Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Difference between revisions of "Atractyloside"

From Bioblast
(replaced FW by M and added units g*mol-1)
 
(One intermediate revision by one other user not shown)
Line 7: Line 7:
{{MitoPedia methods|type=Inhibitor PS
{{MitoPedia methods|type=Inhibitor PS
}}
}}
{{MitoPedia topics
__TOC__
|mitopedia topic=Inhibitor
|type=Inhibitor PS
}}
== Application in [[HRR]] ==
== Application in [[HRR]] ==


::: '''Atr: Atractyloside'''  (Atractyloside dipotassium salt,  C<sub>30</sub>H<sub>44</sub>O<sub>16</sub>S<sub>2</sub>K<sub>2</sub>); Sigma A 6882,  250 mg, store at R.T.; FW = 802.99 containing 2.5 mol H<sub>2</sub>O/mol.
::: '''Atr: Atractyloside'''  (Atractyloside dipotassium salt,  C<sub>30</sub>H<sub>44</sub>O<sub>16</sub>S<sub>2</sub>K<sub>2</sub>); Sigma A 6882,  250 mg, store at R.T.; M = 802.99 g·mol<sup>-1</sup> containing 2.5 mol H<sub>2</sub>O/mol.


:::: <span style="color:#8B008B"> '''Caution:''' very toxic.</span>
:::: <span style="color:#8B008B"> '''Caution:''' very toxic.</span>




::: '''Preparation of 50 mM stock solution''' (dissolved in H<sub>2</sub>0):  
:::: '''Preparation of 50 mM stock solution''' (dissolved in H<sub>2</sub>0):  


::::# Weigh 40.2 mg atractyloside.
::::# Weigh 40.2 mg atractyloside.
Line 27: Line 24:




::: '''O2k manual titrations'''  [[MiPNet09.12 O2k-Titrations]]
:::» '''O2k manual titrations'''  [[MiPNet09.12 O2k-Titrations]]


::::* Titration volume: 30 µl using a 50 µl syringe (2 ml O2k-chamber).
::::* Titration volume: 30 µl using a 50 µl syringe (2 ml O2k-chamber).
::::* Final concentration: 0.75 mM.
::::* Final concentration: 0.75 mM.
::::* '''Comment:''' With Atr, a very high concentration is required for full   inhibition. [[carboxyatractyloside|Carboxyatractyloside]] (Cat) is considered to be much more specific than Atr, and the effective concentration required is much much lower.
::::* '''Comment:''' With Atr, a very high concentration is required for full inhibition. [[carboxyatractyloside|Carboxyatractyloside]] (Cat) is considered to be much more specific than Atr, and the effective concentration required is much much lower.
{{MitoPedia topics
|mitopedia topic=Inhibitor
|type=Inhibitor PS
}}

Latest revision as of 12:47, 12 February 2021


high-resolution terminology - matching measurements at high-resolution


Atractyloside

Description

Atractyloside is an inhibitor of the adenine nucleotide translocator (ANT). It is an extremely toxic glycoside that inhibits oxidative phosphorylation by blocking the transfer of adenosine nucleotides through the mitochondrial membrane.

Abbreviation: Atr

Reference: MiPNet03.02; MiPNet09.12



Application in HRR

Atr: Atractyloside (Atractyloside dipotassium salt, C30H44O16S2K2); Sigma A 6882, 250 mg, store at R.T.; M = 802.99 g·mol-1 containing 2.5 mol H2O/mol.
Caution: very toxic.


Preparation of 50 mM stock solution (dissolved in H20):
  1. Weigh 40.2 mg atractyloside.
  2. Dissolve in 1 ml H2O (it dissolves better in warm water).
  3. Divide into 0.2 ml aliquots.
  4. Store at -20 °C.


» O2k manual titrations MiPNet09.12 O2k-Titrations
  • Titration volume: 30 µl using a 50 µl syringe (2 ml O2k-chamber).
  • Final concentration: 0.75 mM.
  • Comment: With Atr, a very high concentration is required for full inhibition. Carboxyatractyloside (Cat) is considered to be much more specific than Atr, and the effective concentration required is much much lower.

MitoPedia topics: Inhibitor