Department of Mathematics, Natural and Computer Sciences, Hochschule Mittweida, University of Applied Sciences, Technikumplatz 17, 09648 Mittweida, Germany.
Comput Math Methods Med. 2012;2012:790281. doi: 10.1155/2012/790281. Epub 2012 Mar 15.
Diabetes insipidus (DI) is a rare endocrine, inheritable disorder with low incidences in an estimated one per 25,000-30,000 live births. This disease is characterized by polyuria and compensatory polydypsia. The diverse underlying causes of DI can be central defects, in which no functional arginine vasopressin (AVP) is released from the pituitary or can be a result of defects in the kidney (nephrogenic DI, NDI). NDI is a disorder in which patients are unable to concentrate their urine despite the presence of AVP. This antidiuretic hormone regulates the process of water reabsorption from the prourine that is formed in the kidney. It binds to its type-2 receptor (V2R) in the kidney induces a cAMP-driven cascade, which leads to the insertion of aquaporin-2 water channels into the apical membrane. Mutations in the genes of V2R and aquaporin-2 often lead to NDI. We investigated a structure model of V2R in its bound and unbound state regarding protein stability using a novel protein energy profile approach. Furthermore, these techniques were applied to the wild-type and selected mutations of aquaporin-2. We show that our results correspond well to experimental water ux analysis, which confirms the applicability of our theoretical approach to equivalent problems.
尿崩症(DI)是一种罕见的内分泌遗传疾病,估计每 25000-30000 例活产中就有一例。这种疾病的特征是多尿和代偿性多饮。DI 的不同潜在原因可能是中枢缺陷,即垂体不能释放功能性血管加压素(AVP),也可能是肾脏缺陷的结果(肾性尿崩症,NDI)。NDI 是一种尽管存在 AVP,但患者仍无法浓缩尿液的疾病。这种抗利尿激素调节了从肾脏形成的原尿中重吸收水分的过程。它与肾脏中的 2 型受体(V2R)结合,诱导 cAMP 驱动的级联反应,导致水通道蛋白-2 水通道插入顶端膜。V2R 和水通道蛋白-2 的基因突变常导致 NDI。我们使用一种新的蛋白质能量谱方法研究了 V2R 在结合和未结合状态下的结构模型,以评估其蛋白质稳定性。此外,这些技术还应用于水通道蛋白-2 的野生型和选定突变体。我们的结果与实验水通量分析非常吻合,这证实了我们的理论方法在等效问题上的适用性。