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作为用于蛋白质识别的合成抗体的分子印迹聚合物:下一代技术。

Molecularly Imprinted Polymers as Synthetic Antibodies for Protein Recognition: The Next Generation.

作者信息

Tse Sum Bui Bernadette, Mier Alejandra, Haupt Karsten

机构信息

Université de Technologie de Compiègne, CNRS Laboratory for Enzyme and Cell Engineering, Rue du Docteur Schweitzer, CS 60319, Compiègne, 60203 Cedex, France.

出版信息

Small. 2023 Mar;19(13):e2206453. doi: 10.1002/smll.202206453. Epub 2023 Jan 17.

DOI:10.1002/smll.202206453
PMID:36650929
Abstract

Molecularly imprinted polymers (MIPs) are chemical antibody mimics obtained by nanomoulding the 3D shape and chemical functionalities of a desired target in a synthetic polymer. Consequently, they possess exquisite molecular recognition cavities for binding the target molecule, often with specificity and affinity similar to those of antigen-antibody interactions. Research on MIPs targeting proteins began in the mid-90s, and this review will evaluate the progress made till now, starting from their synthesis in a monolith bulk format through surface imprinting to biocompatible soluble nanogels prepared by solid-phase synthesis. MIPs in the latter format will be discussed more in detail because of their tremendous potential of replacing antibodies in the biomedical domain like in diagnostics and therapeutics, where the workforce of antibodies is concentrated. Emphasis is also put on the development of epitope imprinting, which consists of imprinting a short surface-exposed fragment of a protein, resulting in MIPs capable of selectively recognizing the whole macromolecule, amidst others in complex biological media, on cells or tissues. Thus selecting the 'best' peptide antigen is crucial and in this context a rational approach, inspired from that used to predict peptide immunogens for peptide antibodies, is described for its unambiguous identification.

摘要

分子印迹聚合物(MIP)是通过在合成聚合物中对所需靶标的三维形状和化学功能进行纳米成型而获得的化学抗体模拟物。因此,它们具有用于结合靶分子的精确分子识别腔,其特异性和亲和力通常与抗原 - 抗体相互作用相似。针对蛋白质的MIP研究始于90年代中期,本综述将评估迄今为止所取得的进展,从整体块状形式的合成开始,经过表面印迹,到通过固相合成制备的生物相容性可溶性纳米凝胶。由于后一种形式的MIP在生物医学领域(如诊断和治疗,抗体的应用集中于此)具有替代抗体的巨大潜力,因此将更详细地讨论。还强调了表位印迹的发展,表位印迹包括对蛋白质的短表面暴露片段进行印迹,从而产生能够在复杂生物介质、细胞或组织中选择性识别整个大分子的MIP。因此,选择“最佳”肽抗原至关重要,在此背景下,描述了一种受预测肽抗体的肽免疫原的方法启发的合理方法,用于明确鉴定。

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