Selected peptides and hybrid peptides (combinations of peptide sequences with organic moieties in a single molecule) self-assemble to form pores, channels and tubules. The assemblies occur in a variety of motifs. Various physiological functions, such as ion transport through cell membranes, and physical functions, such as solubilizing difficult-to-dissolve molecules, are facilitated by the tubes that are formed by molecular assemblies. Examples from nature are the ionophores zervamicin and antiamoebin that transport K+ ions through cell membranes. In the area of the constriction of the hour-glass shaped channel in the ionophores, the channel becomes quite convoluted and contains the double-gating mechanism that controls the ion passage. The...
Tubular structures can be obtained in various elegant ways. Electrospinning is the electrostatic for...
We have designed a four-helix protein that is expected to tetramerize in the membrane to form an ion...
AbstractWe have designed a four-helix protein that is expected to tetramerize in the membrane to for...
In the last few years, significant advances have been made in the use of peptides as building blocks...
We have designed a four-helix protein that is expected to tetramerize in the membrane to form an ion...
Peptide nanotubes with filled and empty pores and close-packed structures are formed in closely re...
The crystallographic observation of a hydrophobic, empty channel (diameter 5.2 Å) in the peptide Boc...
Abstract: Pore-forming peptides are of interest due to their antimicrobial activity and ability to f...
We describe here a unique family of pore-forming anion-transporting peptides possessing a single-ami...
Organic nanotubes have been rapidly gaining attention for use in a wide range of applications relate...
AbstractA cylindrical transmembrane molecule is constructed by linking hydrophobic sites selected fr...
The microscopic properties of water in narrow pores are relevant to the function of ion channels and...
Transmembrane channels and pores have key roles in fundamental biological processes1 and in biotechn...
The design of peptides that assemble in membranes to form functional ion channels is challenging. Sp...
Self-assembled structures obtained from organic molecules have shown great potential for application...
Tubular structures can be obtained in various elegant ways. Electrospinning is the electrostatic for...
We have designed a four-helix protein that is expected to tetramerize in the membrane to form an ion...
AbstractWe have designed a four-helix protein that is expected to tetramerize in the membrane to for...
In the last few years, significant advances have been made in the use of peptides as building blocks...
We have designed a four-helix protein that is expected to tetramerize in the membrane to form an ion...
Peptide nanotubes with filled and empty pores and close-packed structures are formed in closely re...
The crystallographic observation of a hydrophobic, empty channel (diameter 5.2 Å) in the peptide Boc...
Abstract: Pore-forming peptides are of interest due to their antimicrobial activity and ability to f...
We describe here a unique family of pore-forming anion-transporting peptides possessing a single-ami...
Organic nanotubes have been rapidly gaining attention for use in a wide range of applications relate...
AbstractA cylindrical transmembrane molecule is constructed by linking hydrophobic sites selected fr...
The microscopic properties of water in narrow pores are relevant to the function of ion channels and...
Transmembrane channels and pores have key roles in fundamental biological processes1 and in biotechn...
The design of peptides that assemble in membranes to form functional ion channels is challenging. Sp...
Self-assembled structures obtained from organic molecules have shown great potential for application...
Tubular structures can be obtained in various elegant ways. Electrospinning is the electrostatic for...
We have designed a four-helix protein that is expected to tetramerize in the membrane to form an ion...
AbstractWe have designed a four-helix protein that is expected to tetramerize in the membrane to for...