High yield production of recombinant native and modified peptides exemplified by ligands for G-protein coupled receptors

被引:33
|
作者
Bosse-Doenecke, Eva [1 ]
Weininger, Ulrich [2 ]
Gopalswamy, Mohanraj [2 ]
Balbach, Jochen [2 ,3 ]
Knudsen, Sanne Moller [4 ]
Rudolph, Rainer [1 ,3 ]
机构
[1] Univ Halle Wittenberg, Inst Biochem & Biotechnol, D-06120 Halle, Germany
[2] Univ Halle Wittenberg, Inst Phys, D-06099 Halle, Germany
[3] Univ Halle Wittenberg, Mitteldeutsch Zentrum Struktur & Dynam Prot, D-4010 Halle, Germany
[4] Novo Nordisk AS, DK-2760 Malov, Denmark
关键词
peptide expression; isotopic labelling; SUMO fusion protein; SUMO protease; g-protein coupled receptor; GLP-1; glucagon like peptide-1; receptor; PTH; parathyroid hormone; PTH receptor 1;
D O I
10.1016/j.pep.2007.10.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
G-protein coupled receptors (GPCRs) comprise a large family of membrane proteins and attract pharmaceutical interest as therapeutic targets. Two examples of class B GPCRs that are involved in metabolic diseases are the Parathyroid hormone receptor I (PTHR1) and the Glucagon-like-peptide-1 receptor (GLP-1R) which play central roles in osteoporosis and diabetes mellitus type 11, respectively. Class B GPCRs are characterised by a large extracellular N-terminal domain with a typical disulfide bridge pattern. This domain is responsible for the binding of peptide hormone ligands. Here we report the recombinant expression of these ligands in natural and several modified forms for their use in functional assays, NMR analyses or affinity purification of receptor/ligand complexes for crystallisation. Applying the SUMO system, low cost expression of soluble fusion-proteins is achieved. Moreover, via the SUMO cleavage site, the authentic N-terminal sequence which is essential for ligand receptor interactions can be obtained. Purification of the peptide by RP-HPLC results in > 98% pure preparations. The strategy can also be adopted for many other purposes, especially if small peptides are needed at either large amounts or with specific features like isotope, affinity or fluorescent labels. Furthermore, for the growing demand for therapeutic peptides, this method could represent a straightforward production process. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:114 / 121
页数:8
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