Tillib S V, Panasyuk M V, Goryaynova O S, Ivanova T I
Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Dokl Biochem Biophys. 2025 Apr;521(1):192-197. doi: 10.1134/S1607672924601525. Epub 2025 Apr 11.
Immunoassay (IA) methods performed in the wells of a polystyrene microplate are the basis of diagnostic studies. In the "sandwich" IA, a fundamentally important initial stage is the immobilization of anchor antibodies in the well of the plate, designed for specific binding of a given antigen from a biological fluid. One of the very promising options for antigen-recognizing molecules are single-domain antibodies (nanoantibodies, Nbs). The use of Nbs as anchor antibodies is hampered by their low efficiency of functioning after passive adsorption in the well of the plate. The development of a new format and immobilization method in the case of Nbs are fundamentally important for overcoming this problem. This work describes the development of a new format of an anchor bispecific nanoantibody (anchor-Nb) to improve the efficiency of both passive adsorption of anchor-Nb and subsequent stages of immobilization and detection of the target antigen in the well of a polystyrene plate.
在聚苯乙烯微孔板孔中进行的免疫测定(IA)方法是诊断研究的基础。在“夹心”免疫测定中,一个至关重要的初始阶段是将锚定抗体固定在微孔板的孔中,该抗体用于特异性结合生物流体中的特定抗原。单域抗体(纳米抗体,Nbs)是抗原识别分子中非常有前景的选择之一。纳米抗体作为锚定抗体使用时,由于其在微孔板孔中被动吸附后的功能效率较低而受到阻碍。开发纳米抗体的新形式和固定方法对于解决这一问题至关重要。这项工作描述了一种新型锚定双特异性纳米抗体(锚定-Nb)的开发,以提高锚定-Nb的被动吸附效率以及随后在聚苯乙烯板孔中固定和检测目标抗原的效率。