2016
DOI: 10.1039/c5ra23352f
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Comparative cell adhesion properties of cysteine extended peptide architectures

Abstract: This study presents the comparative cell attachment investigation of TAT and well-known RGD peptide modified surfaces.

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Cited by 6 publications
(7 citation statements)
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“… 64 The peak at 286.3 eV could be assigned to the carbon atoms of the C=O or C–N 65 , 66 or to the O=C—N. 64 , 67 The amide related peak at 288.08 eV, 67 , 68 observed only for the functionalized sample, confirms the presence of peptides.…”
Section: Resultsmentioning
confidence: 85%
“… 64 The peak at 286.3 eV could be assigned to the carbon atoms of the C=O or C–N 65 , 66 or to the O=C—N. 64 , 67 The amide related peak at 288.08 eV, 67 , 68 observed only for the functionalized sample, confirms the presence of peptides.…”
Section: Resultsmentioning
confidence: 85%
“…1−4 Various site-selective and/or chemoselective modifications of different amino acids of proteins were reported, including cysteine, 5−8 methionine, 9−12 lysine, 13−16 tyrosine, 17 tryptophan, 18 arginine, 19 etc. Thanks to thiol's high nucleophilicity, cysteine is widely utilized for selective modifications for various applications, including activity-based protein profiling (ABPP), 20 cell imaging, 21 covalent inhibitors, 22−25 and so on.…”
mentioning
confidence: 99%
“…Post translational modifications (PTMs) of proteins play key roles for diversified protein functions, which also creates interest in designing various synthetic methods to modify proteins. Various site-selective and/or chemoselective modifications of different amino acids of proteins were reported, including cysteine, methionine, lysine, tyrosine, tryptophan, arginine, etc. Thanks to thiol’s high nucleophilicity, cysteine is widely utilized for selective modifications for various applications, including activity-based protein profiling (ABPP), cell imaging, covalent inhibitors, and so on.…”
mentioning
confidence: 99%
“…Before cancer prevention and treatment, detecting cancer cells at an early stage by sensing their presence in the human body is essential [ 149 ]. In vitro cancer-cell detection based on the electrochemical method—which provides label-free, non-invasive, and non-destructive performance that could further support anticancer drug discovery—has emerged recently [ 120 , 139 , 140 , 141 , 142 , 143 , 150 , 151 ]. Angeline et al (2020) reported the electrical signal enhancement of stomach cancer cell (MKN-28) viability through the electrochemical detection method, which is then useful for drug screening applications [ 144 ].…”
Section: Electrochemical Biosensing For Highly Proliferative Cellsmentioning
confidence: 99%