Tikhonov Sergei L, Babich Olga O, Sukhikh Stanislav A, Tikhonova Natalia V, Chernukha Irina M
Department of Food Engineering of Agricultural Production, Ural State Agrarian University, Ekaterinburg, Russia.
Department of Chemical Technology of Wood, Biotechnology and Nanomaterials, Ural State Forest Engineering University, Ekaterinburg, Russia.
Curr Protein Pept Sci. 2025 Jun 16. doi: 10.2174/0113892037356348250523031542.
Thrombosis is a major cause of mortality from cardiovascular disease (CVD). The use of known antithrombin drugs is limited by the presence of side effects and complications. Peptides may be promising antithrombin agents.
A peptide having the amino acid sequence QLSNGLFLFVDYLWW, designated as QW-13, was designed, synthesized, and used as a research object to evaluate the efficiency of the algorithm.
The solid-phase Fmoc (SPPS) method, followed by purification by high-performance liquid chromatography (HPLC) was used for synthesis. The molecular weight distribution of the peptide was estimated by mass spectrometry. Peptide identification was performed using the MALDI-TOF MS Ultraflex method. Mass spectra were analyzed using the Mascot program. To confirm the efficiency of the algorithm, the antithrombin effect of the peptide was studied, which was evaluated by the activated partial thromboplastin time (APTT) of human citrate blood plasma coagulation.
A decision tree algorithm was developed to predict antithrombin activity and bioavailability of oral peptides. The top-down inductions of decision tree algorithms were used to create the algorithm. The decision tree is pruned if there is a mismatch in the peptide under study. Algorithm criteria or descriptors include amino acid sequence, number of amino acids, molecular weight, clinical potency, body distribution and metabolism index, plasma clearance, and half-life. According to the algorithm, if the result of "Antithrombin Peptide" is positive, it is concluded that it is bioavailable and effective for clinical use. To validate and evaluate the efficiency of the algorithm, a peptide containing antithrombin amino acid sequences was synthesized. The algorithm found the peptide to be antithrombin and bioavailable. The results of the biological activity of the peptide were confirmed in an in vitro experiment.
Employing a decision tree method to assess the antithrombin activity and bioavailability of peptides can facilitate the development of effective oral peptides, hence minimizing the development time and the quantity of in vitro and in vivo studies required to validate efficacy.
血栓形成是心血管疾病(CVD)致死的主要原因。已知抗凝血酶药物的使用受到副作用和并发症的限制。肽类可能是有前景的抗凝血酶药物。
设计、合成了一种氨基酸序列为QLSNGLFLFVDYLWW的肽,命名为QW-13,并将其作为研究对象来评估该算法的效率。
采用固相Fmoc(SPPS)法合成,随后通过高效液相色谱(HPLC)进行纯化。通过质谱估计肽的分子量分布。使用MALDI-TOF MS Ultraflex方法进行肽鉴定。使用Mascot程序分析质谱。为了确认该算法的效率,研究了该肽的抗凝血酶作用,通过人枸橼酸盐血浆凝血的活化部分凝血活酶时间(APTT)进行评估。
开发了一种决策树算法来预测口服肽的抗凝血酶活性和生物利用度。使用决策树算法的自顶向下归纳法来创建该算法。如果所研究的肽存在不匹配情况,则对决策树进行修剪。算法标准或描述符包括氨基酸序列、氨基酸数量、分子量、临床效力、体内分布和代谢指数、血浆清除率和半衰期。根据该算法,如果“抗凝血酶肽”的结果为阳性,则得出该肽具有生物利用度且对临床使用有效的结论。为了验证和评估该算法的效率,合成了一种含有抗凝血酶氨基酸序列的肽。该算法发现该肽具有抗凝血酶活性且具有生物利用度。该肽的生物活性结果在体外实验中得到了证实。
采用决策树方法评估肽的抗凝血酶活性和生物利用度有助于开发有效的口服肽,从而最大限度地减少验证疗效所需的体外和体内研究的开发时间和数量。