生物信息学
体外
生物化学
大肠杆菌
重组DNA
结构相似性
生物
对接(动物)
肽序列
同源建模
分子模型
计算生物学
化学
分子动力学
结合位点
蛋白质二级结构
蛋白质结构
氨基酸
序列(生物学)
凝集素
分子生物学
序列同源性
血浆蛋白结合
序列比对
序列分析
肽
酶
作者
Guilherme Feijó de Sousa,Chrystian Nunes Gonçalves,Danillo de Oliveira Della Senta,Camila Garcia De Souza,Alice Calderipe de Lima,João Carlos Rodrigues,Maureen Legendre,David M. Markovitz,Luciano da Silva Pinto
标识
DOI:10.1007/s10930-026-10326-8
摘要
In this study, we conducted structural and comparative analyses of two recombinant banana lectins, rBanLec-like and H84T-BanLec, using both in silico and in vitro approaches. Sequence alignment showed 91.5% identity between the lectins, with differences in 12 amino acids. Structural modeling and secondary structure analysis indicated a high degree of structural similarity, with a root mean square deviation (RMSD) of 0.382 Å, suggesting that the sequence modifications did not lead to significant structural changes. Molecular docking experiments demonstrated a strong affinity of both lectins for mannose, with rBanLec-like exhibiting a lower binding free energy (− 6.6 kcal/mol) compared to H84T-BanLec (− 4.5 kcal/mol). Molecular dynamics simulations confirmed the stability of both proteins, although rBanLec-like displayed greater conformational flexibility. Expression in Escherichia coli showed successful production of both lectins, but rBanLec-like was detected in both soluble and insoluble fractions, whereas H84T-BanLec was exclusively obtained in the soluble fraction. Both lectins significantly inhibited the growth of colorectal adenocarcinoma cells by 62.6% and 76%, respectively. These findings contribute to the structural and functional understanding of banana lectins, highlighting their potential for biotechnological and therapeutic applications.
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