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基于肽类的 SP-C 类似物的螺旋侧链化学:平衡结构刚性和仿生特性。

Helical side chain chemistry of a peptoid-based SP-C analogue: Balancing structural rigidity and biomimicry.

机构信息

Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois.

Department of Bioengineering, Stanford University, Stanford, California.

出版信息

Biopolymers. 2019 Jun;110(6):e23277. doi: 10.1002/bip.23277. Epub 2019 Apr 10.

Abstract

Surfactant protein C (SP-C) is an important constituent of lung surfactant (LS) and, along with SP-B, is included in exogenous surfactant replacement therapies for treating respiratory distress syndrome (RDS). SP-C's biophysical activity depends upon the presence of a rigid C-terminal helix, of which the secondary structure is more crucial to functionality than precise side-chain chemistry. SP-C is highly sequence-conserved, suggesting that the β-branched, aliphatic side chains of the helix are also important. Nonnatural mimics of SP-C were created using a poly-N-substituted glycine, or "peptoid," backbone. The mimics included varying amounts of α-chiral, aliphatic side chains and α-chiral, aromatic side chains in the helical region, imparting either biomimicry or structural rigidity. Biophysical studies confirmed that the peptoids mimicked SP-C's secondary structure and replicated many of its surface-active characteristics. Surface activity was optimized by incorporating both structurally rigid and biomimetic side chain chemistries in the helical region indicating that both characteristics are important for activity. By balancing these features in one mimic, a novel analogue was created that emulates SP-C's in vitro surface activity while overcoming many of the challenges related to natural SP-C. Peptoid-based analogues hold great potential for use in a synthetic, biomimetic LS formulation for treating RDS.

摘要

表面活性蛋白 C(SP-C)是肺表面活性剂(LS)的重要组成部分,与 SP-B 一起包含在外源性表面活性剂替代疗法中,用于治疗呼吸窘迫综合征(RDS)。SP-C 的生物物理活性取决于刚性 C 端螺旋的存在,其中二级结构对功能比精确的侧链化学更关键。SP-C 高度序列保守,表明螺旋的β支链、脂肪侧链也很重要。使用聚-N-取代甘氨酸或“肽类”骨架创建了 SP-C 的非天然模拟物。这些模拟物在螺旋区域包含不同数量的α-手性、脂肪侧链和α-手性、芳香族侧链,赋予其生物模拟或结构刚性。生物物理研究证实,肽类模拟物模拟了 SP-C 的二级结构,并复制了其许多表面活性特性。通过在螺旋区域中结合结构刚性和生物模拟侧链化学,表面活性得到了优化,表明这两种特性对活性都很重要。通过在一种模拟物中平衡这些特征,创建了一种新型类似物,该类似物模拟了 SP-C 的体外表面活性,同时克服了与天然 SP-C 相关的许多挑战。基于肽类的类似物在用于治疗 RDS 的合成、仿生 LS 配方中具有很大的应用潜力。

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