Development of a Biomimetic Lung Surfactant Replacement

仿生肺表面活性剂替代品的开发

• 批准号: 7790606
• 负责人: Annelise Emily Barron
• 金额: $ 32.86万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2001
• 资助国家: 美国
• 起止时间: 2001-09-01 至 2011-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7790606
• 关键词: Adsorption; Alkylation; Alveolar; Amino Acids; Animal Model; Animals; Behavior; Biocompatible; Biomimetics; Birth; Breathing; Carbon; Cattle; Cell Culture Techniques; Chemical Structure; Chemical Surfactants; Chemistry; Chimera organism; Complex Mixtures; Cystic Fibrosis; Development; Dimerization; Disease; Drug Formulations; Epithelial Cells; Equilibrium; Film; Fluorescence; Fluorescence Microscopy; Functional disorder; Funding; Glycine; Goals; Human; Image; Immune response; In Vitro; Incidence; Investigation; Length; Light; Lipid Bilayers; Lipids; Lung; Lung diseases; Maps; Medical; Microscopic; Modeling; Molecular; N-substituted Glycines; Newborn Respiratory Distress Syndrome; Oryctolagus cuniculus; Patients; Pattern; Peptide Hydrolases; Peptides; Peptoids; Phase; Play; Pneumonia; Poly A; Pregnancy; Premature Infant; Protein C; Proteins; Pulmonary Surfactant-Associated Protein B; Pulmonary Surfactant-Associated Proteins; Pulmonary Surfactants; Rattus; Replacement Therapy; Research Personnel; Resistance; Respiration; Respiratory physiology; Risk; Roentgen Rays; Role; Side; Solid; Structure; Structure-Activity Relationship; Surface; Surface Tension; Testing; Therapeutic; Toxic effect; Variant; Vertebral column; Vesicle; Viral; Work; Work of Breathing; X ray diffraction analysis; X-Ray Diffraction; analog; base; biomaterial compatibility; cost; design; fetal; functional mimics; improved; in vivo; innovation; molecular dynamics; monolayer; mouse model; next generation; novel; palmitoylation; pathogen; peptidomimetics; programs; protein B; research study; respiratory distress syndrome; surfactant; tool; transmission process

DESCRIPTION (provided by applicant): Several respiratory diseases and disorders could be better and more widely treated with an effective and low-cost biomimetic lung surfactant (LS) replacement. In present medical practice, LS replacements (used predominantly to treat neonatal respiratory distress syndrome) derive from animal lungs, are expensive, and carry risks of viral transmission and immune response. We propose to continue the development of a novel class of functional mimics of the lung surfactant proteins based on poly-N-substituted glycines (peptoids), which are sequence-specific heteropolymers synthesized on solid phase, similarly to peptides. Peptoids are protease resistant, and with proper sequence design can form stable, helical secondary structures that resist non-specific aggregation. Over the past 3.5 years, we have created and studied two different, novel classes of helical, amphipathic peptoid oligomers with sequence and structural similarity to (1) SP-B (residues 1-25) and (2) SP-C (residues 5-32). In vitro biophysical studies of the surface activities of these peptoid-based SP mimics in an LS-like lipid film demonstrate that the best designs within each class of mimics perform similarly to the natural peptides they are designed to replace. While initial results are very promising, much work remains to be done to develop peptoid-based SP mimics for a clinically useful, biomimetic LS replacement. We must now gain a deeper understanding of structure-activity relationships for the two classes of amphiphilic peptoid SP mimics under study. We propose to do this by varying key structural features and performing detailed studies of the effects on surface activity, in parallel with Molecular Dynamics simulations. For SP-C mimics, we will study the effects of hydrophobic helix length, side chain chemistry and overall helicity, and will also mimic the palmitoylation of natural SP-C. Proposed SP-B mimics will have increasingly protein-like sequences and side chain chemistries, and we will test the hypothesis that dimerization will improve their activity. We will carry out in vitro studies of peptoid-containing surfactant using CD, pulsating bubble surfactometry, a Langmuir trough/Wilhelmy surface balance, fluorescence microscopy, unilamellar vesicles, and X-ray reflectivity/diffraction to map out structure-activity relationships and study peptoid-lipid interactions. We will investigate surfactant formulations containing mimics of both SPs, and we will study the bicompatibility and in vivo efficacy of peptoid surfactants with lung epithelial cells and animal models of RDS.

