期刊论文详细信息
FEBS Letters
Use of GPI‐anchored proteins to study biomolecular interactions by surface plasmon resonance
Harrison, Patrick T1  Allen, Janet M1  Campbell, Ian W1 
[1] Division of Biochemistry and Molecular Biology and Department of Medicine and Therapeutics, The University of Glasgow, Glasgow G12 8QQ, UK
关键词: Surface plasmon resonance;    High affinity IgG receptor;    Glycosyl phosphatidyl inositol protein;    SPR;    surface plasmon resonance;    mAb;    monoclonal antibody;    FcγRI;    high affinity IgG receptor;    PI-PLC;    phosphatidyl inositol phospholipase C;    GPI;    glycosyl phosphatidyl inositol;   
DOI  :  10.1016/S0014-5793(98)00027-1
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

Surface plasmon resonance is a powerful tool to examine the kinetics of cell surface receptor-ligand interactions and requires only small amounts of protein. For these studies, one component is required in highly purified form to be coupled to the biosensor surface. The second component does not need to be purified. The human high affinity receptor for immunoglobulin G, FcγRI, presents a problem as the receptor itself cannot readily be produced in large amounts for purification and, as there are eight potential ligands for the receptor (human IgG1–4 and mouse IgG1, 2a, 2b and 3), it is difficult to immobilise the ligand. Using a previously established method for generating GPI-anchored proteins, we have produced and captured a soluble version of FcγRI and shown that it retains its affinity for human IgG1 and specificity for the different IgG subclasses. In addition, we also produced and captured a GPI-anchored version of the cell adhesion molecule CD2. This system circumvents the need for extensive receptor purification and is very rapid as solubilised receptors can be transferred from the cell surface to the sensor chip in 2 h. This system may be generally applicable for biosensor studies to other type I membrane proteins, and/or naturally occurring GPI-anchored proteins, especially where the interaction between a ligand and a panel of variant receptors is to be studied.

【 授权许可】

Unknown   

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