Mass spectrometry reimagined for smarter, faster drug discovery

What is CARMS?

Collision Activated Rapid Mass Spectrometry (CARMS) is MassAffinity’s proprietary platform for rapidly and accurately identifying drug-target interactions in complex biological systems.

CARMS does what other methods don’t.

It works directly in native samples, with no protein purification, no assay development and no artificial environments.

This allows discovery teams to move faster, reduce risk and uncover interactions that might otherwise go undetected.

How CARMS works

From samples to hits at unmatched speed

CARMS accelerates drug screening into three key steps, all happening within a single instrument

Protein-drug mixtures are injected. The mass spectrometer selects protein-bound complexes while removing unbound molecules
The mass spectrometer applies energy to break apart the complexes, separating bound drug molecules from proteins.
The mass spectrometer detects only the drug molecules that were previously protein-bound, identifying hits.

How is CARMS different?

We don’t work around complexity, we cut through it.

Traditional hit identification requires purified proteins, custom assay development and biological systems that do not reflect real biology.

These steps are slow, costly, and often lead to missed or misleading results.

CARMS delivers faster, more accurate hit identification by removing the slowest and most limiting parts of traditional screening while preserving what matters most: real biological context.

What only CARMS can do

No protein purification required

CARMS works directly in cell lysates, eliminating the need for slow, complex protein preparation.

Built-in filtering eliminates false positives

Selective mass detection ensures only true binders are captured.

No custom assays required

There is no need to build custom assays — binding is detected directly using mass spectrometry.

High-throughput, even in complex samples

Highly multiplexed screening in lysates and mixtures without compromising biological fidelity.

Works in real biological context

CARMS captures interactions as they occur in native environments.

Delivers results in weeks, not months

By skipping purification and assay setup, CARMS dramatically reduces early-stage timelines.

Collision energy confirms true binding

Bound complexes are dissociated inside the mass spectrometer using controlled energy, revealing real interactions.

Accelerates discovery 10× over legacy workflows

CARMS technology products

CARMS Products for your discovery needs

Three focused products within the CARMS platform, tailored to support different phases and approaches in early discovery.

BinderMAP identifies true binders in record time

  • Validates AI or hypothesis-driven hits
  • Captures true binders
  • Works where custom assays cannot be developed
  • Reduces timelines and increases confidence

BinderMAP

TargetMAP finds hits faster for complex and undruggable targets

  • No protein purification required
  • Supports undruggable proteins
  • Screens in complex systems
  • Maintains native biological context

TargetMAP

PhenoMAP screens in native systems without needing a defined target

  • Deconvolutes mechanism of action
  • Ideal for exploratory discovery
  • Captures complexity of multifactorial diseases
  • Works directly in lysates

PhenoMAP

How our technology supports the drug discovery pipeline?

The starting point for smarter drug discovery

MassAffinity targets the earliest phase of drug discovery, where many programs stall due to undruggable targets, assay limitations or biological complexity.

Mass Affinity
BinderMAP
TargetMAP
PhenoMAP
Asset
Indication
Target ID
Target Validation
Hit ID
Hit-to-Lead
Preclinical Testing
Clinical Trials
Regulatory approval
Market Release