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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes a CRISPR-Cas-mediated, multianalyte synthetic urine biomarker test that enables point-of-care cancer diagnostics through the ex vivo analysis of tumor-associated protease activities.

Abstract

Creating synthetic biomarkers for the development of precision diagnostics has enabled detection of disease through pathways beyond those used for traditional biofluid measurements. Synthetic biomarkers generally make use of reporters that provide readable signals in the biofluid to reflect the biochemical alterations in the local disease microenvironment during disease incidence and progression. The pharmacokinetic concentration of the reporters and biochemical amplification of the disease signal are paramount to achieving high sensitivity and specificity in a diagnostic test. Here, a cancer diagnostic platform is built using one format of synthetic biomarkers: activity-based nanosensors carrying chemically stabilized DNA reporters that can be liberated by aberrant proteolytic signatures in the tumor microenvironment. Synthetic DNA as a disease reporter affords multiplexing capability through its use as a barcode, allowing for the readout of multiple proteolytic signatures at once. DNA reporters released into the urine are detected using CRISPR nucleases via hybridization with CRISPR RNAs, which in turn produce a fluorescent or colorimetric signal upon enzyme activation. In this protocol, DNA-barcoded, activity-based nanosensors are constructed and their application is exemplified in a preclinical mouse model of metastatic colorectal cancer. This system is highly modifiable according to disease biology and generates multiple disease signals simultaneously, affording a comprehensive understanding of the disease characteristics through a minimally invasive process requiring only nanosensor administration, urine collection, and a paper test which enables point-of-care diagnostics.

Introduction

Despite the significant effort to identify tumor biomarkers such as shed proteins and DNA, the cancer diagnostic field has been strained by their low abundance or rapid degradation in circulation1. As a complementary strategy, bioengineered synthetic biomarkers that selectively respond to disease features to generate amplified signals represent new avenues towards accurate and accessible diagnostics2,3. To aid detection, these synthetic biomarkers harness tumor-dependent activation mechanisms such as enzymatic amplification to produce analytes with improved signal-to-noise ratio

Protocol

All animal studies are approved by the Institutional Animal Care and Use Committee (IACUC) at the authors' institution. Standard animal care facilities including housing chambers, sterile hoods, anesthetization, and ethical endpoint euthanization are required to properly carry out these experiments. All experiments are conducted in compliance with institutional and national guidelines and supervised by the veterinarian staff at the institution. Female BALB/c mice, used for the experiments, are obtained from a commerc.......

Representative Results

Nominating protease-activated peptide substrates
To design sensors which will reflect changes in the proteolytic activity of the tissue, protease activity in the tissue is first characterized using a library of peptide probes13 (Figure 1). Fresh and frozen tissue samples can provide substantial information about the proteolytic activity of the tumor microenvironment by combining tissue samples with FRET probes designed to detect substrate cleava.......

Discussion

Presented here is a highly customizable platform for multiplexed cancer detection with a portable urine test that assesses disease-associated proteolytic activity using a minimally invasive injected sensor. When activated by tumor proteases, peptide substrate cleavage is amplified via DNA barcode release into the urine. The synthetic DNA reporters in a urine sample can be read out by a secondary CRISPR-Cas-mediated enzymatic amplification using fluorometric detection or a simple paper-based test. DNA barcoding i.......

Acknowledgements

This study was supported in part by a Koch Institute Support Grant number P30-CA14051 from the National Cancer Institute (Swanson Biotechnology Center), a Core Center Grant P30-ES002109 from the National Institute of Environmental Health Sciences, the Koch Institute's Marble Center for Cancer Nanomedicine, the Koch Institute Frontier Research Program via the Kathy and Curt Marble Cancer Research Fund, and the Virginia and D. K. Ludwig Fund for Cancer Research. A.E.V.H. is supported by an NIH-funded predoctoral training fellowship (T32GM130546). S.N.B. is a Howard Hughes Medical Institute Investigator. L.H. is supported by a K99/R00 Pathway to Independence Award fr....

Materials

NameCompanyCatalog NumberComments
10x NEB Buffer 2.1New England BiolabsB6002SVIAL
20-mer phosphorothioated DNA reporters with 3’-DBCO groupIDTCustom DNA
Agilent 1100 High Performance Liquid Chromatography system with Vydac 214TP510 C4 column AgilentHPLC
ÄKTA fast protein liquid chromatography (FPLC)GE HealthcareFPLC
Amicon ultracentrifuge tubes (MWCO = 10 kDa)EMD milliporeVarious volumes available
Azide-terminated PAPs with C-terminus cysteineCPC ScientificCustom peptide
crRNAs IDTSee Supplementary Table 1
Cryogenic transmission electron microscopyJEM-2100FJEOLcyroTEM
Cysteine terminated DNA-peptide conjugatesCPC ScientificCustom peptide
Dynamic light scattering (DLS)DLS
EnGen LbaCas12a (Cpf1), 100 µMNew England BiolabsM0653T
Experimental animalsTaconic BiosciencesBALB/cAnNTac6–8 weeks of age
gentleMACS C tubesMiltenyi Biotec130-093-237tissue homogenization
HybriDetect Universal Lateral Flow Assay KitMiltenyi BiotecMGHD 1
Matrix-assisted laser desorption/ionization–time of flight (MALDI–TOF) mass spectrometry BrukerMicroflex MALDI–TOF
MC26-Fluc cell lineKenneth K. Tanabe Laboratory, Massachusetts General Hospital
multivalent PEG (40 kDA, 8-arm) with maleimide-reactive groupJenKemA10020-1 / 8ARM(TP)-MAL-40K,1 g
Python, Version 3.9https://www.python.org/
Quant-iT OliGreen ssDNA Assay Kit and Quant-iT OliGreen ssDNA ReagentInvitrogenO11492ssDNA assay kit
ssDNA FAM-T10-Quencher and  FAM-T10-Biotin reporter substratesIDTCustom DNA
Superdex 200 Increase 10/300 GL columnGE HealthcareGE28-9909-44For FPLC
Tecan Infinite Pro M200 plate readerTecan
ThermoFisher Pierce BCA Protein Assay KitThermoFisher Scientific23225

References

  1. Soleimany, A. P., Bhatia, S. N. Activity-based diagnostics: an emerging paradigm for disease detection and monitoring. Trends Mol Med. 26 (5), 450-468 (2020).
  2. Muir, R. K., Guerra, M., Bogyo, M. M.

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