Whole-Cell Biosensor with Tunable Limit of Detection Enables Low-Cost Agglutination Assays for Medical Diagnostic Applications.

Whole-cell biosensors can form the basis of affordable, easy-to-use diagnostic tests that can be readily deployed for point-of-care (POC) testing, but to date the detection of analytes such as proteins that cannot easily diffuse across the cell membrane has been challenging. Here we developed a novel biosensing platform based on cell agglutination using an E. coli whole-cell biosensor surface-displaying nanobodies which bind selectively to a target protein analyte. As a proof-of-concept, we show the feasibility of this design to detect a model analyte at nanomolar concentrations. Moreover, we show that the design architecture is flexible by building assays optimized to detect a range of model analyte concentrations using straightforward design rules and a mathematical model. Finally, we re-engineer our whole-cell biosensor for the detection of a medically relevant biomarker by the display of two different nanobodies against human fibrinogen and demonstrate a detection limit as low as 10 pM in diluted human plasma. Overall, we demonstrate that our agglutination technology fulfills the requirement of POC testing by combining low-cost nanobody production, customizable detection range and low detection limits. This technology has the potential to produce affordable diagnostics for field-testing in the developing world, emergency or disaster relief sites, as well as routine medical testing and personalized medicine.

[1]  Jamshid Tanha,et al.  Selection by phage display of llama conventional V(H) fragments with heavy chain antibody V(H)H properties. , 2002, Journal of immunological methods.

[2]  Aldo Roda,et al.  SENSITIVE DETERMINATION OF URINARY MERCURY(II) BY A BIOLUMINESCENT TRANSGENIC BACTERIA-BASED BIOSENSOR , 2001 .

[3]  G. Bodelón,et al.  Selection of Single Domain Antibodies from Immune Libraries Displayed on the Surface of E. coli Cells with Two β-Domains of Opposite Topologies , 2013, PloS one.

[4]  G. Georgiou,et al.  Antibody affinity maturation using bacterial surface display. , 1998, Protein engineering.

[5]  A. Bobylev,et al.  A kinetic model of the agglutination process. , 1992, Mathematical biosciences.

[6]  C. Borrebaeck,et al.  Antibodies in diagnostics - from immunoassays to protein chips. , 2000, Immunology today.

[7]  R. Roovers,et al.  High affinity nanobodies against human epidermal growth factor receptor selected on cells by E. coli display , 2016, mAbs.

[8]  J. D. den Dunnen,et al.  Reliable and controllable antibody fragment selections from Camelid non-immune libraries for target validation. , 2006, Biochimica et biophysica acta.

[9]  J. L. Ortega-Vinuesa,et al.  A review of factors affecting the performances of latex agglutination tests , 2001, Journal of biomaterials science. Polymer edition.

[10]  Kendrick B. Turner,et al.  Hydroxylated polychlorinated biphenyl detection based on a genetically engineered bioluminescent whole-cell sensing system. , 2007, Analytical chemistry.

[11]  T. Gotoda,et al.  Diagnostic Accuracy of Latex Agglutination Turbidimetric Immunoassay in Screening Adolescents for Helicobacter pylori Infection in Japan , 2018, Digestion.

[12]  Douglas K. Martin,et al.  Top ten biotechnologies for improving health in developing countries , 2002, Nature Genetics.

[13]  E. Morse,et al.  Determination of fibrinogen in plasma. , 1978, Annals of clinical and laboratory science.

[14]  B. de Geus,et al.  Induction of immune responses and molecular cloning of the heavy chain antibody repertoire of Lama glama. , 2000, Journal of immunological methods.

[15]  L. Rocha,et al.  Development of a Rapid Agglutination Latex Test for Diagnosis of Enteropathogenic and Enterohemorrhagic Escherichia coli Infection in Developing World: Defining the Biomarker, Antibody and Method , 2014, PLoS neglected tropical diseases.

[16]  Xinbin Chen,et al.  Mutant p53 exerts a dominant negative effect by preventing wild-type p53 from binding to the promoter of its target genes , 2004, Oncogene.

[17]  J. Horswell,et al.  Use of biosensors to screen urine samples for potentially toxic chemicals. , 2003, Journal of analytical toxicology.

[18]  Sonja Billerbeck,et al.  A modular yeast biosensor for low-cost point-of-care pathogen detection , 2017, Science Advances.

[19]  L. Looger,et al.  Computational design of receptor and sensor proteins with novel functions , 2003, Nature.

[20]  V. Salema,et al.  Escherichia coli surface display for the selection of nanobodies , 2017, Microbial biotechnology.

