South Bay Bio - Bioassays, Enzymes & Advanced TR-FRET Technology - Distributed in the UK & Ireland by Caltag Medsystems
South Bay Bio
South Bay Bio, LLC, formed in 2016, are a platform technology company that provides expertise in the ubiquitin proteasome system (UPS) and other innovative research areas, like UPS related assay development, HTS, protein purification, bioconjugation and custom biochemistry services.
The collaboration between South Bay Bio and AdipoGen Life Sciences allows us to bring the South Bay Bio product range to our UK & Ireland customers.
See the Products Available:
Sensitive E3 Ligase TR-FRET Assays
South Bay Bio's homogeneous Real-Time TR-FRET ubiquitin conjugation assays are simple; the format is 96 or 384-well low-volume plates (making them well suited for HTS). Using ubiquitin either labelled with Europium-Cryptate (donor) or Cyanine 5 (acceptor), for the first time, ubiquitin conjugation and deconjugation can be measured homogenously in Real-Time (facilitating enzyme kinetics or endpoint if preferred), with assays commonly exhibiting Z’ 0.8 and a Signal to Noise of commonly >3000%.
Auto-ubiquitination kinetics of several human recombinant E3 ligases of significant interest, namely MDM2, MuRF1, ITCH and Parkin, along with ubiquitin conjugation on substrates such as p53 and s5a have been validated, as well as TR-FRET based deconjugation kinetics of several auto-ubiquitinated ligases using USP2cd and USP7. Coupled with the assays’ short development time (as no antibody development is required for assay optimisation), the assay platform is ideally suited for a wide variety of academic and industry screening applications.
Labelled Ubiquitins for TR-FRET Experiments
Ubiquitin (Ub) is a highly conserved protein (from yeast to mammals) that plays a major role in the ubiquitination pathway. Ubiquitination, the conjugation of ubiquitin to other proteins, is essential for many cellular processes primarily linked to protein degradation. The ubiquitination process involves three steps with specific groups of enzymes in an ATP-dependent manner, which are activation with ubiquitin-activating enzymes (E1s), conjugation with ubiquitin-conjugating enzymes (E2s) and ligation with ubiquitin ligases (E3s).
Good FRET pairs exhibit no overlapping spectrum between donor and acceptor, high quantum yields and red-shifted emission (e.g. Cy5) to minimise compound interference. The best donors are cryptates, comprised of rare-earth complexes (europium or terbium) with a lanthanide embedded in a macrocycle. They exhibit long-lived fluorescence, stability and robustness necessary to survive different assay conditions. Europium Cryptate-labelled Ubiquitin is ideal for measuring Ub-chain conjugation or deconjugation as a TR-FRET donor. It's ideal protein-based TR-FRET pair acceptor is Cy5-labelled Ubiquitin.
Rhodamine-Labelled UB/UBL Derivatives – Protein Substrates
South Bay Bio offers a growing list of Rhodamine 110-labelled protein substrates for Ubiquitin Research. These protein-based substrates have a typical working concentration range of 50-500nM. Hydrolysis of the conjugate results in fluorescence observable by excitation at 485nm and emission at 535nm.
Active 20S Proteasome & 20S Immunoproteasome Proteins
The ubiquitin-proteasome pathway is the major proteolytic system in eukaryotic cells, where it catalyses the selective degradation of short-lived regulatory proteins or the rapid turnover of misfolded proteins. One of the most important proteases in this pathway is the 26S proteasome, an ATP-dependent proteolytic complex, which is formed by the association of the barrel-shaped 20S proteasome (700kDa) and two 19S (700kDa) regulatory complexes. The 20S catalytic core is composed of 4 rings of 28 non-identical subunits; 2 rings are composed of 7 a-subunits and 2 rings are composed of 7 b-subunits. The 20S catalytic core is able to degrade a variety of peptide substrates and poly-ubiquitinated proteins involved in apoptosis, DNA repair, endocytosis and cell cycle control.
The immunoproteasome is structurally similar to the constitutive 26S proteasome. The 20S core of immunoproteasome contains two outer rings composed of a-subunits and two internal 7-subunit containing rings, each possessing 3 specific subunits responsible for proteasome catalytic activity. In the 20S immunoproteasome these subunits (b1, b2, b5) are replaced by three inducible subunits: PSMB9/LMP2, PSMB10/MECL1 and PSMB8/LMP7 (b1i, b2i, b5i). These stress-induced subunits allow for the production of MHC-1 associating peptides, which are displayed as antigens on the cell surface. These displayed peptides can then be recognised by immune surveillance CD8 T cells. The 20S immunoproteasome is recognised as a strong drug target for autoimmune disease and cancer. The 20S immunoproteasome is commonly associated with the 19S, PA28 a/b or the PA28g regulatory complexes.
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