A composition for treating diabetes or diabesity comprising oxyntomodulin analog
a technology of oxyntomodulin and diabesity, which is applied in the direction of peptide/protein ingredients, extracellular fluid disorder, metabolic disorder, etc., can solve the problems of increasing the risk of retinopathy, neuropathy, neuropathy caused by vascular disorder, etc., and achieves high activity to activate, reduce blood glucose levels, and increase insulin secretion
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example 1-1
Production of Cell Line Showing cAMP Response to GLP-1
[0095]Using a portion corresponding to the ORF (open reading frame) of cDNA (OriGene Technologies, Inc. USA) of the human GLP-1 receptor gene as a template, PCR was performed using reverse and forward primers including a HindIII cleavage site and an EcoRI cleavage site, respectively, thereby obtaining a PCR product.
Forward primer:(SEQ ID NO: 50)5′-CCCGGCCCCCGCGGCCGCTATTCGAAATAC-3′Reverse primer:SEQ ID NO: 51)5′-GAACGGTCCGGAGGACGTCGACTCTTAAGATAG-3′
[0096]The PCR product was cloned into the known animal cell expression vector x0GC / dhfr, thereby constructing the recombinant vector x0GC / GLP-1R.
[0097]The recombinant vector x0GC / GLP-1R was introduced into a CHO DG44 cell line, cultured in DMEM / F12 (10% FBS) medium, using lipofectamine (Invitrogene, USA), to obtain a transformant. The transformant was incubated in a selective medium containing 1 mg / mL G418 and 10 nM methotraxate, and monoclonal cell lines were selected therefrom. Then, a...
example 1-2
Production of Cell Line Showing cAMP Response to Glucagon
[0098]Using a portion corresponding to the ORF (open reading frame) of cDNA (OriGene Technologies, Inc. USA) of the human glucagon receptor gene as a template, PCR was performed using reverse and forward primers including an EcoRI cleavage site and a XhoI cleavage site, respectively, thereby obtaining a PCR product.
Forward primer:(SEQ ID NO: 52)5′-CAGCGACACCGACCGTCCCCCCGTACTTAAGGCC-3′Reverse Primer:(SEQ ID NO: 53)5′-CTAACCGACTCTCGGGGAAGACTGAGCTCGCC-3′
[0099]The PCR product was cloned into the known animal cell expression vector x0GC / dhfr, thereby constructing the recombinant vector x0GC / GCGR.
[0100]The recombinant vector x0GC / GCGR was introduced into a CHO DG44 cell line, cultured in DMEM / F12 (10% FBS) medium, using lipofectamine (Invitrogene, USA), to obtain a transformant. The transformant was incubated in a selective medium containing 1 mg / mL G418 and 10 nM methotraxate, and monoclonal cell lines were selected therefrom. Then...
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