Angewandte Chemie International Edition 2006, 45,
Form Determines Function
Nerve Regeneration: cyclopeptides imitate the structure and effect of the HNK-1 carbohydrate
Contact: Norbert Sewald, Universität Bielefeld (Germany)
Registered journalists may download the original article here:
Glycomimetic Cyclic Peptides Stimulate Neurite Outgrowth
Carbohydrates play an important role in a broad
spectrum of physiological as well as pathological processes. For example, polysaccharides on the surface of
tumor cells or pathogens are possible points of attack for therapeutic
drugs or vaccinations. However, the synthesis of carbohydrate-based
drugs or vaccines has proven to be very complex. In addition, these are
not easily absorbed into the body and decompose far too quickly.
Cyclopeptides (short ring-shaped protein chains) called glycomimetics,
which imitate polysaccharides in form and consequently in function,
could be a useful alternative. They are easy to produce, relatively
stable, and easily absorbed.
A team of researchers at the Universities of
Bielefeld and Hamburg (Germany)
has now produced cyclopeptides that imitate the HNK-1 carbohydrate from
human natural killer cells. HNK-1 is involved in many developmental
biological processes of the nervous system. It boosts motor neuron axon
growth, the growth of the fibers of muscle nerve cells. HNK-1 is found
along the routes used by nerve fibers after an injury to peripheral
As a first step, the researchers led by Norbert
Sewald (Bielefeld) and Melitta Schachner (Hamburg) combed through a very
large number of linear peptide chains with random amino acid sequences,
searching for peptides that could be recognized by HNK-1 antibodies.
Starting with the sequences of two such peptides, they synthesized a
series of different cyclic hexapeptides. Their trick was to replace one
L-amino acid in each cyclopeptide with its corresponding D-amino acid.
L-amino acids are the form that occurs in nature, D-amino acids are
their mirror image. Whereas a “normal” cyclic hexapeptide is very
flexible, constantly changing its spatial structure, a D-amino acid
component stabilizes one preferred conformation of the ring. The peptide
“presents” its functional groups of atoms in a predictable
three-dimensional arrangement that is further determined by the position
of the D-amino acid. The amino acid L-proline has a similar stabilizing
effect; so cyclic hexapeptides containing this unit were also tested.
Sewald and his team identified several interesting
candidates based on their tendency to bind to antibodies against HNK-1.
They then took a closer look at a few of these. Trials with motor neuron
cell cultures demonstrated that two of the mimetics tested did indeed
stimulate axon growth. Indeed, they were more effective than the linear
peptide chains the researchers started with. Structural analyses and computer simulations identified a particular spatial structure of
the cyclopeptides as being crucial to their effectiveness.
Substances able to support the regeneration of axons
after injuries could be a highly promising starting point for developing
a treatment of patients with spinal cord injuries. These new
cyclopeptides could be a step in the right direction.