Paulo Joao A, Hawrot Edward
Graduate Program in Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, RI 02912, USA.
Anal Biochem. 2009 Jun 1;389(1):86-8. doi: 10.1016/j.ab.2009.03.011. Epub 2009 Mar 14.
alpha-Bungarotoxin (alpha-bgtx)-binding proteins, including certain nicotinic acetylcholine receptors and acetylcholine-binding proteins (AChBPs), are frequently characterized with radioisotope-labeled alpha-bgtx-binding assays. Such assays, however, preclude investigations of binding interactions in real time and are hampered by the inconveniences associated with radioisotope-labeled reagents. We used surface plasmon resonance-based technology (BIAcore) to investigate the binding of recombinant AChBP to CM-5 sensor chip surfaces with directly immobilized alpha-bgtx. We validated our BIAcore results by comparing the same biological samples using the traditional (125)I-labeled alpha-bgtx-binding assay. An alpha-bgtx sensor chip, as described here, enables detailed, real-time, radioisotope-free interaction studies that can greatly facilitate the characterization of novel alpha-bgtx-binding proteins and complexes.
α-银环蛇毒素(α-bgtx)结合蛋白,包括某些烟碱型乙酰胆碱受体和乙酰胆碱结合蛋白(AChBPs),常通过放射性同位素标记的α-bgtx结合试验来表征。然而,此类试验无法实时研究结合相互作用,且受到与放射性同位素标记试剂相关不便之处的阻碍。我们使用基于表面等离子体共振的技术(BIAcore)来研究重组AChBP与直接固定有α-bgtx的CM-5传感器芯片表面的结合。我们通过使用传统的(125)I标记的α-bgtx结合试验比较相同的生物样品,验证了我们的BIAcore结果。如本文所述的α-bgtx传感器芯片能够进行详细、实时、无放射性同位素的相互作用研究,这可极大地促进新型α-bgtx结合蛋白和复合物的表征。