Chen B, Bestetti G, Day R M, Turner A P
Cranfield Biotechnology Centre, Cranfield University, Bedfordshire, UK.
Biosens Bioelectron. 1998 Oct 1;13(7-8):779-85. doi: 10.1016/s0956-5663(98)00042-6.
This paper reports the synthesis and screening of a combinatorial peptide library for new affinity ligands for glycosylated haemoglobin (HbA1c), which is an important indicator of diabetes control. The new ligands are suitable for large-scale synthesis and overcome the disadvantages of antibodies (unstable and expensive to produce etc.), while remaining as efficient as antibodies in binding to the analyte. The library consisted of 262,144 hexapeptides synthesised using the one-bead-one-compound technique. The hexapeptides attached onto beads were screened with glycosylated haemoglobin HbA1c. The structures of the peptides exhibiting high affinity were characterised by Edman microsequencing. Computer modelling simulation of one of the lead sequences has shown that this class of ligand has a high affinity and specificity for glycosylated haemoglobin.
本文报道了用于筛选糖化血红蛋白(HbA1c)新型亲和配体的组合肽库的合成与筛选,HbA1c是糖尿病控制的重要指标。这些新型配体适合大规模合成,克服了抗体的缺点(如生产不稳定且昂贵等),同时在与分析物结合方面与抗体一样高效。该文库由使用单珠单化合物技术合成的262,144种六肽组成。将附着在珠子上的六肽用糖化血红蛋白HbA1c进行筛选。通过埃德曼微量测序对表现出高亲和力的肽的结构进行了表征。对其中一个先导序列的计算机建模模拟表明,这类配体对糖化血红蛋白具有高亲和力和特异性。