[21]  S. Muyldermans,et al.  Surface display of a single-domain antibody library on Gram-positive bacteria , 2012, Cellular and Molecular Life Sciences.

[22]  M. Cowie National Institute for Health and Care Excellence. , 2015, European heart journal.

[23]  Eduardo Cortón,et al.  Quantitative Immunoassays with Labels , 2004 .

[24]  H. de Haard,et al.  Properties, production, and applications of camelid single-domain antibody fragments , 2007, Applied Microbiology and Biotechnology.

[25]  S. Campuzano,et al.  Disposable amperometric magnetoimmunosensors using nanobodies as biorecognition element. Determination of fibrinogen in plasma. , 2014, Biosensors & bioelectronics.

[26]  S. Thompson,et al.  Production of C-reactive protein and risk of coronary events in stable and unstable angina , 1997, The Lancet.

[27]  Richard J. R. Kelwick,et al.  A protease-based biosensor for the detection of schistosome cercariae , 2016, Scientific Reports.

[28]  G. Lowe,et al.  Plasma fibrinogen. , 2004, Annals of clinical biochemistry.

[29]  Kelly A. Schwarz,et al.  Modular Extracellular Sensor Architecture for Engineering Mammalian Cell-based Devices , 2014, ACS synthetic biology.

[30]  G. Neumann,et al.  Influenza A virus isolation, culture and identification , 2014, Nature Protocols.

[31]  Christopher A. Voigt,et al.  Automated Design of Synthetic Ribosome Binding Sites to Precisely Control Protein Expression , 2009, Nature Biotechnology.

[32]  W. Lubitz,et al.  The bacterial ghost platform system , 2010, Bioengineered bugs.

[33]  Ric,et al.  CARDIAC TROPONIN T LEVELS FOR RISK STRATIFICATION IN ACUTE MYOCARDIAL ISCHEMIA , 2000 .

[34]  F. Harrell,et al.  Cardiac troponin T levels for risk stratification in acute myocardial ischemia. GUSTO IIA Investigators. , 1996, The New England journal of medicine.

[35]  Cleo Kontoravdi,et al.  Whole‐cell Escherichia coli lactate biosensor for monitoring mammalian cell cultures during biopharmaceutical production , 2017, Biotechnology and bioengineering.

[36]  G. Lowe,et al.  Guidelines on fibrinogen assays , 2003, British journal of haematology.

[37]  J. Crowley,et al.  Prevalence of prostate cancer among men with a prostate-specific antigen level < or =4.0 ng per milliliter. , 2004, The New England journal of medicine.

[38]  Weiling Fu,et al.  Quantitative Determination of Fibrinogen of Patients with Coronary Heart Diseases through Piezoelectric Agglutination Sensor , 2010, Sensors.

[39]  Serge Muyldermans,et al.  Nanobodies: natural single-domain antibodies. , 2013, Annual review of biochemistry.

[40]  V. Salema,et al.  Characterization of nanobodies binding human fibrinogen selected by E. coli display. , 2016, Journal of biotechnology.

[41]  M. Leinonen,et al.  The latex agglutination test for the diagnosis of meningococcal and haemophilus influenzae meningitis. , 1977, Scandinavian journal of infectious diseases.

[42]  S. S. Olmsted,et al.  Requirements for high impact diagnostics in the developing world , 2006, Nature.

[43]  M. Cavallari Rapid and Direct VHH and Target Identification by Staphylococcal Surface Display Libraries , 2017, International journal of molecular sciences.

[44]  G. Georgiou,et al.  Production and fluorescence-activated cell sorting of Escherichia coli expressing a functional antibody fragment on the external surface. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[45]  Stefan Dübel,et al.  Targeting Recombinant Antibodies to the Surface of Escherichia coli: Fusion to a Peptidoglycan Associated Lipoprotein , 1991, Bio/Technology.

[46]  Chad A. Mirkin,et al.  Drivers of biodiagnostic development , 2009, Nature.

[47]  S. Belkin,et al.  Where microbiology meets microengineering: design and applications of reporter bacteria , 2010, Nature Reviews Microbiology.

[48]  M. Assicot,et al.  High serum procalcitonin concentrations in patients with sepsis and infection , 1993, The Lancet.

[49]  M. Leinonen,et al.  Latex agglutination test for screening of Haemophilus influenzae type b carriers , 1987, Journal of clinical microbiology.

[50]  Franck Molina,et al.  Detection of pathological biomarkers in human clinical samples via amplifying genetic switches and logic gates , 2015, Science Translational Medicine.