Functional biosensing · R&D

Measure the effect.
Prioritize the decision.

SYGPeD™ turns a targeted biological interaction into a quantitative readout to compare, prioritize and confirm research candidates. The platform is primarily focused on immune-checkpoint R&D, with PD‑1/PD‑L1 as its reference module.

Immune checkpointsPD‑1/PD‑L110+ years R&DRUO
SYGPeD™ measurement principle
Same module, two comparable conditions
Conceptual
Conceptual SYGPeD measurement principle comparing reference and candidate conditions
Reference
Target → SYGPeD™ recognition interface
High signal
Same module · two comparable conditions
With candidate
Candidate perturbs target engagement
Lower signal

Target–interface engagement → quantitative signal. Conceptual illustration.

10+ yearsof research and development behind SYG technologies
PD‑1/PD‑L1reference immune-checkpoint module
Multi-targetexperimental validation across PD‑1/PD‑L1, HER2, EPO and cytokine models
RUOplatform and collaborations for research use
Why a functional readout?

Complement binding with a quantitative measure of the effect on the interaction under study.

SYGPeD™ provides a comparative assay-level readout to support candidate selection and organize confirmation steps.

BindingRecognition / affinity

Document candidate interaction with its target.

+
SYGPeD™Effect on the target interaction

Quantitatively compare candidate impact in the assay context.

Experimental workflow

Configure → Measure → Analyze

01

Configure

Target, assay conditions, controls, comparators and candidates.

Illustrative microplate
02

Measure

Acquire the signal with a readout system compatible with the module.

Illustrative plate reader
Indicative readout: 3–4 h*
03

Analyze

Normalize, compare and confirm by dose-response where appropriate.

Illustrative dose-response curve

* Indicative timing depends on module and protocol.

Experimental decisions

Fast screening followed by quantitative confirmation.

Single-concentration screening

Compare candidate series and prioritize hits for confirmation.

Illustrative screening chart

Dose-response

Compare profiles and estimate IC₅₀ when supported by experimental design and quality criteria.

Illustrative dose-response curve

Conceptual illustrations; demonstration charts are not experimental data unless explicitly stated.

Two complementary capabilities

Measure with SYGPeD™. Explore functional discovery with SYGPeP™.

RUO platform

SYGPeD™

Quantitative functional biosensing

Measure candidate effects on a targeted biological interaction.

  • Comparative screening
  • Dose-response and IC₅₀ when supported by design
  • Primary focus on immune checkpoints
  • Modularity supported by HER2, EPO and cytokine models
Explore SYGPeD™
Partner programs

SYGPeP™

Functional discovery & prioritization

Develop programs aimed at introducing a functional experimental criterion earlier in biomolecule prioritization.

  • VHHs, DARPins, peptides and additional formats depending on project
  • Partner-defined question and success criteria
  • Quantitative confirmation with SYGPeD™ where relevant
Discover SYGPeP™
Applications

Immune checkpoints first, with an architecture adaptable to additional targets.

PD‑1/PD‑L1 is the reference immune-checkpoint module. Experimental validation on HER2, EPO and several cytokine models supports the adaptability of the SYGPeD™ architecture.

Immune checkpoints

Screening and characterization of candidates targeting checkpoint–ligand interactions.

Multi-target validation

HER2, EPO and cytokine models illustrate the ability to configure the architecture around different biological targets.

New modules

New research directions are explored with hospital, academic and industry teams.

Working on a target, assay or candidate series?

A focused pilot can frame feasibility, controls and the experimental decision you need to make.

Discuss a pilot