Human proinsulin production in the milk of transgenic cattle

Author:

Monzani Paulo S.12ORCID,Sangalli Juliano R.3,Sampaio Rafael V.3,Guemra Samuel1,Zanin Renato4,Adona Paulo R.1,Berlingieri Maria A.1,Cunha‐Filho Luiz F. C.1,Mora‐ Ocampo Irma Y.5,Pirovani Carlos P.5,Meirelles Flávio V.2,Wheeler Matthew B.2ORCID,Ohashi Otavio M.6

Affiliation:

1. Center for Biological and Health Sciences University of Northern Paraná Londrina Paraná Brazil

2. Department of Animal Sciences University of Illinois at Urbana‐Champaign Urbana Illinois USA

3. Department of Veterinary Medicine University of São Paulo Pirassununga São Paulo Brazil

4. Laffranchi Agriculture Tamarana Paraná Brazil

5. Department of Biological Sciences State University of Santa Cruz (UESC) Ilhéus Bahia Brazil

6. Institute of Biological Sciences Federal University of Pará Belém Pará Brazil

Abstract

AbstractBackgroundThe worldwide growing demand for human insulin for treating diabetes could be supplied by transgenic animals producing insulin in their milk.Methods and ResultsPseudo‐lentivirus containing the bovine β‐casein promoter and human insulin sequences was used to produce modified adult fibroblasts, and the cells were used for nuclear transfer. Transgenic embryos were transferred to recipient cows, and one pregnancy was produced. Recombinant protein in milk was evaluated using western blotting and mass spectrometry. One transgenic cow was generated, and in milk analysis, two bands were observed in western blotting with a molecular mass corresponding to the proinsulin and insulin. The mass spectrometry analysis showed the presence of human insulin more than proinsulin in the milk, and it identified proteases in the transgenic milk that could convert proinsulin into insulin and insulin‐degrading enzyme that could degrade the recombinant protein.ConclusionThe methodologies used for generating the transgenic cow allowed the detection of the production of recombinant protein in the milk at low relative expression compared to milk proteins, using mass spectrometry, which was efficient for detecting recombinant protein with low expression in milk. Milk proteases could act on protein processing converting recombinant protein to functional protein. On the other hand, some milk proteases could act in degrading the recombinant protein.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

University of Illinois at Urbana-Champaign

U.S. Department of Agriculture

Publisher

Wiley

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