Recombinant HTLV-1 Envelope Protein, sFc-tagged
Specification
Related Products
| Cat#: |
HTL-288 |
| Product Name: |
Recombinant HTLV-1 Envelope Protein, sFc-tagged |
| Description: |
Recombinant human T-cell lymphotropic virus type 1 (HTLV-1) envelope protein. The protein was produced in HEK293 cells and purified from culture supernatant with a TEV cleavage site and C-terminal sheep Fc-tag. |
| Gene: |
Envelope |
| Species: |
HTLV-1 |
| Source: |
HEK293 |
| Synonyms: |
HTLV-1 Envelope |
| Notes: |
This product is intended for research and manufacturing uses only. It is not a diagnostic device. The user assumes all responsibility for care, custody and control of the material, including its disposal, in accordance with all regulations. |
| Tags: |
C-terminal sheep Fc |
| Background: |
HTLV-1 and HTLV-2 require cell-to-cell contact for efficient transmission and utilize envelope glycoprotein-mediated cell binding and entry (envelope glycoprotein gp62). Specific enzymatic cleavages in vivo yield mature proteins. Envelope glycoproteins are synthesized as an inactive precursor that is N-glycosylated and processed likely by host cell furin or by a furin-like protease in the Golgi to yield the mature SU (gp46) and TM (gp21) proteins. The cleavage site between SU and TM requires the minimal sequence [KR]-X-[KR]-R. HTLV-1 attachment and fusion to target cells begins when surface subunit (SU) of the HTLV-1 envelope glycoprotein interacts with three cellular surface receptors: Glucose Transporter (GLUT1), Heparin Sulfate Proteoglycan (HSPG) and the VEGF-165 receptor Neuropilin-1 (NRP-1). These receptors are widely distributed on target cells. The HTLV-1 and HTLV-2 surface (SU) and transmembrane (TM) subunits of Env share 65% and 79% residue identity, respectively. Despite this high similarity, HTLV-1 and HTLV-2 utilize a slightly different complex of receptor molecules. HTLV-1 utilizes heparan sulfate proteoglycan (HSPG) and neuropilin-1 (NRP1) for binding and glucose transporter 1 (GLUT1) for entry. HTLV-2 also utilizes NRP1 and GLUT1, but not HSPGs (Eusebio-Ponce et al., 2019; Martinez et al., 2019). The surface protein (SU) attaches the virus to the host cell by binding to its receptor. This interaction triggers the refolding of the transmembrane protein (TM) and is thought to activate its fusogenic potential by unmasking its fusion peptide. Fusion occurs at the host cell plasma membrane and the transmembrane protein (TM) acts as a class I viral fusion protein. Membrane fusion leads to delivery of the nucleocapsid into the cytoplasm. |
For research use only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
