Tob/BTG家族蛋白框A区衍生的5-mer合成肽对淀粉样蛋白片段肽的催化活性比较

Rina Nakamura, M. Konishi, Y. Higashi, M. Saito, T. Akizawa
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引用次数: 6

摘要

我们之前报道了来自Tob/BTG蛋白家族Box A区域的9聚肽JAL-TA9 (YKGSGFRMI)的催化活性。这是第一次报道短合成肽的催化活性。因此,我们使用“Catalytide”(催化肽)作为具有水解酶活性的肽的总称。对JAL-TA9的核磁共振研究表明,催化活性所需的最小序列是一个5聚肽(GSGFR)。在本研究中,我们检测了该5聚肽对Aβ片段肽Aβ1-20和Aβ11-29的催化活性,以寻找下一个催化肽。所有被鉴定为催化剂的肽的活性,特别是GQAYR (BTG3)和GQAFR (BTG4)的活性都高于GSGFR (to1和2)和GSGYR (BTG1和2)。这些催化剂的裂解机制尚不清楚,需要进一步研究。尽管如此,作为治疗阿尔茨海默病(AD)的新策略,5-mer Catalytides是开发肽药物的有吸引力的候选者。APP:淀粉样前体蛋白;Aβ:淀粉样蛋白β;AD:阿尔茨海默病;人血清白蛋白;TFA:三氟乙酸;HPLC:高效液相色谱法;核磁共振:核磁共振。
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Comparison of the catalytic activities of 5-mer synthetic peptides derived from Box A region of Tob/BTG family proteins against the amyloid-beta fragment peptides
We previously reported the catalytic activity of 9-mer peptide, JAL-TA9 (YKGSGFRMI), derived from the Box A region of Tob/BTG family of proteins. This was the first report of the catalytic activity of shorter synthetic peptides. Therefore, we used ‘Catalytide’ (catalytic peptide) as the general term for peptides possessing the hydrolase activity. NMR study of JAL-TA9 suggested that the minimum sequence required for the catalytic activity is a 5-mer peptide (GSGFR). In this study, we examined the catalytic activity of this 5-mer peptide against Aβ fragment peptides, Aβ1-20 and Aβ11-29, to find the next Catalytide. Activity of all peptides identified as Catalytides, especially, GQAYR (BTG3) and GQAFR (BTG4), was higher activity than that of GSGFR (Tob1 and 2) and GSGYR (BTG1 and 2). The cleavage mechanism of these Catalytides is still not well understood and needs further investigation. Nonetheless, 5-mer Catalytides are attractive candidates for the development of peptide drugs as a new strategy for treating Alzheimer’s disease (AD). Abbreviations: APP: Amyloid Precursor Protein; Aβ: Amyloid Beta; AD: Alzheimer’s Disease; HSA: Human Serum Albumin; TFA: Trifluoroacetic Acid; HPLC: High-Performance Liquid Chromatography; NMR: Nuclear Magnetic Resonance.
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