FUNCTION-FIRST PROTEIN DESIGN

Define function through reasoning.
Realize design through generation.

Therapeutic proteins, designed on demand.

Integrating biology, protein structure and cell state —
from understanding biology to designing therapeutic sequences.

LexicodonTHERAPEUTICS

01 / THE PARADIGM SHIFT

The next paradigm in protein design
starts with function.

01

Reason to understand

Integrate biological mechanisms, protein structure and cell state to expand how models reason about the biological world.

02

Generate with purpose

Turn biological understanding into design criteria. Guide generation with reasoning to jointly optimize binding and function.

03

Learn through experiment

Make every round of validation the starting point for the next improvement in model performance.

02 / LEXIFORGE CLOSED-LOOP INTELLIGENCE

From cell state
to therapeutic sequence.

LexiForge connects protein generation, functional prediction and active learning in a continuously improving loop.

01 / GENERATE

Protein generation

Design therapeutic sequences by working backwards from cell state.

02 / EVALUATE

Functional prediction

Simulate cell fate to read out functional responses such as activation, killing and exhaustion.

03 / LEARN

Active learning

Use wet-lab data to continually calibrate models and inform the next round of design.

03 / VALIDATION & SERVICES

Validated design. Ready for your next discovery.

82.9%

Wet-lab hit rate

PD-L1 target · 29/35 tested
One-shot de novo miniprotein binders

>95%

Expression success rate

100% expression for PD-L1 miniproteins
Over 90% expression for VHHs

0.879 nM

Best binding affinity

One-shot de novo generation
PD-L1 Miniprotein binder Kd

85×

DRY-LAB HARD FILTER

Dry-lab filter pass rate for de novo candidates

Relative to other models, including PXDesign and RF3; computational screening metric reported in the one-pager.

CASE STUDY

IFNAR2 Binder

VHH

44% Hit rate · 156 nM Kd

IFNAR2 VHH binder protein structure

CASE STUDY

PD-L1 Binder

Miniprotein · 100 AA

<1 nM Kd

PD-L1 miniprotein binder protein structure

OUR SERVICES

Bring validated capabilities to your research.

01 / DE NOVO BINDER DESIGN

De Novo Binder Design

Generate candidate binders through de novo sequence design for a specified target protein and binding site.

VHH / scFv / Antibody / Miniprotein

02 / AFFINITY ENGINEERING

Affinity Engineering

Use computational design and sequence optimization to increase or decrease the binding affinity of an existing protein for different applications.

Existing sequence → Computational design → Tuned affinity

04 / OUR NAME

Rooted in nature.
Written in sequence.

Our Chinese name, Lai Xi Cheng Xu, reflects a return to first principles and the laws of nature. “Cheng Xu” means forming a protein sequence and echoes the word for a computer program.

Protein function, programmed and refined.

05 / CAREERS

Help design the future of proteins.

We are seeking passionate candidates to join us in exploring AI-driven protein design and closed-loop experimentation.

OPEN ROLE

AI Protein Designer

To explore the role, send your CV and relevant project or research work.

Apply by email
careers@lexicodon.com