Formation of Twisted β‐Sheet Tapes from a Self‐Complementary Peptide Based on Novel Pillararene‐GCP Host–Guest Interaction with Gene Transfection Properties. Issue 39 (12th June 2018)
- Record Type:
- Journal Article
- Title:
- Formation of Twisted β‐Sheet Tapes from a Self‐Complementary Peptide Based on Novel Pillararene‐GCP Host–Guest Interaction with Gene Transfection Properties. Issue 39 (12th June 2018)
- Main Title:
- Formation of Twisted β‐Sheet Tapes from a Self‐Complementary Peptide Based on Novel Pillararene‐GCP Host–Guest Interaction with Gene Transfection Properties
- Authors:
- Hu, Xiao‐Yu
Ehlers, Martin
Wang, Tingting
Zellermann, Elio
Mosel, Stefanie
Jiang, Hao
Ostwaldt, Jan‐Erik
Knauer, Shirley K.
Wang, Leyong
Schmuck, Carsten - Abstract:
- Abstract: Small peptides capable of assembling into well‐defined nanostructures have attracted extensive attention due to their interesting applications as biomaterials. This work reports the first example of a pillararene functionalized with a guanidiniocarbonyl pyrrole (GCP)‐conjugated short peptide segment. The obtained amphiphilic peptide 1 spontaneously self‐assembles into a supramolecular β‐sheet in aqueous solution based on host–guest interaction between pillararene and GCP unit as well as hydrogen‐bonding between the peptide strands. Interestingly, peptide 1 at low concentration shows transitions from small particles to "pearl necklace" assemblies, and finally to branched fibers in a time‐dependent process. At higher concentration, it directly assembles into twisted β‐sheet tapes. Notably, without pillararene moiety, the control peptide A forms α‐helix structure with morphology changing from particles to bamboo‐like assemblies depending on concentration, indicating a significant role of the pillararene‐GCP host‐guest interaction for the secondary structure formation. Moreover, peptide 1 can serve as an efficient gene transfection vector. Abstract : A novel pillararene functionalized with a GCP‐conjugated short peptide segment can self‐assemble into a supramolecular β‐sheet in aqueous solution based on host–guest interaction between pillararene and GCP unit as well as hydrogen‐bonding between the peptide strands. Notably, without a pillararene moiety, theAbstract: Small peptides capable of assembling into well‐defined nanostructures have attracted extensive attention due to their interesting applications as biomaterials. This work reports the first example of a pillararene functionalized with a guanidiniocarbonyl pyrrole (GCP)‐conjugated short peptide segment. The obtained amphiphilic peptide 1 spontaneously self‐assembles into a supramolecular β‐sheet in aqueous solution based on host–guest interaction between pillararene and GCP unit as well as hydrogen‐bonding between the peptide strands. Interestingly, peptide 1 at low concentration shows transitions from small particles to "pearl necklace" assemblies, and finally to branched fibers in a time‐dependent process. At higher concentration, it directly assembles into twisted β‐sheet tapes. Notably, without pillararene moiety, the control peptide A forms α‐helix structure with morphology changing from particles to bamboo‐like assemblies depending on concentration, indicating a significant role of the pillararene‐GCP host‐guest interaction for the secondary structure formation. Moreover, peptide 1 can serve as an efficient gene transfection vector. Abstract : A novel pillararene functionalized with a GCP‐conjugated short peptide segment can self‐assemble into a supramolecular β‐sheet in aqueous solution based on host–guest interaction between pillararene and GCP unit as well as hydrogen‐bonding between the peptide strands. Notably, without a pillararene moiety, the GCP‐conjugated control peptide A forms a supramolecular α‐helix. Moreover, the amphiphilic peptide studied can achieve intracellular DNA delivery and gene transfection. … (more)
- Is Part Of:
- Chemistry. Volume 24:Issue 39(2018)
- Journal:
- Chemistry
- Issue:
- Volume 24:Issue 39(2018)
- Issue Display:
- Volume 24, Issue 39 (2018)
- Year:
- 2018
- Volume:
- 24
- Issue:
- 39
- Issue Sort Value:
- 2018-0024-0039-0000
- Page Start:
- 9754
- Page End:
- 9759
- Publication Date:
- 2018-06-12
- Subjects:
- host–guest interaction -- peptides -- pillararene -- self-assembly -- supramolecular chemistry
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201801315 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10508.xml