TY - JOUR
T1 - Expression of caltrin in the baculovirus system and its purification in high yield and purity by cobalt (II) affinity chromatography
AU - Phan, Tony
AU - Nowak, Kristen
AU - Akkari, P.A.
AU - Zheng, Ming
AU - Xu, Jiake
PY - 2003
Y1 - 2003
N2 - Direct protein extraction from animals is the only approach available to obtain caltrin, calcium transport inhibitor. Here we report the expression and purification of caltrin, previously shown to hinder the influx of calcium into epididymal spermatozoa. Cloning of the caltrin gene into the pCDNA3.1 V5/His-TOPO vector and the subsequent ligation of the caltrin-His sequence into the transfer vector pBacPAK9 allowed the expression of recombinant caltrin using the baculovirus expression vector system (BEVS). Recombinant His-tagged caltrin was purified utilising both nickel (II)-nitrilotriacetic acid (Ni2+-NTA) and cobalt (II)-carboxymethylaspartate (CO2+-CmAsp) immobilised metal affinity chromatography (IMAC). Using the BEVS, caltrin-His was identified in the supernatant and in the cell lysate, suggesting that caltrin is a secreted protein. Based on sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blot results, purified recombinant caltrin-His was ascertained to be approximately 14.5 kDa. Purification under the Co2+ system yielded significantly purer protein samples when compared to the Ni2+ system. Furthermore, Co2+ was observed to bind the recombinant caltrin-His protein with higher efficiency and specificity and to yield a higher total protein concentration. Collectively, our results indicate that the Co2+ system would be a better approach for purifying caltrin-His proteins than the Ni2+. (C) 2003 Elsevier Science (USA). All rights reserved.
AB - Direct protein extraction from animals is the only approach available to obtain caltrin, calcium transport inhibitor. Here we report the expression and purification of caltrin, previously shown to hinder the influx of calcium into epididymal spermatozoa. Cloning of the caltrin gene into the pCDNA3.1 V5/His-TOPO vector and the subsequent ligation of the caltrin-His sequence into the transfer vector pBacPAK9 allowed the expression of recombinant caltrin using the baculovirus expression vector system (BEVS). Recombinant His-tagged caltrin was purified utilising both nickel (II)-nitrilotriacetic acid (Ni2+-NTA) and cobalt (II)-carboxymethylaspartate (CO2+-CmAsp) immobilised metal affinity chromatography (IMAC). Using the BEVS, caltrin-His was identified in the supernatant and in the cell lysate, suggesting that caltrin is a secreted protein. Based on sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blot results, purified recombinant caltrin-His was ascertained to be approximately 14.5 kDa. Purification under the Co2+ system yielded significantly purer protein samples when compared to the Ni2+ system. Furthermore, Co2+ was observed to bind the recombinant caltrin-His protein with higher efficiency and specificity and to yield a higher total protein concentration. Collectively, our results indicate that the Co2+ system would be a better approach for purifying caltrin-His proteins than the Ni2+. (C) 2003 Elsevier Science (USA). All rights reserved.
U2 - 10.1016/S1046-5928(03)00021-4
DO - 10.1016/S1046-5928(03)00021-4
M3 - Article
SN - 1046-5928
VL - 29
SP - 284
EP - 290
JO - Protein Expression and Purification
JF - Protein Expression and Purification
IS - 2
ER -