Construction of a new polycistronic vector for over-expression and rapid purification of human hemoglobin.

Abstract:

:To facilitate the study of the structure-function relationship of human hemoglobin (Hb A), we have developed a new hemoglobin expression vector, pGEX6P-alpha-[SD]-beta. This vector allows the co-expression of alpha-Hb as a fusion protein with Glutathione S-Transferase (GST-alpha-Hb) and beta-Hb with an additional methionine at the N-terminal extremity (rbeta-Hb). These proteins were solubilized as GST-alpha-Hb/rbeta-Hb complex form and purified in one step by affinity chromatography on immobilized glutathione. The CO binding kinetic studies show that the GST-alpha-Hb/rbeta-Hb complex and recombinant Hb A exhibit the same allosteric behavior as for native Hb A. The GST moiety, which does not modify the function of the complex, can be easily eliminated by cleavage by the PreScission Protease. After cleavage during the rapid purification procedure, over 20mg of recombinant Hb per liter of culture were obtained, more than double the yield of previous co-expression systems. This polycistronic vector system, which offers the additional advantage of a very rapid purification, is especially well suited for the study of abnormal, unstable globins in order to better understand the associated pathology.

journal_name

Plasmid

journal_title

Plasmid

authors

Domingues E,Brillet T,Vasseur C,Agier V,Marden MC,Baudin-Creuza V

doi

10.1016/j.plasmid.2008.09.006

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

71-7

issue

1

eissn

0147-619X

issn

1095-9890

pii

S0147-619X(08)00086-3

journal_volume

61

pub_type

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