Rodriguez Camargo Diana C, Tripsianes Konstantinos, Kapp Tobias G, Mendes Joaquim, Schubert Jasmin, Cordes Burghard, Reif Bernd
Helmholtz Zentrum München (Deutsches Forschungszentrum für Gesundheit und Umwelt), Ingolstädter Landstr. 1, 85764 Neuherberg, Germany; Munich Center for Integrated Protein Science (CIPS-M) at Department Chemie, Technische Universität München (TUM), Lichtenbergstr. 4, 85747 Garching, Germany.
Central European Institute of Technology (CEITEC), Masaryk University, Kamenice 5/A35/1S081, 62500 Brno, Czech Republic.
Protein Expr Purif. 2015 Feb;106:49-56. doi: 10.1016/j.pep.2014.10.012. Epub 2014 Nov 6.
Type II diabetes is characterized by deposition of the hormone human Islet Amyloid Polypeptide (hIAPP). Formation of hIAPP amyloid fibrils and aggregates is considered to be responsible for pancreatic β-cell losses. Therefore, insight into the structure of hIAPP in the solid-state and in solution is of fundamental importance in order to better understand the action of small molecules, which can potentially dissolve protein aggregates and modulate cell toxicity. So far, no procedure has been described that allows to obtain the native human IAPP peptide at high yields. We present here a cloning, expression and purification protocol that permits the production of 2.5 and 3mg of native peptide per liter of minimal and LB medium, respectively. In the construct, hIAPP is fused to a chitin binding domain (CBD). The CBD is subsequently cleaved off making use of intein splicing reaction which yield amidation of the C-terminus. The N-terminus contains a solubilization domain which is cleaved by V8 protease, avoiding additional residues at the N-terminus. The correct formation of the disulfide bond is achieved by oxidation with H2O2.
2型糖尿病的特征是激素人胰岛淀粉样多肽(hIAPP)的沉积。hIAPP淀粉样纤维和聚集体的形成被认为是胰腺β细胞损失的原因。因此,深入了解固态和溶液状态下hIAPP的结构对于更好地理解小分子的作用至关重要,这些小分子可能溶解蛋白质聚集体并调节细胞毒性。到目前为止,尚未描述能够高产量获得天然人IAPP肽的方法。我们在此展示一种克隆、表达和纯化方案,该方案分别允许在每升基本培养基和LB培养基中产生2.5毫克和3毫克的天然肽。在构建体中,hIAPP与几丁质结合结构域(CBD)融合。随后利用内含肽剪接反应切除CBD,该反应导致C末端酰胺化。N末端包含一个可被V8蛋白酶切割的增溶结构域,避免在N末端产生额外的残基。通过用H2O2氧化实现二硫键的正确形成。