Chemical Modification and Denaturation Effects on the Hemagglutinating Activity of Two Pterocarpus Species Seeds Lectins

Morenikeji Tolulope Folowosele, O. Odekanyin, Adenike Oluwaseun Adefila, Sinaola Praise Oyepitan, Eniola Racheal Owolabi, Ayomide Ifeoluwa Alobaloye
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Abstract

Aims: Pterocarpus osun and Pterocarpus soyauxii seeds lectins were subjected to various chemical modifications in order to detect the amino acid residues involved in their hemagglutinating and sugar-binding activities. Methodology: The lectins were purified using salt precipitation and size exclusion chromatography. Hemagglutinating activity and sugar specificity of the lectins were also established. Chemical modification of arginine was done using phenylglyoxal hydrate, and 5,5- dithiobis-(2-nitrobenzoic acid) (DTNB) was used to modify cysteine. Phenylmethylsulfonyl fluoride (PMSF) was employed for serine modification and tryptophan residue was modified with N-bromosuccinimide (NBS). Denaturants effects on the hemagglutinating activity were carried out with chaotropic agents, acid, disulphide bridge reducer and cross-linker agent. Results: Pterocarpus osun seeds lectin is mannose specific while Pterocarpus soyauxii seeds lectin is galactose/lactose-binding lectin. Hemagglutinating activities of the two lectins were completely lost when tryptophan residue was modified with NBS and the loss was reversed by dialysis. Modifications of Cysteine, Arginine and Serine have no effect on the hemagglutinating activity of P. osun lectin. Nevertheless, the modifications of same amino acids slightly reduced the activity of P. soyauxii lectin, which dialysis and prolonged incubation were able to overturn. Mannose was found to bind and inhibit hemagglutinating activity of P. osun lectin in the presence of various modifiers but galactose and lactose could not inhibit the hemagglutinating activity of P. soyauxii lectin in the presence of modifiers. All denaturants employed significantly affected the hemagglutinating activity of the two lectins. However, the effects were reversible except for P. osun lectin denatured with 8M urea. Conclusion: The results revealed that tryptophan residue is essential for hemagglutinating activity of the Pterocarpus species seeds lectins studied in this research. Cysteine, Arginine and Serine are also needed for sugar binding by P. soyauxii lectin but not so important in P. osun sugar binding ability.
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化学修饰和变性对两种紫檀种子凝集素血凝活性的影响
目的:对紫檀和大叶紫檀种子凝集素进行各种化学修饰,以检测参与其血凝和糖结合活性的氨基酸残基:用盐沉淀法和尺寸排阻色谱法纯化凝集素。还确定了凝集素的血凝活性和糖特异性。使用苯乙二醛水合物对精氨酸进行化学修饰,使用 5,5-二硫双(2-硝基苯甲酸)(DTNB)对半胱氨酸进行修饰。苯甲基磺酰氟(PMSF)用于修饰丝氨酸,N-溴琥珀酰亚胺(NBS)修饰色氨酸残基。变性剂对血凝活性的影响是通过混沌剂、酸、二硫桥还原剂和交联剂来实现的:结果:黄檀种子凝集素是甘露糖特异性凝集素,而黄檀种子凝集素是半乳糖/乳糖结合凝集素。用 NBS 修饰色氨酸残基后,这两种凝集素的血凝活性完全丧失,透析可逆转这种丧失。半胱氨酸、精氨酸和丝氨酸的修饰对 P. osun 凝集素的血凝活性没有影响。然而,对相同氨基酸的修饰会略微降低大豆凝集素的活性,透析和延长孵育时间可将其逆转。研究发现,在各种变性剂存在的情况下,甘露糖能结合并抑制大豆异黄酮凝集素的血凝活性,但在变性剂存在的情况下,半乳糖和乳糖不能抑制大豆异黄酮凝集素的血凝活性。所有使用的变性剂都会明显影响两种凝集素的血凝活性。然而,除了用 8M 尿素变性的 P. osun 凝集素外,其他影响都是可逆的:结果表明,色氨酸残基对本研究中研究的紫檀种子凝集素的血凝活性至关重要。半胱氨酸、精氨酸和丝氨酸也是大豆异黄酮凝集素糖结合所必需的,但对大枣异黄酮凝集素糖结合能力的影响不大。
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