The HSE (Heat Shock Response) Luciferase Reporter Lentiviruses are replication incompetent, HIV-based, VSV-G pseudotyped lentiviral particles ready to transduce most mammalian cells, including primary and non-dividing cells. These viruses transduce cells with the firefly luciferase gene driven by multiple copies of the heat shock response element (HSE) located upstream of the minimal TATA promoter. The lentiviruses also transduce a puromycin selection gene (Figure 1). After transduction, the heat shock response in the target cells can be monitored by measuring luciferase activity.
Figure 1. Schematic of the lenti-vector used to generate the HSE luciferase reporter lentivirus.
●
Product Data Gallery
Activation of HSE luciferase reporter activity in HeLa cells by 17-AAG.
The lentiviruses were produced in HEK293T cells in medium containing 90% DMEM + 10% FBS. Virus particles can be packaged in custom formulations by special request, for an additional fee.
Background
The Heat Shock Response (HSR) is crucial for cells to adapt to stressful conditions. In the presence of high temperatures, oxidative stress or heavy metals, several proteins can unfold and become unable to perform their normal functions. This in turn can result in cell damage and/or death. To maintain proteins with the proper structure the expression of Heat Shock Proteins (HSP) is induced. Expression of HSPs is regulated by the transcription factor Heat Shock Factor 1 (HSF1). When cellular stress occurs HSF1 undergoes a confirmation change and moves to the nucleus, where it can bind to Heat Shock Elements (HSE) and lead to transcription of the HSP mRNA. Dysfunction in the HSR can lead to pathologies such as neurodegenerative diseases and cancer. Targeting HSE may prove beneficial in the treatment of pathologies linked to defective HSR.
Storage/Stability
Lentiviruses are shipped with dry ice. For long-term storage, it is recommended to store the lentiviruses at -80°C for up to 12 months from date of receipt. Avoid repeated freeze/thaw cycles. Titers can drop significantly with each freeze/thaw cycle.
Growth Media
For best results, the use of validated and optimized media from BPS Bioscience is highly recommended. Other preparations or formulations of media may result in suboptimal performance.
Media Required for the Proposed Assay
Thaw Medium 1 (BPS Bioscience, #60187): MEM medium supplemented with 10% FBS, 1% non-essential amino acids, 1 mM Na pyruvate, 1% Penicillin/Streptomycin.
Applications
Expression of HSF1-dependent luciferase reporter to study the heat shock response.
To generate HSE luciferase reporter stable cells, remove the growth medium 48 hours after transduction and replace it with fresh growth medium containing the appropriate amount of puromycin, for antibiotic selection of transduced cells.
The following Lentivirus Reporter Controls are available from BPS Bioscience to meet your experimental needs:
Negative Control Luciferase Lentivirus (BPS Bioscience #79578): Ready-to-transduce lentiviral particles expressing firefly luciferase under the control of a minimal promoter. This negative control is important to establish the specificity of any treatments and to determine background reporter activity.
Renilla Luciferase Lentivirus (BPS Bioscience #79565): Ready-to-transduce lentiviral particles expressing Renilla luciferase under the CMV promoter. The Renilla luciferase lentivirus can serve as an internal control to overcome sample-to-sample variability when performing dual-luciferase reporter assays.
Firefly Luciferase Lentivirus (BPS Bioscience #79692-G, #79692-H, #79692-P): Ready-to-transduce lentiviral particles expressing firefly luciferase under the CMV promoter. It serves as a positive control for transduction optimization studies.
Biosafety The lentiviruses are produced with SIN (self-inactivation) lentivector which ensures self-inactivation of the lentiviral construct after transduction and integration into the genomic DNA of the target cells. None of the HIV genes (gag, pol, rev) will be expressed in the transduced cells, as they are expressed from packaging plasmids lacking the packing signal and are not present in the lentivirus particle. Although the pseudotyped lentiviruses are replication-incompetent, they require the use of a Biosafety Level 2 facility. BPS Bioscience recommends following all local federal, state, and institutional regulations and using all appropriate safety precautions.