4.8 Article

Phage-AgNPs complex as SERS probe for U937 cell identification

Journal

BIOSENSORS & BIOELECTRONICS
Volume 74, Issue -, Pages 398-405

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2015.05.073

Keywords

SERS; Phage display; U937 cells; Cell identification; Minimal residual disease

Funding

  1. Italian Ministry of Education, University and Research (MIUR) [PON02 00355]
  2. A.B.A.L. onlus Messina (Italy)

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The early diagnosis of malignancy is the most critical factor for patient survival and the treatment of cancer. In particular, leukemic cells are highly heterogeneous, and there is a need to develop new rapid and accurate detection systems for early diagnosis and monitoring of minimal residual disease. This study reports the utilization of molecular networks consisting of entire bacteriophage structure, displaying specific peptides, directly assembled with silver nanoparticles as a new Surface Enhanced Raman Spectroscopy (SERS) probe for U937 cells identification in vitro. A 9-mer pVIII M13 phage display library is screened against U937 to identify peptides that selectively recognize these cells. Then, phage clone is assembled with silver nanoparticles and the resulting network is used to obtain a SERS signal on cell-type specific molecular targets. The proposed strategy could be a very sensitive tool for the design of biosensors for highly specific and selective identification of hematological cancer cells and for detection of minimal residual disease in a significant proportion of human blood malignancy. (C) 2015 Elsevier B.V. All rights reserved.

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