Roy, Satarupa and Setlur, Sunita and Gadkari, Rupali A and Krishnamurthy, HN and Dighe, Rajan R (2007) Translational fusion of two beta-subunits of human chorionic gonadotropin results in production of a novel antagonist of. In: Endocrinology, 148 (8). pp. 3977-3986.
3977.pdf - Published Version
Restricted to Registered users only
Download (461Kb) | Request a copy
The strategy of translationally fusing the alpha-and beta-subunits of human chorionic gonadotropin (hCG) into a single-chain molecule has been used to produce novel analogs of hCG. Previously we reported expression of a biologically active singlechain analog hCG alpha beta expressed using Pichia expression system. Using the same expression system, another analog, in which the alpha-subunit was replaced with the second beta-subunit, was expressed (hCG beta beta) and purified. hCG beta beta could bind to LH receptor with an affinity three times lower than that of hCG but failed to elicit any response. However, it could inhibit response to the hormone in vitro in a dose- dependent manner. Furthermore, it inhibited response to hCG in vivo indicating the antagonistic nature of the analog. However, it was unable inhibit human FSH binding or response to human FSH, indicating the specificity of the effect. Characterization of hCG alpha beta and hCG beta beta using immunological tools showed alterations in the conformation of some of the epitopes, whereas others were unaltered. Unlike hCG, hCG beta beta interacts with two LH receptor molecules. These studies demonstrate that the presence of the second beta-subunit in the single-chain molecule generated a structure that can be recognized by the receptor. However, due to the absence of alpha-subunit, the molecule is unable to elicit response. The strategy of fusing two beta-subunits of glycoprotein hormones can be used to produce antagonists of these hormones.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to Endocrine Society.|
|Department/Centre:||Division of Biological Sciences > Molecular Reproduction, Development & Genetics (formed by the merger of DBGL and CRBME)|
|Date Deposited:||09 Apr 2010 11:19|
|Last Modified:||19 Sep 2010 05:59|
Actions (login required)