Expression in Escherichia coli of chemically synthesized genes for human insulin.

Abstract:

:Synthetic genes for human insulin A and B chains were cloned separately in plasmid pBR322. The cloned synthetic genes were then fused to an Escherichia coli beta-galactosidase gene to provide efficient transcription and translation and a stable precursor protein. The insulin peptides were cleaved from beta-galactosidase, detected by radioimmunoassay, and purified. Complete purification of the A chain and partial purification of the B chain were achieved. These products were mixed, reduced, and reoxidized. The presence of insulin was detected by radioimmunoassay.

authors

Goeddel DV,Kleid DG,Bolivar F,Heyneker HL,Yansura DG,Crea R,Hirose T,Kraszewski A,Itakura K,Riggs AD

doi

10.1073/pnas.76.1.106

subject

Has Abstract

pub_date

1979-01-01 00:00:00

pages

106-10

issue

1

eissn

0027-8424

issn

1091-6490

journal_volume

76

pub_type

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