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• W2014862968 abstract "Smaller engineered analogs of angiogenic cytokines may provide translational advantages, including enhanced stability and function, ease of synthesis, lower cost, and, most important, the potential for modulated delivery via engineered biomaterials. In order to create such a peptide, computational molecular modeling and design was employed to engineer a minimized, highly efficient polypeptide analog of the stromal cell–derived factor-1α (SDF) molecule. After removal of the large, central β-sheet region, a designed diproline linker connected the native N-terminus (responsible for receptor activation and binding) and C-terminus (responsible for extracellular stabilization). This yielded energetic and conformational advantages resulting in a small, low-molecular-weight engineered SDF polypeptide analog (ESA) that was shown to have angiogenic activity comparable to or better than that of recombinant human SDF both in vitro and in a murine model of ischemic heart failure." @default.
• W2014862968 created "2016-06-24" @default.
• W2014862968 creator A5004761665 @default.
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• W2014862968 date "2012-08-01" @default.
• W2014862968 modified "2023-10-16" @default.
• W2014862968 title "Re-Engineered Stromal Cell–Derived Factor-1α and the Future of Translatable Angiogenic Polypeptide Design" @default.
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• W2014862968 doi "https://doi.org/10.1016/j.tcm.2012.07.010" @default.
• W2014862968 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4155938" @default.
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