Bioconjugation of peptides using advanced nanomaterials to examine their interactions in 3D printed flow‐through device. Issue 3 (30th December 2015)
- Record Type:
- Journal Article
- Title:
- Bioconjugation of peptides using advanced nanomaterials to examine their interactions in 3D printed flow‐through device. Issue 3 (30th December 2015)
- Main Title:
- Bioconjugation of peptides using advanced nanomaterials to examine their interactions in 3D printed flow‐through device
- Authors:
- Michalek, Petr
Richtera, Lukas
Krejcova, Ludmila
Nejdl, Lukas
Kensova, Renata
Zitka, Jan
Kopel, Pavel
Heger, Zbynek
Adam, Vojtech
Kizek, Rene - Abstract:
- Abstract : Peptide–peptide interactions are crucial in the living cell as they lead to the formation of the numerous types of complexes. In this study, synthetic peptides containing 11 of cysteines (α‐domain of metallothionein (MT)) and sialic acid binding region (130‐loop of hemagglutinin (HA)) were employed. The aim of the experiment was studying the interactions between MT and HA‐derived peptides. For this purpose, fragments were tagged with cysteines at C ‐terminal part to serve as ligand sites for PbS and CuS quantum dots (QDs), and therefore these conjugates can be traced and quantified during wide spectrum of methods. As a platform for interaction, γ‐Fe2 O3 paramagnetic particles modified with tetraethyl orthosilicate and (3‐aminopropyl)triethoxysilane (hydrodynamic diameter 30–40 nm) were utilized and MT/HA interactions were examined using multi‐instrumental approach including electrochemistry, electrophoretic methods, and MALDI‐TOF/TOF mass spectrometry. It was found that peptides enter mutual creation of complexes, which are based on some of nonbonded interactions. The higher willingness to interact was observed in MT‐derived peptides toward immobilized HA. Finally, we designed and manufactured flow‐through electrochemical 3D printed device (reservoir volume 150 μL) and utilized it for automated analysis of the HA/MT metal labels. Under the optimal conditions, (deposition time and flow rate 80 s and 1.6 mL/min for CuS and 120 s and 1.6 mL/min PbS, respectively),Abstract : Peptide–peptide interactions are crucial in the living cell as they lead to the formation of the numerous types of complexes. In this study, synthetic peptides containing 11 of cysteines (α‐domain of metallothionein (MT)) and sialic acid binding region (130‐loop of hemagglutinin (HA)) were employed. The aim of the experiment was studying the interactions between MT and HA‐derived peptides. For this purpose, fragments were tagged with cysteines at C ‐terminal part to serve as ligand sites for PbS and CuS quantum dots (QDs), and therefore these conjugates can be traced and quantified during wide spectrum of methods. As a platform for interaction, γ‐Fe2 O3 paramagnetic particles modified with tetraethyl orthosilicate and (3‐aminopropyl)triethoxysilane (hydrodynamic diameter 30–40 nm) were utilized and MT/HA interactions were examined using multi‐instrumental approach including electrochemistry, electrophoretic methods, and MALDI‐TOF/TOF mass spectrometry. It was found that peptides enter mutual creation of complexes, which are based on some of nonbonded interactions. The higher willingness to interact was observed in MT‐derived peptides toward immobilized HA. Finally, we designed and manufactured flow‐through electrochemical 3D printed device (reservoir volume 150 μL) and utilized it for automated analysis of the HA/MT metal labels. Under the optimal conditions, (deposition time and flow rate 80 s and 1.6 mL/min for CuS and 120 s and 1.6 mL/min PbS, respectively), the results of peptide‐conjugated QDs were comparable with atomic absorption spectrometry. … (more)
- Is Part Of:
- Electrophoresis. Volume 37:Issue 3(2016)
- Journal:
- Electrophoresis
- Issue:
- Volume 37:Issue 3(2016)
- Issue Display:
- Volume 37, Issue 3 (2016)
- Year:
- 2016
- Volume:
- 37
- Issue:
- 3
- Issue Sort Value:
- 2016-0037-0003-0000
- Page Start:
- 444
- Page End:
- 454
- Publication Date:
- 2015-12-30
- Subjects:
- 3D printing -- Advanced materials -- Influenza -- Lab‐On‐a‐Chip -- Magnetic particle
Electrophoresis -- Periodicals
Electrophoresis -- Periodicals
541.372 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2683 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/elps.201500345 ↗
- Languages:
- English
- ISSNs:
- 0173-0835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3706.378000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2097.xml