1 / 75

Prof. Fuad Fares University of Haifa

Developing long acting agonists and antagonists of glycoprotein hormones using gene fusion and gene transfer: from bench to clinics. Prof. Fuad Fares University of Haifa. 2 nd International conference on Endocrinology Chicago October 2014. Structure-Function studies

Download Presentation

Prof. Fuad Fares University of Haifa

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Developing long acting agonists and antagonists of glycoprotein hormones using gene fusion and gene transfer: from bench to clinics Prof. Fuad Fares University of Haifa 2nd International conference on Endocrinology Chicago October 2014

  2. Structure-Function studies Using site-directed mutagenesis and gene transfer Development of new analogs

  3. Therapeutical Recombinant proteins 1978 Human Growth Hormone 1979 Human Insulin

  4. The Problem Most therapeutic proteins are <30 kD and hence: • Are filtered out quickly by the kidneys • Are taken up by the liver and cleaved enzymatically • Have to be injected frequently for optimal therapy • Cause adverse effects due to peak dose injection

  5. Success of Long-Lasting Proteins • PEGylation - Interferon  (SGP/Roche) • PEGIntron/Pegasys • $3.2 billion in sales in 2006 • PEGylation - GCSF (Amgen) • Neulasta • $2.5 billion in sales in 2006 • Hyper Glycosylation- EPO (Amgen) • Aranesp (DNA Modifications) • $3.9 billion in sales in 2006

  6. Structure-Function of Glycoprotein Hormones FSH - Human Stimulating Hormone LH - Luteinizing Hormone hCG - Human Chorionic Gonadotropin TSH - Thyrotropin Hormone

  7. hCG hTSH

  8. Glycoprotein Hormone Subunits N N  N N hFSH N hLH N hTSH O-linked N N hCG CTP

  9. The Technology was Created By Nature During Evolution - the CTP “cassette” CTP A Two fertility hormones B hCG – maintains pregnancy and requires long T1/2 hCG C hLH – stimulates ovulation on a pulse mode requiring a short T1/2 D Amino acid sequence of hCG & hLH is almost identical hLH E The 28 amino acid C-terminal peptide (CTP) of hCG with its 4 O-glycans does not exist in hLH T1/2 of hCG is ~5 times longer than T1/2 of LH

  10. SerSerSerSerLysAlaProProProSerLeuProSerProSerArgLeu Pro GlyProSerAspThrProIleLeuProGln O O O O CTP

  11. Prediction of Folded and Unfolded Region of human chorionic gonadotropin (HCG) - chain B

  12. Crystal Structure of hGCβ showing long C-term lacking CTP N-terminal CTP not seen in structure

  13. N N  N N hCG TGA Stop Codon N N Mutated hCG N N The Role of CTP

  14. Deletion of CTP from hCG • No effect on the assembly of subunits • No effect on receptor binding • No effect on in vitro bioactivity - Significantly decreased the bioactivity in vivo

  15. + + Protein CTP Half- Life

  16. Designing New FSH Analog

  17. hCG Gene CTP hFSH Gene CTP Designing New FSH Analog hFSH Gene

  18. hFSH - CTP a Exon 2 a Exon 3 a Exon 4 NH2 COOH CTP FSHb Exon3 FSHb Exon 1 FSHb Exon 2 COOH NH2 1- Assembly of the subunits 2- Binding to the receptor 3- In vitro Bioactivity 4- In vivo Bioactivity 5- Immunogenecity

  19. Gene Expression  FSH -CTP Transfection CHO Stable Clone

  20. Assembly of Subunits hFSH-WT hFSH-CTP hFSH-(CTP)2 L M L M L M

  21. in vitro Studies

  22. 10 IU / 24h x 48h (IP) Estrogen (pg/ml) Control FSH-CTP FSH-WT

  23. 4/4 3/3 50 40 4/4 30 Number of ovulated oocytes 20 0/4 0/4 0/4 10 0 WT 1X 10 IU WT 4X 2.5IU C 1 3 10

  24. Half - Life

  25. SerSerSerSerLysAlaProProProSerLeuProSerProSerArgLeu Pro GlyProSerAspThrProIleLeuProGln O O O O CTP

  26. FSH -CTP Transfection into LDLD Cells

  27. Biological Activity E2Production(ng/ml) CHO Idl-D 50 40 30 20 10 0 FSH-CTP FSH-WT FSH-CTP

  28. SerSerSerSerLysAlaProProProSerLeuProSerProSerArgLeu Pro GlyProSerAspThrProIleLeuProGln O CTP O O O

  29. HumanStudies Organon - Merck • FSH – CTP is effective in follicular stimulation • FSH – CTP is safe • FSH – CTP is not immunogenic

  30. February 2, 2010 — The European Commission (EC) has approved ELONVA (FSH-CTP) Merck Receives Positive Regulatory Opinion for European Marketing of Long-Acting CTP-Modified Fertility Treatment ELONVA

  31. FSH – CTP(ELONVA) World – Wide Use

  32. Start Up Company CTP “Enhancing the potency and longevity of highly valuable proteins”

  33. Start Up Company Public Company • NASDAQ, Stock Exchange, NY, USA. • Tel-Aviv Stock Exchange, Tel-Aviv, Israel.

  34. OPKO Health, Inc. a multinational biopharmaceutical and diagnostics company

  35. Designing Long Acting Proteins Erythropoietin Growth Hormone Interferon Factors, XI & VII Short Peptides

  36. Erythropoietin (EPO) The most common use is in people with anemia (low blood count) related to kidney dysfunction.

  37. C-term N-term 3 - D Structure Analysis Human Erythropoietin  (blue) with its Receptors (cyan) Conclusion: Strands of both termini are fairly long and accessible.

  38. Xba I Not I 5’ - - 3’ CTP EPO - cDNA CTP CTP ATGGGGGTG….GGGGACAGA Met Gly Val….Gly Asp Arg 1 2 3 …. 190 191 192 TCCTCTTCC…..CTCCCACAATAA Ser Ser Ser …. Leu Pro Gln Term 118 119 120 …. 143 144 145 EPO-cDNA hCG-CTP Human EPO-CTP3

  39. 57 EPO (CTP)3 EPO - WT 37 28 Human EPO-CTP3

  40. 40 Control rhEPO 3 x week 30 EPO-(CTP)3 rhEPO 1 x week 20 Haematocrite (change from baseline, %) 10 Days Human EPO-CTP3

  41. rhEPO EPO – (CTP)3 AARANESP Human EPO-CTP3 Erythropoietin (mU/ml) Time (hours)

  42. Human Growth Hormone

  43. Pituitary

  44. Pharmaceutical and Biotechnological Uses of Growth Hormone To treat children of pathologically short stature

  45. C-term N-term 3-D Structure Analysis Human Growth Hormone (blue) with its Receptors (cyan) Conclusion: Both termini pointing away from the receptors and are accessible

  46. A. B. C. D. E. 4 1 2 TCCTCTTCC…..CTCCCACAATAA Ser Ser Ser …. Leu Pro Gln Term 118 119 120 …. 143 144 145 5' ATGGGGGTG….GGGGACAGA Met Gly Val….Gly Asp Arg 1 2 3 …. 190 191 192 '3 3 AgeI BamHI GH CTP GH-cDNA CG-CTP GH CTP CTP GH CTP CTP CTP CTP GH CTP GH CTP Fig.1.

  47. Secretion of GH Analogs from CHO cells

More Related