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QF-Pro

A patented FRET reagent kit that, combined with the Violet 3.0 benchtop FLIM system and QF-Pro Software, forms a time-domain FLIM-FRET platform for quantifying protein-protein interactions in tissue–converting "how much protein" into "is it engaged."

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Definition
QF-Pro is a patented FRETLoading... reagent kit developed by HAWK Biosystems for quantitative detection of protein-protein interactionsLoading... at molecular distances (1–10 nm). Read on the Violet 3.0Loading... benchtop FLIMLoading... system, the combined workflow forms a time-domain FLIM-FRET platform: by measuring donor fluorescence lifetimeLoading... changes rather than intensity, the system detects genuine molecular engagement in FFPE tissueLoading... sections–enabling functional biomarkerLoading... analysis compatible with standard clinical pathology workflows.
Technology Comparison: Coloc vs PLA vs QF-Pro
Primary
The QF-Pro Reagent Kit & Workflow
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QF-Pro Score: How FRET Efficiency Is Calculated
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Applications Beyond Oncology
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Related Segments
Violet 3.0: Benchtop FLIM Microscope
Related
1–10 nm detection range
True molecular engagement
Lifetime-based readout
Intensity-independent quantification
High-throughput acquisition
Automated ROI detection
Standard tissue compatibility
Clinical workflow integration

How QF-Pro Works

QF-Pro employs a two-site labeling approach using species-specific secondary antibodies conjugated to donor (ATTO488) and acceptor (Alexa594) chromophores. When the target proteins are within 1–10 nm–indicating true molecular engagement–energy transfers from the excited donor to the acceptor, reducing donor fluorescence lifetime.

The Violet 3.0Loading... benchtop FLIM system measures this lifetime reduction with high throughput. Unlike intensity-based methods, lifetime measurement is intrinsically ratiometric and remains accurate even when protein expression is low–precisely the clinical scenario where expression-based biomarkers fail.

Tyramide signal amplificationLoading... (TSA) is incorporated to enhance acceptor chromophoreLoading... deposition, improving signal-to-noise ratios and enabling detection of sparse protein complexes in clinical tissue samples.

Clinical Evidence: See QF-Pro Applications & Clinical EvidenceLoading... for validated targets, cancer indications, and full citations.
Simplified

The Core Technology: QF-Pro combines FRET (detecting protein interactions at 1-10nm) with FLIM (measuring fluorescence lifetime for quantitative readout).

In Practice: Two antibodies labeled with donor and acceptor fluorophores bind target proteins. If the proteins are interacting (close enough for FRET), the donor lifetime changes. This change is measured and quantified.

Why Lifetime-Based FRET Is Uniquely Suited

Proximity-specific: Signal arises only from interacting molecules within 1–10 nm. Proteins merely colocalized in the same cellular region generate no FRET signal, eliminating the false positives that plague proximity ligation and colocalizationLoading... assays.

Intensity-independent: Fluorescence lifetime is an intrinsic property of the chromophore. Low protein expression does not compromise accuracy–critically important for detecting biologically decisive PPIs at sparse immune synapses or in heterogeneous tumor microenvironments.

Quantitative and reproducible: FRET efficiencyLoading... is calculated using the standardized equation Ef = [1 - (τDAD)] × 100, providing continuous numerical output compatible with regulatory validation requirements for companion diagnosticsLoading....

FFPE-compatible: Operates on standard formalin-fixed paraffin-embedded tissue sections, enabling retrospective analysis of biobanked samples and integration with existing clinical pathology infrastructure.

For clinical evidence and validated applications, see QF-Pro Applications & Clinical EvidenceLoading...

Simplified

Key Advantages:

Proximity-specific: Only detects genuine interactions (1-10nm)

Intensity-independent: Works even when protein levels are low

Quantitative: Provides numbers, not just positive/negative

FFPE-compatible: Works with standard clinical samples

Explore QF-Pro Applications

QF-Pro has been validated across multiple cancer types and clinical contexts, with evidence published in peer-reviewed journals spanning 2014—2025.

Navigate validated indications (melanoma, breast, RCC, colorectal, lung), landmark findings (PD-1/PD-L1, PKB/Akt, CTLA-4/CD80), clinical applications, and the exploratory pipeline.

20 Validated Applications 13 Exploratory Targets 400+ Patients
Simplified

QF-Pro has validated clinical applications across multiple cancers and targets.

Explore all validated indications, landmark findings, and the development pipeline.

20 validated applications · 13 exploratory targets · 400+ patients studied

Expression-Based IHC
"How much protein is present?"
Measures abundance only
Misses low-expression engagement
QF-Pro FLIM-FRET
"Is the protein functionally engaged?"
Measures molecular interaction
Detects biology IHC cannot see

Clinical Validation Highlights

  • PD-1/PD-L1Loading... in melanoma and NSCLC: iFRETLoading...-measured interaction state directly correlated with overall survival, while PD-L1 expression alone did not predict patient outcome
  • PKB/Akt activationLoading... in breast and renal cell carcinoma: Oncoprotein activation state (measured by FRET efficiency) correlated with worsened patient outcome, whereas expression levels showed no predictive value
  • Inter- and intra-patient heterogeneity: Quantitative mapping reveals checkpoint engagement variability that expression-based methodsLoading... cannot capture
  • Workflow compatibility: Tissue preparation identical to routine IHCLoading...; automated acquisition reduces operator bias and enables reproducible quantification across institutions

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