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CellJammer® discovery technology

Overview Process
● Our Aim:
ProtAffin Biotechnologie AG has ProtAffin uses the CellJammer®
To develop novel anti-
developed the novel CellJammer® discovery technology to create protein-
inflammatory biologicals
discovery technology for developing based GAG antagonists. We use
by targeting endothelial
anti-inflammatory and other products. structural bioinformatics for rational
surface glycan structures
We will work with Pharma/Biotech design of mutants, followed by
for the first time.
companies to apply our technology to proprietary assays to select optimal
their targets of interest. therapeutics. We achieve an increase
in GAG-binding affinity, without
● Relevant Targets
Technology changing the specificity of GAG
Relevant targets share binding. Secondly, we “inactivate“ the
ProtAffin‘s co-Founder, Prof. Andreas target protein, e.g. by knocking-out the
property of binding to
Kungl is a leader in the field of GPCR activity of chemokines.
glycans (GAGs). Initial
protein-glycan interactions. Over the Following in vitro and cell-based
focus is on chemokines
last 10 years, it has been shown that characterisation, we work with
but with wider applications.
protein-glycan (i.e. Protein-GAG) partners to characterise the
interactions drive many acute and pharmacology of the proteins in ex
chronic inflammatory processes. vivo and in vivo disease models.
● Process
ProtAffin has developed the
Design and development CellJammer® discovery technology to Discovery
In vitro
studies
In vivo
models
Pre-clinical
development Phase I
Disease
indication

of protein-based GAG create proteins with improved binding IL-8


CellJammer™
PA04-001
I/R injury in transplant
RA, others

antagonists, taking 6 to disease-related GAGs, thereby Chemokine 2


CellJammer™
months from start to in
Various

acting as potent, targeted anti- PA05-008

vivo characterisation. inflammatory products (ref.1). Chemokine 3


CellJammer™
PA05-017
Various

Target 4
CellJammer™ Various
PA06-001

● Advantages Partners

Target Characterisation:
Undisclosed Various indications

Faster development of
specific therapeutics than
with glycan-based drugs, Advantages
easier manufacturing and A number of companies have
specificity more easily developed monoclonal antibodies to
achieved GAG-binding proteins. This
complication in target biology provides
Model of an IL-8 monomer bound to a the chance to create superior
● Business Model GAG oligosaccharide therapeutics to mAbs when dealing
ProtAffin works with Chemokines rely on protein-GAG with this significant class of complex
partners to co-develop interactions for efficiently driving proteins. ProtAffin offers a new, fast
therapeutics with usual cellular inflammation in diseases such track way to target protein-glycan
milestone payments and as ischemia/reperfusion injury and interactions, avoiding the need for
royalty entitlements rheumatoid arthritis. ProtAffin is complex carbohydrate chemistry and
initially applying its discovery expensive manufacturing scale-up.
technology to chemokines for the
● Collaborations development of anti-inflammatory References
products (ref. 2). 1) Gesselbauer & Kungl, Curr. Op. Mol.
We are currently Therap. 8, 521 (2006)
collaborating with leading 2) Potzinger et al., Biochem. Soc.
universities and are Transact. 34, 435 (2006)
seeking Pharma/Biotech
collaborations Contact: ProtAffin Biotechnologie AG
Impulszentrum Graz-West, Reininghausstrasse 13a
A-8020 Graz, Austria
Web: www.protaffin.com
Tel: +43 316 382 541
January 2008 E-mail: office@protaffin.com

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