6533b82cfe1ef96bd128e932

RESEARCH PRODUCT

In vivophage display: identification of organ-specific peptides using deep sequencing and differential profiling across tissues

Kārlis PleikoKristina PõšnograjevaMaarja HaugasPäärn PaisteAllan TobiKaarel KurmUna RiekstinaTambet Teesalu

subject

chemistry.chemical_classificationPhage displaybiologychemistryT7 phageIn vivoPeptideBiopanningComputational biologybiology.organism_classificationDeep sequencingDNA sequencingHoming (hematopoietic)

description

ABSTRACTIn vivophage display is widely used for identification of organ- or disease-specific homing peptides. However, the currentin vivophage biopanning approaches fail to assess biodistribution of specific peptide phages across tissues during the screen, thus necessitating laborious and time-consuming post-screening validation studies on individual peptide phages. Here, we adopted bioinformatics tools used for RNA sequencing for analysis of high throughput sequencing (HTS) data to estimate the representation of individual peptides during biopanningin vivo. The data fromin vivophage screen were analyzed using differential binding – relative representation of each peptide in the target organ vs. in a panel of control organs. Application of this approach in a model study using low-diversity peptide T7 phage library with spiked-in brain homing phage, demonstrated brain-specific differential binding of brain homing phage and resulted in identification of novel lung and brain specific homing peptides. Our study provides a broadly applicable approach to streamlinein vivopeptide phage biopanning and to increase its reproducibility and success rate.Graphic abstractIn vivophage display using differential binding approach

https://doi.org/10.1101/2020.07.01.181974