Shi Xiaodong, Liu Yinghuan, Zhao Rongtong, Li Zigang
Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School.
Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School;
J Vis Exp. 2018 Aug 1(138):57356. doi: 10.3791/57356.
Here, we describe a detailed protocol for the preparation of thioether-tethered peptides using on-resin intramolecular/intermolecular thiol-ene hydrothiolation. In addition, this protocol describes the preparation of vinyl-sulfide-tethered peptides using in-solution intramolecular thiol-yne hydrothiolation between amino acids that possess alkene/alkyne side chains and cysteine residues at i, i+4 positions. Linear peptides were synthesized using a standard Fmoc-based solid-phase peptide synthesis (SPPS). Thiol-ene hydrothiolation is carried out using either an intramolecular thio-ene reaction or an intermolecular thio-ene reaction, depending on the peptide length. In this research, an intramolecular thio-ene reaction is carried out in the case of shorter peptides using on-resin deprotection of the trityl groups of cysteine residues following the complete synthesis of the linear peptide. The resin is then set to UV irradiation using photoinitiator 4-methoxyacetophenone (MAP) and 2-hydroxy-1-[4-(2-hydroxyethoxy)-phenyl]-2-methyl-1-propanone (MMP). The intermolecular thiol-ene reaction is carried out by dissolving Fmoc-Cys-OH in an N,N-dimethylformamide (DMF) solvent. This is then reacted with the peptide using the alkene-bearing residue on resin. After that, the macrolactamization is carried out using benzotriazole-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate (PyBop), 1-hydroxybenzotriazole (HoBt), and 4-Methylmorpholine (NMM) as activation reagents on the resin. Following the macrolactamization, the peptide synthesis is continued using standard SPPS. In the case of the thio-yne hydrothiolation, the linear peptide is cleaved from the resin, dried, and subsequently dissolved in degassed DMF. This is then irradiated using UV light with photoinitiator 2,2-dimethoxy-2-phenylacetophenone (DMPA). Following the reaction, DMF is evaporated and the crude residue is precipitated and purified using high-performance liquid chromatography (HPLC). These methods could function to simplify the generation of thioether-tethered cyclic peptides due to the use of the thio-ene/yne click chemistry that possesses superior functional group tolerance and good yield. The introduction of thioether bonds into peptides takes advantage of the nucleophilic nature of cysteine residues and is redox-inert relative to disulfide bonds.
在此,我们描述了一种使用树脂上分子内/分子间硫醇-烯氢硫醇化制备硫醚连接肽的详细方案。此外,该方案还描述了使用具有烯烃/炔烃侧链的氨基酸与i、i + 4位的半胱氨酸残基之间的溶液内分子内硫醇-炔氢硫醇化制备乙烯基硫醚连接肽的方法。线性肽使用基于Fmoc的标准固相肽合成(SPPS)进行合成。硫醇-烯氢硫醇化根据肽的长度使用分子内硫-烯反应或分子间硫-烯反应进行。在本研究中,对于较短的肽,在完成线性肽的合成后,使用树脂上半胱氨酸残基三苯甲基的脱保护进行分子内硫-烯反应。然后使用光引发剂4-甲氧基苯乙酮(MAP)和2-羟基-1-[4-(2-羟基乙氧基)-苯基]-2-甲基-1-丙酮(MMP)对树脂进行紫外线照射。分子间硫醇-烯反应通过将Fmoc-Cys-OH溶解在N,N-二甲基甲酰胺(DMF)溶剂中进行。然后使其与树脂上带有烯烃的残基的肽反应。之后,使用苯并三唑-1-基-氧基三吡咯烷基鏻六氟磷酸盐(PyBop)、1-羟基苯并三唑(HoBt)和4-甲基吗啉(NMM)作为活化试剂在树脂上进行大环化反应。大环化反应后,使用标准SPPS继续进行肽合成。在硫-炔氢硫醇化的情况下,将线性肽从树脂上切割下来,干燥,随后溶解在脱气的DMF中。然后使用光引发剂2,2-二甲氧基-2-苯基苯乙酮(DMPA)进行紫外线照射。反应后,蒸发DMF,将粗产物沉淀并使用高效液相色谱(HPLC)进行纯化。由于使用了具有优异官能团耐受性和良好产率的硫-烯/炔点击化学,这些方法可以简化硫醚连接环肽的生成。将硫醚键引入肽中利用了半胱氨酸残基的亲核性质,并且相对于二硫键是氧化还原惰性的。