Department of Biomedical Engineering, University of Wisconsin, Madison, Wisconsin 53706, USA.
Langmuir. 2010 May 4;26(9):6449-56. doi: 10.1021/la1008208.
We have used the orthogonal carbodiimide condensation and copper-catalyzed azide-alkyne "click" cycloaddition (CuAAC) reactions to prepare self-assembled monolayers that present distinct peptides to stem cells in a bioinert background. The approach involved first forming mixed SAMs with three components: (i) an azide-terminated hexaethylene glycol alkanethiolate (HS-EG6-N3), (ii) a carboxylate-terminated hexaethylene glycol alkanethiolate (HS-EG6-COOH), and (iii) a triethylene glycol alkanethiolate (HS-EG3). An acetylene-bearing peptide and an amine-terminated peptide were then immobilized to these substrates using a "click" CuAAC reaction and a carbodiimide condensation reaction, respectively. Polarization-modulated infrared reflectance-absorbance spectroscopic analysis demonstrated formation of well-ordered, close-packed self-assembled monolayers (SAMs), chemoselective conjugation of amine-terminated peptides to surface carboxylate groups, and subsequent conjugation of acetylene-terminated peptides to the azide groups on SAMs. Varying the mole fraction of HS-EG6-N3, HS-EG6-COOH, and HS-EG3 during SAM formation allowed for control over the densities of each peptide on the substrate. Substrates presenting varying surface densities of RGESP (a nonfunctional peptide), RGDSP (a cell adhesion peptide), or TYRSRKY (a heparin/heparan sulfate-binding peptide) were then used to characterize the relationship between peptide surface density and human mesenchymal stem cell (hMSC) adhesion. Results demonstrate that RGESP does not influence RGDSP-mediated adhesion of hMSCs, which indicates that a second peptide with distinct bioactivity can be immobilized alongside RGDSP to characterize the influence of two peptides on hMSC behavior. Our results also demonstrate that RGDSP and TYRSRKY act synergistically to promote hMSC adhesion in the absence of serum. Interestingly, heparin sequestered by TYRSRKY inhibits cell adhesion on substrates presenting RGDSP = 0.1% and > or = 0.1% TYRSRKY or RGDSP = 1% and > or = 0.5% TYRSRKY. Taken together, these results indicate that two peptides can be controllably presented to stem cells on the same otherwise bioinert SAM substrate, and that multiple, distinct extracellular moieties act in concert to regulate hMSC adhesion.
我们使用正交碳二亚胺缩合和铜催化的叠氮化物-炔烃“点击”环加成(CuAAC)反应来制备自组装单层,在生物惰性背景下向干细胞呈现不同的肽。该方法涉及首先用三种成分形成混合 SAM:(i)末端叠氮化物的六乙二醇烷硫醇(HS-EG6-N3),(ii)末端羧酸盐的六乙二醇烷硫醇(HS-EG6-COOH)和(iii)三乙二醇烷硫醇(HS-EG3)。然后使用“点击”CuAAC 反应和碳二亚胺缩合反应将带有乙炔的肽和末端胺的肽分别固定到这些底物上。偏振调制红外反射吸收光谱分析表明形成了有序的、紧密堆积的自组装单层(SAM),末端胺的肽与表面羧酸盐基团的化学选择性偶联,以及随后的乙炔末端的肽与 SAM 上的叠氮基团的偶联。在 SAM 形成过程中改变 HS-EG6-N3、HS-EG6-COOH 和 HS-EG3 的摩尔分数,可以控制底物上每种肽的密度。然后使用呈现不同 RGESP(无功能肽)、RGDSP(细胞粘附肽)或 TYRSRKY(肝素/硫酸乙酰肝素结合肽)表面密度的底物来表征肽表面密度与人间充质干细胞(hMSC)粘附之间的关系。结果表明,RGESP 不影响 RGDSP 介导的 hMSC 粘附,这表明可以与 RGDSP 一起固定具有不同生物活性的第二种肽,以表征两种肽对 hMSC 行为的影响。我们的结果还表明,RGDSP 和 TYRSRKY 在没有血清的情况下协同促进 hMSC 粘附。有趣的是,被 TYRSRKY 隔离的肝素抑制在呈现 RGDSP=0.1%和>或=0.1%TYRSRKY 或 RGDSP=1%和>或=0.5%TYRSRKY 的底物上的细胞粘附。总的来说,这些结果表明可以在相同的生物惰性 SAM 底物上将两种肽可控地呈现给干细胞,并且多个不同的细胞外部分共同作用以调节 hMSC 粘附。