Synthesis and evaluation of the biostability and cell compatibility of novel conjugates of nucleobase, peptidic epitope, and saccharide

This article reports the synthesis of a new class of conjugates containing a nucleobase, a peptidic epitope, and a saccharide and the evalution of their gelation, biostability, and cell compatibility. We demonstrate a facile synthetic process, based on solid-phase peptide synthesis of nucleopeptides...

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Veröffentlicht in:Beilstein journal of organic chemistry 2015-08, Vol.11 (1), p.1352-1359
Hauptverfasser: Yuan, Dan, Du, Xuewen, Shi, Junfeng, Zhou, Ning, Baoum, Abdulgader Ahmed, Al Footy, Khalid Omar, Badahdah, Khadija Omar, Xu, Bing
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Sprache:eng
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Zusammenfassung:This article reports the synthesis of a new class of conjugates containing a nucleobase, a peptidic epitope, and a saccharide and the evalution of their gelation, biostability, and cell compatibility. We demonstrate a facile synthetic process, based on solid-phase peptide synthesis of nucleopeptides, to connect a saccharide with the nucleopeptides for producing the target conjugates. All the conjugates themselves (1-8) display excellent solubility in water without forming hydrogels. However, a mixture of 5 and 8 self-assembles to form nanofibers and results in a supramolecular hydrogel. The proteolytic stabilities of the conjugates depend on the functional peptidic epitopes. We found that TTPV is proteolytic resistant and LGFNI is susceptible to proteolysis. In addition, all the conjugates are compatible to the mammalian cells tested.
ISSN:1860-5397
1860-5397
DOI:10.3762/bjoc.11.145