Savinov G V, Shepelyakovskaya A O, Boziev Kh M, Brovko F A, Laman A G
Pushchino Branch of Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Pushchino, Moscow Region, 142290, Russia.
Biochemistry (Mosc). 2014 Feb;79(2):131-8. doi: 10.1134/S0006297914020060.
The method for searching for ligands exerting an adjuvant effect is described. The method involves isolation of polysomes using an immobilized peptide mimetic of N-acetylglucosaminyl-N-acetylmuramyl dipeptide (GMDP) - RN-peptide. After the affinity chromatography and washing, RN-peptide complexes with the target sequences were dissociated with guanidine hydrochloride. The obtained mRNA was used for cDNA synthesis and subsequent cloning in an expression vector. Further studies showed the effectiveness of this method. Clones interacting with the peptide were selected using biotinylated RN-peptide. It was found that all clones encode a sequence identical to the protein YB-1. Recombinant antibodies against protein YB-1 were selected from a phage display human scFv library. Using these antibodies, we determined the binding constant of RN-peptide to protein YB-1. Competitive analysis showed that RN-peptide and GMDP compete for the same portion of YB-1 at molar ratio 1 : 12.
描述了寻找具有佐剂效应的配体的方法。该方法包括使用N-乙酰葡糖胺基-N-乙酰胞壁酰二肽(GMDP)-RN-肽的固定化肽模拟物分离多核糖体。经过亲和层析和洗涤后,用盐酸胍解离与靶序列的RN-肽复合物。所得mRNA用于cDNA合成并随后克隆到表达载体中。进一步的研究表明了该方法的有效性。使用生物素化的RN-肽选择与该肽相互作用的克隆。发现所有克隆编码的序列与蛋白质YB-1相同。从噬菌体展示人单链抗体库中选择针对蛋白质YB-1的重组抗体。使用这些抗体,我们测定了RN-肽与蛋白质YB-1的结合常数。竞争分析表明,RN-肽和GMDP以1:12的摩尔比竞争YB-1的同一部分。