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GlycoDelete Part of the Protein Expression Technology Toolbox by VIB Koen Tyberghein, PhD BD manager, VIB Contact: [email protected] BPI 2020 Confidential

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GlycoDelete

Part of the Protein Expression Technology Toolbox by VIB

Koen Tyberghein, PhD

BD manager, VIB

Contact: [email protected]

BPI 2020

Confidential

Towards next-gen biopharmaceuticalsProprietary eukaryotic cell-based glyco-engineering toolbox for next-generation biopharmaceuticals

o Biobetters

o Improved pharmaceuticals (e.g. ADC’s)

Enabling tools for structural & functional analysis of challenging target proteins

Broad IP portfolio & extensive know-howo Protein glycosylation engineering: 8 patent families

o Protein expression: 2 patent families

Expanding strategic partnership base

Confidential

Heterogeneous N-glycosylation

• N-glycosylation on therapeutic proteins

o Protein purification issues

o Process reproducibility problems

o Variable therapeutic effect

o Disadvantages of engineered proteins or enzymatic approaches

Confidential

Glyco-engineering platform

Next-generation biopharmaceuticals

Proprietary glyco-engineering & proteinexpression technologies

Purification methods

Protein expression toolbox• Soluble proteins vs.

membrane proteins• Expression yield• Temporal/spatial expression

Protein analytics

EfficacyConvenienceCost

Next-gen biotherapeutics

Innovativevaccines

Glyco-engineering toolbox• Simple human N-glycans• No mucin-type O-

glycosylation

Glyco-expression systems• Mammalian (HEK293, CHO)• Yeast (Pichia pastoris)• Plants

Site-specific conjugationtechnologies• Coupling of functional

moieties (toxins, half-life extension, …)

GlycoDelete: the basic concept

Glycosylation in WT eukaryotic cells

Glycosylation in GlycoDelete cells

Confidential

Overview of glyco-expression systems

Glycoengineering N-glycans O-glycans N-glycan effect

Wild type HEK293s

• heterogenic N- and O-glycans

• not function/PK optimized

GlycoDelete• well defined short N-

glycans• heterogeneous O-glycans

GlycoDoubleDelete• 1 possible N-glycan

structure• no O-glycans

GlycoDoubleDelete+Galactose

• LacNAc N-glycans for site specific coupling

• no O-glycans

Mammalian cell expression systems (HEK293, CHO)

Protein Class #

mAb 15

Viral proteins 11

Enzymes 6

Cytokines 6

Membrane proteins 6

Nanobodies 5

Antigen 1

Fc fusion 1

Total 51

Pichia technologies

Glycoengineering N-glycans N-glycan effect

Wild type Pichia pastoris

• high mannose structures, • rapid clearance• potentially immunogenic

GlycoSwitch• contaminating high mannose

structures • potentially immunogenic

GlycoSwitch followed by clean-up

• no contaminating structures • no influence on cell growth

GlycoDelete (+ GalT)

• very homogeneous glycans • starting point for chemical coupling

P

P

P

P

(+ )

Glyco-engineered biotherapeutics

Optimized biologics by glyco-engineeringGlycoDelete hIgG1

Homogeneity PharmacokineticsADCC

Fc RI receptor affinity Fc RIIa receptor affinity Fc RIIb receptor affinity

Nature Biotechnology 32, 485–489 (2014)

Glyco-engineered glycan-conjugation

• Single domain antibodies as case study

• Targeted introduction of N-linked glycans in VHH scaffold

Glyco-conjugation strategiesWO/2018/206734

Glycan-specific (site selective) conjugation

GBP-R86N(1 N-glyc. site)

Periodate-based

Glyco-conjugation strategy

Galactose-oxidase based Glyco-conjugation

strategy

Structural biology

Enabling tools for structural & functional analysis of challenging target proteins

• Enhanced membrane protein expression

ACS Synth. Biol. 5, 1070-1075 (2016)

21 June 2019Enabling tools for structural & functional analysis of challenging target proteins

•WO 2013/107905:

“A host cell comprising a first exogenous nucleic acid sequence encoding amembrane protein and a second exogenous nucleic acid encoding ananobody that specifically binds to an extracellular or an intracellularconformational epitope of said membrane protein, each under the controlof a promoter.“

Enabling tools for structural & functional analysis of challenging target proteins

• Crystal structure of the hCSF-1:CSF-1RD1–D3 ternary complex

Structure 23, 1–11 (2015)

IP

GlycoDelete basic patentWO2010/015722

IP strategy

Antibodies in GDWO 2015/032899

GlycoDoubleDeleteWO2017/005925

Membrane proteins in GDWO2013/107905

GlycoSwitch + endoT cleanupWO 2017/191208

Glyco-engineered Ig domains WO/2018/206734

High LacNAc in GDWO 2019/053145

High SiaLacNAc in GDWO 2019/053147

PLATFORM DEVELOPMENTS & TECHNOLOGY BUILDING

PRODUCT DEVELOPMENTS

Glyco-engineered vaccinsIn preparation

Confidential

2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019

Confidential

SUMMARY: Protein glycosylation engineering, technology validation

GlycoDelete in mammalian cellsNature Biotechnology 32, 485–489 (2014)GlycoDelete in plant cellsNature Biotechnology 33, 1135-7 (2015)GlycoDelete in Pichia pastorisIn preparation

Structure determination of target - Structure 23, 1–11, (2015)Production of membrane receptor - ACS Synth. Biol. 5, 1070-1075 (2016)

Production and glycan profiling of biopharmaceuticals (industry) – independently validated by 3 pharma companies, of which two now hold a non-exclusive license. One food tech company holds a non-excl. license as well.

Structure determination of challenging target proteins – validated by # structural biology labs

Technology

High impact papers

Externalvalidation

Strong IPBroad patent protection on glyco-engineered cells, and on products and applications derived thereof.

8 patent families, 3 granted patents including in US & EP

• Monoclonal Abs• Ab fragments• Membrane receptors

Different proteinclasses

• Growth factors• Enzymes• Cytokines• Hormones

Partnership opportunitiesPlatform driven or target-based

Strategic co-development partnerships

• Novel therapeutic modalities(ADCs, …)

• Improved biotherapeutics

• Bioactivity, bioavailability, immune effector functions, selectivity, …

• Target antibody discovery

• Other

License deals

• Cell line development

• mammalian, Pichia, plants

• manufacturing of biopharmaceuticals

• Enabling tools for structural& functional analysis of challenging target proteins

• Other

Contact: E - [email protected] - +32 498 63 77 86