描述（由申请人提供）：使用一种有效且低成本的仿生肺表面活性物质（LS）替代品可以更好、更广泛地治疗几种呼吸系统疾病和紊乱。在目前的医疗实践中，LS替代品（主要用于治疗新生儿呼吸窘迫综合征）来自动物肺部，价格昂贵，并且存在病毒传播和免疫反应的风险。我们建议继续开发一类基于聚n -取代甘氨酸（类肽）的肺表面活性蛋白的新型功能模拟物，这是一种在固相上合成的序列特异性异聚物，类似于肽。类肽具有蛋白酶抗性，通过适当的序列设计可以形成稳定的螺旋二级结构，抵抗非特异性聚集。在过去的3.5年里，我们已经创建和研究了两种不同的新型螺旋型两亲肽类低聚物，它们的序列和结构与(1)SP-B（残基1-25）和(2)SP-C（残基5-32）相似。体外生物物理研究表明，这些基于肽的SP模拟物在类ls脂质膜中的表面活性表明，每一类模拟物的最佳设计与它们被设计取代的天然肽相似。虽然初步结果非常有希望，但要开发基于肽的SP模拟物以用于临床有用的仿生LS替代品，还有很多工作要做。我们现在必须对正在研究的两类两亲性肽类SP模拟物的结构-活性关系有更深入的了解。我们建议通过改变关键的结构特征和对表面活性的影响进行详细的研究来做到这一点，同时进行分子动力学模拟。对于SP-C模拟物，我们将研究疏水螺旋长度、侧链化学和整体螺旋度的影响，并将模拟天然SP-C的棕榈酰化。提出的SP-B模拟物将具有越来越多的蛋白质样序列和侧链化学，我们将测试二聚化将提高其活性的假设。我们将使用CD、脉动气泡表面测定法、Langmuir槽/Wilhelmy表面平衡法、荧光显微镜、单层囊泡和x射线反射/衍射法对含肽类表面活性剂进行体外研究，以绘制结构-活性关系并研究肽类-脂质相互作用。我们将研究含有这两种SPs模拟物的表面活性剂配方，并研究类肽表面活性剂与肺上皮细胞和RDS动物模型的双相容性和体内疗效。

项目成果

Helical peptoid mimics of lung surfactant protein C.

• DOI: 10.1016/j.chembiol.2003.10.008
• 发表时间: 2003-11
• 期刊: Chemistry & biology
• 作者: Cindy W. Wu;Shannon L. Seurynck;Ka Yee C. Lee;A. Barron

Lipid composition greatly affects the in vitro surface activity of lung surfactant protein mimics.

脂质组成极大地影响肺表面活性蛋白模拟物的体外表面活性。

• DOI: 10.1016/j.colsurfb.2007.01.001
• 发表时间: 2007
• 期刊: Colloids and surfaces. B, Biointerfaces
• 作者: Seurynck-Servoss,ShannonL;Brown,NathanJ;Dohm,MichelleT;Wu,CindyW;Barron,AnneliseE
• 通讯作者: Barron,AnneliseE

Biomimicry of surfactant protein C.

• DOI: 10.1021/ar800058t
• 发表时间: 2008-10
• 期刊: ACCOUNTS OF CHEMICAL RESEARCH
• 影响因子: 18.3
• 作者: Brown, Nathan J.;Johansson, Jan;Barron, Annelise E.
• 通讯作者: Barron, Annelise E.

Close mimicry of lung surfactant protein B by "clicked" dimers of helical, cationic peptoids.

• DOI: 10.1002/bip.21309
• 发表时间: 2009
• 期刊: BIOPOLYMERS
• 影响因子: 2.9
• 作者: Dohm, Michelle T.;Seurynck-Servoss, Shannon L.;Seo, Jiwon;Zuckermann, Ronald N.;Barron, Annelise E.
• 通讯作者: Barron, Annelise E.

Intracellular biomass flocculation as a key mechanism of rapid bacterial killing by cationic, amphipathic antimicrobial peptides and peptoids.

• DOI: 10.1038/s41598-017-16180-0
• 发表时间: 2017-12-01
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Chongsiriwatana NP;Lin JS;Kapoor R;Wetzler M;Rea JAC;Didwania MK;Contag CH;Barron AE
• 通讯作者: Barron AE