Characterization of the optimized C2 domain of protein G: finding its additional chicken IgY-binding ability
Abstract The C2 domain of streptococcal protein G is a small (55 residue) peptide with immunoglobulin-binding activity. Following codon optimization, the gene was divided into four oligonucleotide fragments and amplified by overlap PCR. The recombinant plasmid pET30a-C2 was transformed into Escherichia coli Rosetta (DE3) PLysS for expression. After purification by Ni–NTA, the fusion protein was identified by western-blotting, Dot-ELISA and ELISA. His-tagged C2 bound to human, rabbit, cattle, pig, goat, mouse or guinea pig IgG had no affinity for goose, duck, wild duck, wild turkey and red-crowned crane IgY. Its affinity for chicken IgY, however, was comparable to that of guinea pig IgG. The C2 domain may therefore provide an ideal material for the purification and detection of immunoglobulin G from various mammals..
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2013 |
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Erschienen: |
2013 |
Enthalten in: |
Zur Gesamtaufnahme - volume:35 |
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Enthalten in: |
Biotechnology letters - 35(2013), 9 vom: 21. Mai, Seite 1441-1447 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Cao, Yongsheng [VerfasserIn] |
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Links: |
Volltext [lizenzpflichtig] |
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BKL: | |
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Themen: |
Biological affinity |
Anmerkungen: |
© Springer Science+Business Media Dordrecht 2013 |
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doi: |
10.1007/s10529-013-1221-7 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
OLC211167303X |
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100 | 1 | |a Cao, Yongsheng |e verfasserin |4 aut | |
245 | 1 | 0 | |a Characterization of the optimized C2 domain of protein G: finding its additional chicken IgY-binding ability |
264 | 1 | |c 2013 | |
336 | |a Text |b txt |2 rdacontent | ||
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520 | |a Abstract The C2 domain of streptococcal protein G is a small (55 residue) peptide with immunoglobulin-binding activity. Following codon optimization, the gene was divided into four oligonucleotide fragments and amplified by overlap PCR. The recombinant plasmid pET30a-C2 was transformed into Escherichia coli Rosetta (DE3) PLysS for expression. After purification by Ni–NTA, the fusion protein was identified by western-blotting, Dot-ELISA and ELISA. His-tagged C2 bound to human, rabbit, cattle, pig, goat, mouse or guinea pig IgG had no affinity for goose, duck, wild duck, wild turkey and red-crowned crane IgY. Its affinity for chicken IgY, however, was comparable to that of guinea pig IgG. The C2 domain may therefore provide an ideal material for the purification and detection of immunoglobulin G from various mammals. | ||
650 | 4 | |a Biological affinity | |
650 | 4 | |a C2 domain of streptococcal protein G | |
650 | 4 | |a Chicken IgY-binding ability | |
650 | 4 | |a Expression and purification | |
650 | 4 | |a Gene optimization | |
700 | 1 | |a Li, Di |4 aut | |
700 | 1 | |a Cao, Chong |4 aut | |
700 | 1 | |a Gao, Mingchun |4 aut | |
700 | 1 | |a Zhang, Runxiang |4 aut | |
700 | 1 | |a Ma, Bo |4 aut | |
700 | 1 | |a Wang, Junwei |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Biotechnology letters |d Springer Netherlands, 1979 |g 35(2013), 9 vom: 21. Mai, Seite 1441-1447 |h Online-Ressource |w (DE-627)312808356 |w (DE-600)2012203-2 |w (DE-576)107586002 |x 1573-6776 |7 nnns |
773 | 1 | 8 | |g volume:35 |g year:2013 |g number:9 |g day:21 |g month:05 |g pages:1441-1447 |
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