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Article type: Research Article
Authors: Lo, Kin-Ming; | Roy, Aparna; | Foley, Susan F. | Coll, Joyce T. | Gillies, Stephen D.
Affiliations: Abbott Biotech, Inc., Needham Heights, MA, USA
Note: [] Address reprint requests to Dr. Kin-Ming Lo at his present address, 840 Mayer, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
Note: [] Present address of Aparna Roy: BASF Bioresearch Corp., 195 Albany Street, Cambridge, MA 02139, USA.
Abstract: We have expressed in E. coli a functional assembled antibody variant that is secreted into the media. The antibody variant is a CH2-deleted chimeric antibody 14.18, which was previously shown to be a potentially useful reagent for radioimmunodetection of human tumors. The bacterial expression vector contains a dicistronic unit comprised of a L-chain cDNA and a CH2-deleted H-chain cDNA. For translocation across the bacterial membranes, we have replaced the natural signal peptides of the H and L chains with the signal peptide of the bacterial protein pectate lyase B. When expressed in the JM105 host under the control of the trp-lac promoter, the products were secreted into the M9 growth media to about 350 μgl/L. The secreted antibody, which can be readily purified from the media without any denaturation or renaturation steps, retains antigen-binding activity. SDS-PAGE and nondenaturing size exclusion high-pressure liquid chromatography showed that it is a mixture of assembled HL and fully assembled H2L2. In H2L2, inter-H chain disulfide bonds are not formed, and the two HL half-molecules are likely held together by the trans interaction between the two CH3 domains.
Keywords: bacterial expression, secretion, pelB leader, CH2-deleted antibody
DOI: 10.3233/HAB-1992-3302
Journal: Human Antibodies, vol. 3, no. 3, pp. 123-128, 1992
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