Your basket is currently empty!

ProImmune is spotlighting the capabilities of its next-generation recombinant binding reagent, Ankyron® clone CJ30451, in a recent visualization of LYVE1, a key lymphatic vessel marker.
Using fluorescence microscopy, LYVE1 was detected in cyan at the overlapping flaps of endothelial cell junctions in skin tissue. The breakthrough lies in the ultra-compact size of Ankyrons—approximately one-tenth the size of traditional monoclonal antibodies (~15 kDa)—which allows them to navigate and label tight cellular junctions with high precision. This enables detailed mapping of endothelial structures previously difficult to access.
LYVE1, beyond its structural role, serves as a crucial gatekeeper for immune surveillance and cancer metastasis, binding to hyaluronan on immune and tumor cells to facilitate their entry into the lymphatic system.
The image was captured using ProImmune’s trusted DiscoverEcho microscope platform, underscoring the synergy between advanced imaging and molecular targeting tools.
Importantly, Ankyrons are 100% animal-free, offering a sustainable and ethical alternative for researchers in immunology, oncology, and vascular biology.
Learn more about Ankyrons here.
A strategic partnership between The Pirbright Institute and ProImmune aims to develop target-binding reagents that significantly accelerate research in animal health.
Ankyrons™ are small, recombinant, target binding ankyrin repeat proteins developed by ProImmune. They are directly selected in vitro from a trillion-clone library in ribosome display and, like antibodies, can bind with high affinity to almost any target.
Due to their superior properties compared to antibodies, Ankyrons™ open new avenues for scientists to study cell behaviour, offering an alternative to traditional research antibodies. The high specificity, sensitivity and reproducibility of Ankyrons™ means they can be broadly applied in biomedical science and can be targeted against all structural proteins as a cost-effective alternative to generating custom antibodies.
In this collaboration, ProImmune is aiming to establish new Ankyrons™ for a range of crucial veterinary research applications where antibodies were previously unavailable. ProImmune has already generated and provided new Ankyrons™ to Pirbright for further study and validation, including for a broad range of bovine, porcine, avian and mosquito protein targets, as well as targets for significant animal diseases including Foot and Mouth Disease and African Swine Fever – all areas that have been underserved by traditional antibody technology.
Pirbright’s Director of Research, Professor John Hammond, said: “The collaboration brings mutual benefits to address global animal health challenges. Multiple research groups across the Institute have worked with ProImmune to develop novel Ankyrons™ that address targets from across the tree of life including mammals, insects and viral proteins.”
Dr Linda Tan, Chief Scientific Officer, ProImmune, said: “Ankyron™ technology gives researchers a better handle on biology. In this collaboration we have already demonstrated that novel Ankyrons™ can be provided rapidly to dozens of targets in areas totally unaddressed by existing research tools. We believe that over time Ankyron™ technology will have a profound impact in the wider study of biology across species and the results from this collaboration are already testament to this.”
ProImmune and the Pirbright Institute hope to make significant strides in addressing global health challenges through the development of this cutting-edge research technology that will be available to researchers world-wide, studying animal physiology and disease.
used by team at GSK to study mRNA vaccines that can protect against several Flu strains
Magini D. et al., PLOS One (2017)
Self-Amplifying
mRNA Vaccines Expressing Multiple Conserved Influenza Antigens
Confer Protection against Homologous and Heterosubtypic Viral
Challenge
http://dx.doi.org/10.1371/journal.pone.0161193
Figure:
NP-specific
CD8+ T-cell responses in lungs after influenza
challenge. BALB/c mice
were immunized i.m. twice, 8 weeks apart, with PBS, 0.1 μg of
self-amplifying mRNA (SAM®) vectors SAM(NP), SAM(M1),
SAM(M1-NP), or with 0.2 μg of SAM(NP)+SAM(M1). Four weeks after
the second immunization, mice were infected with PR8 virus.
NP-specific CD8 T cells recruited in the lungs after the
infection were characterized by flow cytometry. (a) Numbers of
NP-specific CD8+ T cells determined using
Pro5® MHC Pentamers. Data are from individual mice (depicted as dots), while solid lanes
indicate the mean±SD. (b) Cumulative frequency of Ag-specific,
cytokine-secreting CD8+ T cells, indicated as
absolute number per lung. The color code represents the
different combinations of cytokine produced by the respective
cells after in vitro stimulation with medium (m), NP147-155
peptide (NP), or M1 peptide pool (M1), as indicated. (c)
Absolute number of NP-specific CD8+ T cells positive
(black bar) or not (grey bar) for CD107a. Data derived from two
independent and merged experiments. Statistical analyses were
performed using the Mann-Whitney U test. *p<0.05; **p<0.01
compared to the PBS-treated group.
http://dx.doi.org/10.1371/journal.pone.0161193.g006
Abbreviated abstract:
Current hemagglutinin (HA)-based seasonal influenza vaccines induce
vaccine strain-specific neutralizing antibodies that usually fail to
protect against mismatched circulating viruses. Inclusion of
conserved proteins such as the nucleoprotein (NP) and the matrix
protein 1 (M1) can increase effectiveness by eliciting
cross-reactive T-cells. However, efficient priming of T-cell
responses requires the right delivery system. Here we show novel
self-amplifying mRNA (SAM®) vectors expressing influenza
NP (SAM(NP)), M1 (SAM(M1)), and NP and M1 (SAM(M1-NP)) delivered
with lipid nanoparticles (LNP) induce robust polyfunctional CD4 T
helper 1 cells, while NP-containing SAM also induced cytotoxic CD8 T
cells. Robust expansions of central memory (TCM) and
effector memory (TEM) CD4 and CD8 T cells were also
measured. An enhanced recruitment of NP-specific cytotoxic CD8
T cells was observed in the lungs of SAM(NP)-immunized mice after
influenza infection that paralleled with reduced lung viral titers
and pathology, and increased survival after homologous and
heterosubtypic influenza challenge. We show for the first time that
the co-administration of RNA (SAM(M1-NP)) and protein (monovalent
inactivated influenza vaccine (MIIV)) was feasible, induced
simultaneously NP-, M1- and HA-specific T cells and HA-specific
neutralizing antibodies, and enhanced MIIV efficacy against a
heterologous challenge.
Pro5® MHC Pentamer
Pro5® MHC Class I Pentamers are the market leading product for detecting antigen-specific T cells, you can count on consistent performance backed up by unrivalled customer service.
To ensure uniformity and consistency, each Pentamer is purified four times before being subjected to rigorous quality control acceptance testing.