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XB-ART-55927
PLoS One January 1, 2019; 14 (5): e0216083.

Isolation of nanobodies against Xenopus embryonic antigens using immune and non-immune phage display libraries.

Itoh K , Reis AH , Hayhurst A , Sokol SY .


Abstract
The use of Xenopus laevis as a model for vertebrate developmental biology is limited by a lack of antibodies specific for embryonic antigens. This study evaluated the use of immune and non-immune phage display libraries for the isolation of single domain antibodies, or nanobodies, with specificities for Xenopus embryonic antigens. The immune nanobody library was derived from peripheral blood lymphocyte RNA obtained from a llama immunized with Xenopus gastrula homogenates. Screening this library by immunostaining of embryonic tissues with pooled periplasmic material and sib-selection led to the isolation of several monoclonal phages reactive with the cytoplasm and nuclei of gastrula cells. One antigen recognized by a group of nanobodies was identified using a reverse proteomics approach as nucleoplasmin, an abundant histone chaperone. As an alternative strategy, a semi-synthetic non-immune llama nanobody phage display library was panned on highly purified Xenopus proteins. This proof-of-principle approach isolated monoclonal nanobodies that specifically bind Nuclear distribution element-like 1 (Ndel1) in multiple immunoassays. Our results suggest that immune and non-immune phage display screens on crude and purified embryonic antigens can efficiently identify nanobodies useful to the Xenopus developmental biology community.

PubMed ID: 31048885
PMC ID: PMC6497274
Article link: PLoS One
Grant support: [+]
Genes referenced: mbp ndel1 npm1 npm2 pafah1b1


Article Images: [+] show captions
References [+] :
Asashima, Mesodermal induction in early amphibian embryos by activin A (erythroid differentiation factor). 2019, Pubmed, Xenbase


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