“Click” Immobilization of a VEGF-Mimetic Peptide on Decellularized Endothelial Extracellular Matrix to Enhance Angiogenesis
Author(s) -
Lin Wang,
Meirong Zhao,
Siheng Li,
Uriel Joseph Erasquin,
Hao Wang,
Li Ren,
Changyi Chen,
Yingjun Wang,
Chengzhi Cai
Publication year - 2014
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/am501309d
Subject(s) - decellularization , extracellular matrix , angiogenesis , peptide , materials science , vascular endothelial growth factor , biophysics , extracellular , click chemistry , matrix (chemical analysis) , substrate (aquarium) , nanotechnology , microbiology and biotechnology , vegf receptors , biochemistry , chemistry , biology , cancer research , polymer chemistry , ecology , composite material
We show that coating of decellularized extracellular matrix (DC-ECM) on substrate surfaces is an efficient way to generate a platform mimicking the native ECM environment. Moreover, the DC-ECM can be modified with a peptide (QK) mimicking vascular endothelial growth factor without apparently compromising its integrity. The modification was achieved through metabolic incorporation of a "clickable" handle to DC-ECM followed by rapid attachment of the QK peptide with an azido tag using copper-catalyzed click reaction. The attachment of the QK peptide on to DC-ECM in this way further enhanced the angiogenic responses (formation of branched tubular networks) of endothelial cells.
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