TY - CHAP
T1 - Preparation of temperature-sensitive antibody fragments
AU - Kamihira, Masamichi
AU - Iijima, Shinji
PY - 2000
Y1 - 2000
N2 - We designed a temperature-sensitive single chain, antibody fragment in which the antigen-binding activity was drastically altered by a temperature-shift between 4 and 37°C. An oligonucleotide corresponding to the temperature-sensitive helix-coil transition peptide,-(-Glu Ala Ala Ala Lys-)-, was introduced between Vh and Vl genes of scFv against the simian virus 40 large T antigen. The antigen-binding activity of the temperature-sensitive scFv produced by Escherichia coli cells showed a maximum decrease of 1/36 at 4°C compared with that at 37°C. Binding activity was controlled by the NaCl concentration, as well as by the temperature shift. By using a column that immobilized the ScFv, the antigen was purified in response to elution by the temperature-shift.
AB - We designed a temperature-sensitive single chain, antibody fragment in which the antigen-binding activity was drastically altered by a temperature-shift between 4 and 37°C. An oligonucleotide corresponding to the temperature-sensitive helix-coil transition peptide,-(-Glu Ala Ala Ala Lys-)-, was introduced between Vh and Vl genes of scFv against the simian virus 40 large T antigen. The antigen-binding activity of the temperature-sensitive scFv produced by Escherichia coli cells showed a maximum decrease of 1/36 at 4°C compared with that at 37°C. Binding activity was controlled by the NaCl concentration, as well as by the temperature shift. By using a column that immobilized the ScFv, the antigen was purified in response to elution by the temperature-shift.
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U2 - 10.1016/S0921-0423(00)80027-1
DO - 10.1016/S0921-0423(00)80027-1
M3 - Chapter
AN - SCOPUS:77957047905
T3 - Progress in Biotechnology
SP - 143
EP - 148
BT - Progress in Biotechnology
PB - Elsevier
ER -