首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Self-Assembly of Fibronectin Mimetic Peptide-Amphiphile Nanofibers
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Self-Assembly of Fibronectin Mimetic Peptide-Amphiphile Nanofibers

机译:纤连蛋白模拟肽-两亲纳米纤维的自组装。

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摘要

Single-tailed peptide-amphiphiles have been shown to form nanofibers in solution and gel after screening of their electrostatic charges, and those containing cell-binding motifs are promising as tissue engineering scaffolds. A fibronectin-mimetic peptide sequence was developed, containing both the primary binding domain RGD and the synergy binding domain PHSRN, which has shown superior cell adhesion properties over simple RGD sequences and fibronectin in 2D culture. In order to test this sequence in a 3Denvironment in the future, we have designed a C16 singletailed peptide-amphiphile, PR_g (with a peptide headgroup of GGGSSPHSRN(SG)5RGDSP), that forms nanofibers and a gel in solution without any screening of its positive charge. In this study, we characterized the self-assembly properties of the PR_g peptide-amphiphile via critical micelle concentration (CMC) measurements, circular dichroism (CD) spectroscopy, cryo-transmission electron microscopy (cryo-TEM), small angle neutron scattering (SANS), and rheology measurements. The CMC of the PR_g amphiphile was determined to be 38 μM. CD measurements showed that even though the peptide formed an unordered secondary structure, the peptide-amphiphile’s spectrum after aging resembled more the spectrum of an Rtβ protein. Cryo-TEM images of a 100 μMpeptide-amphiphile solution showed individual nanofibers with a diameter of approximately 10 nm and lengths on the order of several micrometers. Images taken at higher concentrations (1 mM) show a high degree of bundling among the nanofibers, and at even higher concentrations (3 and 4 mM) SANS measurements also indicated that the peptide-amphiphile formed rod-shaped structures in solution. The peptide-amphiphile gel was monitored by parallel-plate rheometry, and the elastic modulus (G0) was greater than the viscous modulus (G00), which indicates that PR_g forms a gel. The shear modulus for a 2 day old gel was measured to be approximately 500 Pa, which is within the modulus range for living tissue; thus, the PR_g gel shows potential as a possible scaffold for tissue engineering.
机译:已显示,单尾肽两亲物在筛选其静电荷后会在溶液和凝胶中形成纳米纤维,而那些含有细胞结合基序的肽有望成为组织工程支架。开发了纤连蛋白模拟肽序列,它既包含主要结合结构域RGD,又包含协同结合结构域PHSRN,在二维培养中已显示出比简单的RGD序列和纤连蛋白优越的细胞粘附特性。为了将来在3D环境中测试此序列,我们设计了C16单尾肽两亲物PR_g(具有GGGSSPHSRN(SG)5RGDSP的肽头基),可在溶液中形成纳米纤维和凝胶,而无需对其进行任何筛选正电荷。在这项研究中,我们通过临界胶束浓度(CMC)测量,圆二色性(CD)光谱,低温透射电子显微镜(cryo-TEM),小角中子散射(SANS)表征了PR_g肽-两亲物的自组装特性。 )和流变学测量。 PR_g两亲物的CMC被确定为38μM。 CD测量表明,即使肽形成了无序的二级结构,老化后肽-两亲物的光谱也更像Rtβ蛋白的光谱。 100μM肽-两亲溶液的低温TEM图像显示了直径约10 nm,长度约几微米的单个纳米纤维。在较高浓度(1 mM)下拍摄的图像显示出纳米纤维之间的高度束缚,甚至在较高浓度(3和4 mM)下,SANS测量也表明肽-两亲物在溶液中形成了棒状结构。通过平行板流变法监测肽-两亲性凝胶,并且弹性模量(G0)大于粘性模量(G00),这表明PR_g形成凝胶。测量了两天龄凝胶的剪切模量约为500 Pa,该剪切模量在活组织的模量范围内。因此,PR_g凝胶显示出可能作为组织工程的支架。

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