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Next stop: The industry's top trade shows
Agarose Bead Technologies (ABT) is excited to announce our participation in several important trade fairs this October.
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Agarose Bead Technologies expands facility to meet rising global demand for novel therapies market
Agarose Bead Technologies has enhanced its Burgos facility by boosting its agarose resin production to 100,000 liters annually to position itself as a powerhouse in the novel therapies market.
Read moreSee you at Bioprocess International Conference and Exhibition 2024
ABT will be exhibiting at one of the most prestigious events in the bioprocessing industry, the Bioprocess International Conference. This prestigious event will be held...
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Unveiling the role of TAOK3 and SHP-1 in T cell activation: Protein isolation and purification
Modulation of SHP-1 abundance by TAOK3 serves as a rheostat for TCR signaling and determines the activation threshold of T lymphocytes.
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"Modulation of SHP-1 abundance by TAOK3 serves as a rheostat for TCR signaling and determines the activation threshold of T lymphocytes"
Significant effort has been invested in identifying pathways that regulate the activation of T cells.
Among these pathways, the Salvador-Warts-Hippo (SWH) pathway stands out for its role in regulating cell proliferation and apoptosis, as well as its involvement in numerous functions of T cells, such as the formation of the immunological synapse and the memory of T lymphocytes. This pathway involves several families of protein kinases.
Beyond the core enzymes of this pathway, this article focuses on the thousand-and-one amino acid kinases (TAOKs) and SHP-1 (Figure 1). Modulation of SHP-1 abundance by TAOK3 thus serves as a rheostat for T cell receptor (TCR) signaling and determines the activation threshold of T lymphocytes.
The results of the study presented in this article indicate that thousand-and-one-amino-acid kinase 3 (TAOK3) is a serine and threonine kinase that is essential for TCR signaling. Its absence results in reduced TCR signaling and increased interaction of the tyrosine phosphatase SHP-1 with the kinase LCK, a key downstream mediator of TCR signaling (Figure 1B).
Figure 1. A) SHP-1–TAOK3 interaction model structures and experimentally defined interaction sites. B) Model for TAOK3-mediated SHP-1 degradation and regulation of TCR signaling.
To reach this conclusion, the scientific team of this study conducted precise molecular and biochemical analyses. Prior to these steps, it is crucial to isolate the enzyme of study in an optimal way in order to obtain the most reliable results.
The team of scientists uses the standard 4% B Agarose Beads (50-150 μm) from Agarose Bead Technologies, which facilitates the purification and separation of the proteins of interest.
This agarose resin from ABT is used in the IP procedure to isolate specific proteins related to T-cell receptor signaling and TAOK3 function in T cells.
It is of the utmost importance to select an appropriate methodology in order to achieve the highest possible purity, which is essential for the conduct of scientifically valid studies.
The effectiveness, specificity, and selectivity of ABT's agarose resins play a significant role in the reproducibility and reliability of results obtained in experiments that require protein purification and separation steps.
- Poirier A, Ormonde JVS, Aubry I, Abidin BM, Feng CH, Martinez-Cordova Z, Hincapie AM, Wu C, Pérez-Quintero LA, Wang CL, Gingras AC, Madrenas J, Tremblay ML. The induction of SHP-1 degradation by TAOK3 ensures the responsiveness of T cells to TCR stimulation.Sci Signal. 2024 Jan 2;17(817):eadg4422. doi: 10.1126/scisignal.adg4422. Epub 2024 Jan 2. PMID: 38166031.
- Figure 1A. SHP-1–TAOK3 interaction model based on AlphaFold structures and experimentally defined interaction sites. (Fig. 6. From The induction of SHP-1 degradation by TAOK3 ensures the responsiveness of T cells to TCR stimulation)
- Figure 1B. Model for TAOK3-mediated SHP-1 degradation and regulation of TCR signaling. (Fig. 7. From The induction of SHP-1 degradation by TAOK3 ensures the responsiveness of T cells to TCR stimulation)