scholarly journals Protein engineering of antibody binding sites: recovery of specific activity in an anti-digoxin single-chain Fv analogue produced in Escherichia coli.

1988 ◽  
Vol 85 (16) ◽  
pp. 5879-5883 ◽  
Author(s):  
J. S. Huston ◽  
D. Levinson ◽  
M. Mudgett-Hunter ◽  
M. S. Tai ◽  
J. Novotny ◽  
...  
1991 ◽  
Vol 10 (6) ◽  
pp. 669-683 ◽  
Author(s):  
John E. McCartney ◽  
Lynne Lederman ◽  
Eric A. Drier ◽  
Nancy A. Cabral-Denison ◽  
Gay-May Wu ◽  
...  

FEBS Letters ◽  
1998 ◽  
Vol 425 (3) ◽  
pp. 479-484 ◽  
Author(s):  
Lynne J. Lawrence ◽  
Alexander A. Kortt ◽  
Peter Iliades ◽  
Peter A. Tulloch ◽  
Peter J. Hudson

2002 ◽  
Vol 26 (2) ◽  
pp. 218-228 ◽  
Author(s):  
Zhong Zhang ◽  
Zhi-Hua Li ◽  
Fei Wang ◽  
Min Fang ◽  
Chang-Cheng Yin ◽  
...  

2000 ◽  
Vol 66 (11) ◽  
pp. 5024-5029 ◽  
Author(s):  
Luis A. Fernández ◽  
Isabel Sola ◽  
Luis Enjuanes ◽  
Víctor de Lorenzo

ABSTRACT A simple method for the nontoxic, specific, and efficient secretion of active single-chain Fv antibodies (scFvs) into the supernatants ofEscherichia coli cultures is reported. The method is based on the well-characterized hemolysin transport system (Hly) of E. coli that specifically secretes the target protein from the bacterial cytoplasm into the extracellular medium without a periplasmic intermediate. The culture media that accumulate these Hly-secreted scFv's can be used in a variety of immunoassays without purification. In addition, these culture supernatants are stable over long periods of time and can be handled basically as immune sera.


2003 ◽  
Vol 77 (24) ◽  
pp. 13396-13398 ◽  
Author(s):  
Esteban Veiga ◽  
Víctor de Lorenzo ◽  
Luis Angel Fernández

ABSTRACT We report here that fusions of single-chain antibodies (scFvs) to the autotransporter β domain of the IgA protease of Neisseria gonorrhoeae are instrumental in locating virus-neutralizing activity on the cell surface of Escherichia coli. E. coli cells displaying scFvs against the transmissible gastroenteritis coronavirus on their surface blocked in vivo the access of the infectious agent to cultured epithelial cells. This result raises prospects for antiviral strategies aimed at hindering the entry into target cells by bacteria that naturally colonize the same intestinal niches.


1980 ◽  
Vol 26 (6) ◽  
pp. 718-723
Author(s):  
F H Verhoff ◽  
P J Lisi ◽  
C D Fischer ◽  
J W Teipel ◽  
G Goldstein ◽  
...  

Abstract A graphical procedure for determining the specific activity of radiolabeled ligands has been developed for use with radioimmunoassays. Although with this procedure we utilize the same experimental information required for displacement analysis, we are also able to determine both the specific activity and the binding constants of the labeled and unlabeled materials without assuming that these constants are equal; the concentration of antibody-binding sites can also be calculated. Thus, this graphical technique permits calculation of additional information without additional experimentation. We applied this procedure to the labeled materials used in a thymopoietin assay, testing two different preparations of radiolabeled material, and saw negligible differences between the two. The specific activity determined from the displacement analysis correlated well with that calculated by the graphical procedure.


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