Department of Pharmaceutical Sciences, North Dakota State University, Fargo, North Dakota, USA.
Nat Protoc. 2010 Jan;5(1):39-50. doi: 10.1038/nprot.2009.195. Epub 2009 Dec 17.
Collagen-mimetic peptides and lipopeptides are widely used as substrates for matrix degrading enzymes, as new biomaterials for tissue engineering, as drug delivery systems and so on. However, the preparation and subsequent purification of these peptides and their fatty-acid conjugates are really challenging. Herein, we report a rapid microwave-assisted, solid-phase synthetic protocol to prepare the fatty-acid conjugated, triple-helical peptides containing the cleavage site for the enzyme matrix metalloproteinase-9 (MMP-9). We employed a PEG-based resin as the solid support and the amino acids were protected with Fmoc- and tert-butyl groups. The amino acids were coupled at 50 degrees C (25 W of microwave power) for 5 min. The deprotection reactions were carried out at 75 degrees C (35 W of microwave power) for 3 min. Using this protocol, a peptide containing 23 amino acids was synthesized and then conjugated to stearic acid in 14 h.
胶原模拟肽和脂肽被广泛用作基质降解酶的底物,也被用作组织工程的新型生物材料、药物传递系统等。然而,这些肽及其脂肪酸缀合物的制备和随后的纯化确实具有挑战性。在此,我们报告了一种快速的微波辅助固相合成方案,用于制备包含酶基质金属蛋白酶-9 (MMP-9) 切割位点的脂肪酸共轭三螺旋肽。我们采用基于 PEG 的树脂作为固体载体,氨基酸用 Fmoc-和叔丁基保护。氨基酸在 50°C(微波功率 25 W)下偶联 5 分钟。脱保护反应在 75°C(微波功率 35 W)下进行 3 分钟。使用该方案,合成了含有 23 个氨基酸的肽,然后在 14 小时内与硬脂酸缀合。