurified, and phosphorylated using [gamma-(33)P] ATP. The resulting probe was used to characterize the distribution of leptin binding sites within brain sections of normal, ob/ob, and db/db C57BL/6J male mice. Leptin binding sites were found in leptomeninges and choroid plexus. Leptin binding within the choroid plexus is slightly elevated in ob/ob mice when compared to normal males (p<0.05). Binding of leptin by the choroid plexus of db/db male mice is lower than in normal males (p<0.05), but normally distributed. Based on the association and dissociation rates of leptin binding on tissue sections, we estimate the K(D) of the choroid plexus site at 0.25X10(-9) M. From our results, we hypothesize that the binding of leptin to its site may cause the release or transport of uncharacterized factor(s) into the cerebral spinal fluid (CSF) to affect neuronal populations controlling feeding and metabolism.
与FLAG表位和激酶识别位点融合的瘦素(OB蛋白)在细菌中表达,经免疫纯化后,使用[γ-(33)P]ATP进行磷酸化。所得探针用于表征正常、ob/ob和db/db C57BL/6J雄性小鼠脑切片中瘦素结合位点的分布。在软脑膜和脉络丛中发现了瘦素结合位点。与正常雄性小鼠相比,ob/ob小鼠脉络丛中的瘦素结合略有升高(p<0.05)。db/db雄性小鼠脉络丛对瘦素的结合低于正常雄性小鼠(p<0.05),但呈正态分布。根据瘦素在组织切片上的结合和解离速率,我们估计脉络丛位点的K(D)为0.25×10(-9)M。根据我们的结果,我们推测瘦素与其位点的结合可能导致未表征因子释放或转运至脑脊液(CSF)中,从而影响控制进食和代谢的神经元群体。