PROLink-Single Step Circularization and Purification Procedure for the Generation of an Improved Variant of Human Growth Hormone

被引:11
|
作者
Rasche, Nicolas [1 ,2 ]
Tonillo, Jason [2 ]
Rieker, Marcel [1 ,2 ]
Becker, Stefan [2 ]
Dorr, Brent [5 ]
Ter-Ovanesyan, Dmitry [3 ,4 ]
Betz, Ulrich A. K. [2 ]
Hock, Bjoern [2 ]
Kolmar, Harald [1 ]
机构
[1] Tech Univ Darmstadt, Inst Organ Chem & Biochem, D-64287 Darmstadt, Germany
[2] Merck KGaA, Frankfurterstr 250, D-64293 Darmstadt, Germany
[3] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[4] Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[5] GlaxoSmithKline, Platform Technol & Sci, Prussia, PA 19406 USA
关键词
HALF-LIFE; BACKBONE CYCLIZATION; SORTASE; PROTEINS; STABILITY; PROLACTIN; RECEPTOR; PEPTIDE; PEGYLATION; CONOTOXIN;
D O I
10.1021/acs.bioconjchem.6b00137
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human growth hormone (hGH) plays an important role during human development and is also an approved therapeutic for the treatment of several diseases. However, one major drawback of hGH is its short circulating half-life requiring frequent administration, which is inconvenient and painful for the patients. Recent publications indicate that circularization greatly increases the stability of proteins due to their protection from exoproteolytic attack and a higher thermal stability of the circular form. Using sortase A, a transpeptidase isolated from Staphylococcus aureus, we developed a single step solid-phase circularization and purification procedure resulting in a circular version of hGH with improved properties. We could show that circular hGH binds to the recombinant hGH receptor with binding kinetics similar to those of linear hGH and that circularization does not alter the biological activity of hGH in vitro. Besides, circular hGH showed almost complete resistance toward exoproteolytic attack and slightly increased thermal stability which could possibly translate into an extended plasma half-life. The single step solid-phase circularization and purification procedure is in principle a generic process, which could also be applied for other proteins that meet the requirements for circularization.
引用
收藏
页码:1341 / 1347
页数:7
相关论文
共 5 条
  • [1] Purification of a recombinant human growth hormone by an integrated IMAC procedure
    Mooney, Jane T.
    Fredericks, Dale P.
    Zhang, Chunfang
    Christensen, Thorkild
    Jespergaard, Christina
    Schiodt, Christine Bruun
    Hearn, Milton T. W.
    PROTEIN EXPRESSION AND PURIFICATION, 2014, 94 : 85 - 94
  • [2] Single Step Recombinant Human Growth Hormone (rhGH) Purification from Milk by Peptide Affinity Chromatography
    Saavedra, Soledad L.
    Martinez Ceron, Maria C.
    Giudicessi, Silvana L.
    Forno, Guillermina
    Belen Bosco, Maria
    Marani, Mariela M.
    Erra-Balsells, Rosa
    Albericio, Fernando
    Cascone, Osvaldo
    Camperi, Silvia A.
    BIOTECHNOLOGY PROGRESS, 2018, 34 (04) : 999 - 1005
  • [3] Single chain Fc-dimer-human growth hormone fusion protein for improved drug delivery
    Zhou, Li
    Wang, Hsuan-Yao
    Tong, Shanshan
    Okamoto, Curtis T.
    Shen, Wei-Chiang
    Zaro, Jennica L.
    BIOMATERIALS, 2017, 117 : 24 - 31
  • [4] Optimization of immobilized metal ion affinity chromatography for single-step purification of recombinant ovine growth hormone expressed in Escherichia coli
    Gupta, V
    Eshwari, ANS
    Panda, AK
    Agarwal, GP
    JOURNAL OF CHROMATOGRAPHY A, 2003, 998 (1-2) : 93 - 101
  • [5] Soluble Expression, One-Step Purification and Characterization of Recombinant Human Growth Hormone Fused with ompA3 in Escherichia coli
    Zhou, Zhen-Ru
    Huang, Wei
    Liu, Kang-Jia
    Lin, Fo-Lan
    Wang, Xiao-Lu
    Wang, Feng
    Jiang, Ren-Wang
    PROTEIN AND PEPTIDE LETTERS, 2021, 28 (05) : 533 - 542