| Title: | Whole-cell biopanning with a synthetic phage display library of nanobodies enabled the recovery of follicle-stimulating hormone receptor inhibitors |
|---|
| Authors: | ID Crepin, Ronan, Institut Curie (Author)
ID Veggiani, Gianluca, Institut Curie (Author)
ID Djender, Selma, Institut Curie (Author)
ID Beugnet, Anne, Institut Curie (Author)
ID Planeix, Francois, Institut Curie (Author)
ID Pichon, Christophe, Institut Curie (Author)
ID Moutel, Sandrine, Institut Curie (Author)
ID Amigorena, Sebastian, Institut Curie (Author)
ID Pérez, Franck, Institut Curie (Author)
ID Ghinea, Nicolae, Institut Curie (Author)
ID De Marco, Ario, UNG (Author), et al. |
|---|
| Files: |
This document has no files that are freely available to the public. This document may have a physical copy in the library of the organization, check the status via COBISS.  |
|---|
| Language: | English |
|---|
| Work type: | Not categorized |
|---|
| Typology: | 1.01 - Original Scientific Article |
|---|
| Organization: | UNG - University of Nova Gorica
|
|---|
| Abstract: | Antibodies are essential reagents that are increasingly used in diagnostics and therapy. Their specificity
and capacity to recognize their native antigen are critical characteristics for their in vivo application.
Follicle-stimulating hormone receptor is a GPCR protein regulating ovarian follicular maturation and
spermatogenesis. Recently, its potentiality as a cancer biomarker has been demonstrated but no antibody
suitable for in vivo tumor targeting and treatment has been characterized so far. In this paper we describe
the first successful attempt to recover recombinant antibodies against the FSHR and that: i) are directly
panned from a pre-immune library using whole cells expressing the target receptor at their surface; ii)
show inhibitory activity towards the FSH-induced cAMP accumulation; iii) do not share the same epitope
with the natural binder FSH; iv) can be produced inexpensively as mono- or bivalent functional molecules
in the bacterial cytoplasm. We expect that the proposed biopanning strategy will be profitable to
identify useful functional antibodies for further members of the GPCR class. |
|---|
| Keywords: | nanobodies, GPCR proteins, FSHR, panning, pre-immune antibody library |
|---|
| Publication version: | Version of Record |
|---|
| Year of publishing: | 2017 |
|---|
| Number of pages: | 1567-1572 |
|---|
| Numbering: | 493 |
|---|
| PID: | 20.500.12556/RUNG-3322-b86c7cca-992c-0d39-70bc-b8e3cc19c7ad |
|---|
| COBISS.SI-ID: | 4933627 |
|---|
| NUK URN: | URN:SI:UNG:REP:4WYPVXVK |
|---|
| Publication date in RUNG: | 19.10.2017 |
|---|
| Views: | 4934 |
|---|
| Downloads: | 0 |
|---|
| Metadata: |    |
|---|
|
:
|
Copy citation |
|---|
| | | | Average score: | (0 votes) |
|---|
| Your score: | Voting is allowed only for logged in users. |
|---|
| Share: |  |
|---|
Hover the mouse pointer over a document title to show the abstract or click
on the title to get all document metadata. |
