pSEX81 plasmid vector丝状噬菌体表面展示载体抗体表面展示载体 BioVector NTCC质粒载体菌种细胞基因保藏中心

pSEX81 plasmid vector丝状噬菌体表面展示载体抗体表面展示载体

pSEX81丝状噬菌体表面展示载体抗体表面展示载体，可方便地插入抗体重链和轻链可变区编码序列，在M13丝状噬菌体表面展示功能性单链Fv抗体与pIII融合蛋白。
pSEX81 was used for the convenient insertion of heavy and light chain variable domain coding regions and for production of functional single-chain Fv antibody-pIII fusion proteins on the surface of M13 bacteriophages. The corresponding DNA fragments of human or mouse origin can be amplified by PCR.The amplified gene fragments encoding the variable heavy or light chain domain are cloned in-frame between a signal peptide sequence of bacterial pectate lyase (pelB) for the secretion of the fusion protein into the periplasmic space, and the pIII gene of M13 bacteriophage. The VH and VL genes were joined by a DNA-fragment coding for a flexible 18 amino acid residue linker containing the first six amino acids of the CH1 constant region domain and the hydrophilic pig brain alpha-tubulin peptide sequence EEGEFSEAR. The vector backbone further provides a strong promotor, the T7 terminator, the ColE1 origin of replication, the intergenic region of phage F1 and an ampicillin resistance marker for selection.

Quantity 5 µg
Host E. coli lacIq genotype (e.g. XL1-Blue)
Purification Plasmid Purification Kit
Intended use Research use only
Concentration 0.5 µg/µl in TE buffer
Purity OD 260/280 ratio: 1.8-2.0
Quality check Efficiency in standard transformation procedure with chemically competent E. coli cells (XL1-Blue) > 1E+08 cfu/µg DNA
Stability Minimum 1 year when stored at -20°C
Vector 4883 bp, AmpR
Cloning sites MluI and NotI for light chain VL genes, NcoI and HindIII for heavy chain VH genes
Introduction
Within the past decade, recombinant antibody technologies have been widely used to produce various single-chain Fv antibody fragments of different specificity. The randomized combination of PCR-amplified immunoglobulin variable heavy and light chain genes further led to the construction of large human or mouse scFv antibody libraries. The isolation of high affinity antibodies derived thereof was established by the expression of recombinant antibody fragments on the surface protein pIII of M13 bacteriophages, which can be rapidly screened against antigens bound to a solid phase.
The M13 bacteriophage protein pIII is located at one end of its tubular virion structure. It is a relative flexible and accessible molecule composed of two functional domains: an N-terminal domain that binds to the F pilus of bacteria during infection and a C-terminal domain buried within the virion. ScFv antibody fragments can be inserted near its N-terminus without destroying its function.
BioVector now offers the phagemid cassette vector pSEX81 for the expression of functional single-chain Fv antibody - pIII fusion proteins on the surface of M13 bacteriophages. The phagemid was specifically constructed for cloning of immunoglobulin heavy and light chain gene fragments isolated from human or mouse antibody libraries generated with BioVector's PCR primer sets F2000 or F2010.
Vector Design
The cassette vector pSEX81 was designed for the convenient insertion of heavy and light chain variable domain coding regions and for production of functional single-chain Fv antibody - pIII fusion proteins on the surface of M13 bacteriophages. The corresponding DNA fragments of human or mouse origin can be amplified by PCR using BioVector's primer sets F2000 or F2010, respectively. The amplified gene fragments encoding the variable heavy or light chain domain are cloned in-frame between a signal peptide sequence of bacterial pectate lyase (pelB) for the secretion of the fusion protein into the periplasmic space, and the pIII gene of M13 bacteriophage. The VH and VL genes were joined by a DNA-fragment coding for a flexible 18 amino acid residue linker containing the first six amino acids of the CH1 constant region domain and the hydrophilic pig brain alpha-tubulin peptide sequence EEGEFSEAR. The vector backbone further provides a strong promotor, the T7 terminator, the ColE1 origin of replication, the intergenic region of phage F1 and an ampicillin resistance marker for selection.
In pSEX81 the recognition sites of the restriction endonucleases Nco I and Hind III allow the insertion of a VH gene fragment. For insertion of a VL gene fragment the sites of the restriction endonucleases Mlu I and Not I are recommended.
Material Required
Equipment for DNA cloning
Preparation of Reagents
The DNA should be diluted and transfered into E. coli cells as described in standard protocols. Use an overnight culture of a single clone to extract enough DNA for the following cloning procedures.
Cloning procedure
The immunoglobulin heavy and light chain Fv domain coding regions must be cloned in-frame into pSEX81 (see attached graphic). To clone VH gene fragments the recognition sites of the restriction endonucleases Nco I and Hind III are recommended. VL gene fragments should be introduced by using the recognition sites of the enzymes Mlu I and Not I. The cloning sites of the selected Fv gene fragments have to match the corresponding amino acid positions given by the vector. Gene fragments derived from human or mouse origin with BioVector's PCR primer sets F2000 or F2010 can be directly cloned into pSEX81.
After cloning, the vector is ready-to-use for the expression of functional recombinant single-chain Fv antibody - pIII fusion proteins in E. coli. If the modified pSEX81 is co-transfected with M13 bacteriophage as described in standard protocols (Schmiedl et al., 2000; Schmiedl and Duebel, 2001), the scFv antibody - pIII fusion protein is expressed on the surface of resulting phage particles. For expression of scFv antibody libraries on the surface of M13 bacteriophages, we recommend to use the M13 Hyperphage from BioVector

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