Publication | Open Access
Expression, purification, and characterization of a diabody against the most important angiogenesis cell receptor: Vascular endothelial growth factor receptor 2
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Citations
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References
2012
Year
Purification Vegfr2-specific DiabodyImmunologyPathologyImmunotherapyCellular PhysiologyTumor BiologyAngiogenesisFibroblast Growth FactorAntibody EngineeringCell SignalingVariable FragmentsDerivative FragmentsVascular BiologyNeovascularizationVascular Endothelial Growth FactorAntibody ScreeningCell BiologyTumor MicroenvironmentSignal TransductionEndothelial DysfunctionMedicineExtracellular Matrix
Antibodies and their derivative fragments have long been used as tools in a variety of applications, in fundamental research work, biotechnology, diagnosis, and therapy. Camels produce single heavy-chain antibodies (VHH) in addition to usual antibodies. These minimal-sized binders are very robust and bind the antigen with high affinity in a monomeric state. Vascular endothelial growth factor recepror-2 (VEGFR2) is an important tumor-associated receptor that blockade of its signaling can lead to the inhibition of neovascularization and tumor metastasis. Here, we describe the construction, expression, and purification VEGFR2-specific Diabody. Two variable fragments of a same camel anti-VEGFR2 antibody were linked together by the upper hinge segment of antibody to make a diabody. We showed the ability of diabody to recognition of VEGFR2 on the cell surface by FACS. Diabodies can be produced in the low-cost prokaryotic expression system, so they are suitable molecules for diagnostic and therapeutic issues.
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