TY - JOUR
T1 - Photocleavable linkage between genotype and phenotype for rapid and efficient recovery of nucleic acids encoding affinity-selected proteins
AU - Doi, Nobuhide
AU - Takashima, Hideaki
AU - Wada, Aiko
AU - Oishi, Yuko
AU - Nagano, Tetsuya
AU - Yanagawa, Hiroshi
N1 - Funding Information:
The authors thank members of our laboratory for experimental advice and useful discussions. This research was supported in part by the Industrial Technology Research Grant Program from the NEDO of Japan, by the Program for Promotion of Fundamental Studies in Health Sciences of the NIBIO of Japan, and by a Grant-in-Aid for Scientific Research from the MEXT of Japan.
PY - 2007/9/15
Y1 - 2007/9/15
N2 - In vitro display technologies, such as mRNA display and DNA display are powerful tools to screen peptides and proteins with desired functions from combinatorial libraries in the fields of directed protein evolution and proteomics. When screening combinatorial libraries of polypeptides (phenotype), each of which is displayed on its gene (genotype), the problem remains, how best to recover the genotype moiety whose phenotype moiety has bound to the desired target. Here, we describe the use of a photocleavable 2-nitrobenzyl linker between genotype (DNA or mRNA) and phenotype (protein) in our DNA and mRNA display systems. This technique allows rapid and efficient recovery of selected nucleic acids by simple UV irradiation at 4 °C for 15 min. Further, we confirmed that the photocleavable DNA display and mRNA display systems are useful for in vitro selection of epitope peptides, recombinant antibodies, and drug-receptor interactions. Thus, these improved methods should be useful in therapeutics and diagnostics, e.g., for screening high-affinity binders, such as enzyme inhibitors and recombinant antibodies from random peptide and antibody libraries, as well as for screening drug-protein interactions from cDNA libraries.
AB - In vitro display technologies, such as mRNA display and DNA display are powerful tools to screen peptides and proteins with desired functions from combinatorial libraries in the fields of directed protein evolution and proteomics. When screening combinatorial libraries of polypeptides (phenotype), each of which is displayed on its gene (genotype), the problem remains, how best to recover the genotype moiety whose phenotype moiety has bound to the desired target. Here, we describe the use of a photocleavable 2-nitrobenzyl linker between genotype (DNA or mRNA) and phenotype (protein) in our DNA and mRNA display systems. This technique allows rapid and efficient recovery of selected nucleic acids by simple UV irradiation at 4 °C for 15 min. Further, we confirmed that the photocleavable DNA display and mRNA display systems are useful for in vitro selection of epitope peptides, recombinant antibodies, and drug-receptor interactions. Thus, these improved methods should be useful in therapeutics and diagnostics, e.g., for screening high-affinity binders, such as enzyme inhibitors and recombinant antibodies from random peptide and antibody libraries, as well as for screening drug-protein interactions from cDNA libraries.
KW - Directed evolution
KW - Drug receptor
KW - Protein engineering
KW - Proteomics
KW - Puromycin
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U2 - 10.1016/j.jbiotec.2007.07.947
DO - 10.1016/j.jbiotec.2007.07.947
M3 - Article
C2 - 17767970
AN - SCOPUS:34548388477
SN - 0168-1656
VL - 131
SP - 231
EP - 239
JO - Journal of Biotechnology
JF - Journal of Biotechnology
IS - 3
ER -