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Difference between revisions of "Preparation of SUIT chemicals"

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{{MitoPedia
{{MitoPedia
|description='''Preparation of SUIT chemicals''' describes the preparation of chemicals used in Substrate-Uncoupler-Inhibitor Ttitration (SUIT) protocols.
|description='''Preparation of SUIT chemicals''' describes the preparation of chemicals used in Substrate-Uncoupler-Inhibitor Ttitration (SUIT) protocols.
|info=[[MiPNet09.12 O2k-Titrations]]
|info=[[MiPNet09.12 O2k-Titrations]], [https://wiki.oroboros.at/images/3/3c/MiPNet03.02_Chemicals-Media.pdf MiPNet03.02_Chemicals-Media.pdf]
}}
}}
''Work in progress''
<!-- ''Work in progress''-->
 
  Communicated by [[Spitzer Gudrun]] 2021-03-19
  Communicated by [[Spitzer Gudrun]] 2021-03-19
There could be a Category called "Chemical Preparations" listing all preparation instructions. Additionally there could be a page providing recommendations. This could be called Chemical preparation recommendations.
How do my ideas fit into BioBlast? Somehow close to the SUIT titration instructions or the same way as O2k-Mitochondrial Preparations?
Preparing Chemicals for SUIT Titrations
Subtitle: Tips and Tricks, General Recommendations...


== General recommendations ==
== General recommendations ==
* In General, chemicals used in SUIT protocols are added in '''kinetically saturated''' concentration. That means that small deviations from the concentrations indicated in the preparation instructions will not have any negative effect on the experiment (this was for example tested for Pyruvate, Glycerophosphate and Azide).
* The chemicals used in mitochondrial studies have to be of '''highest purity grade''' possible. Functional activity of mitochondria, whether in their natural cytosolic habitat or in experimental medium, are highly sensitive to fluctuations of the environmental ionic content.
* Most stock solutions are prepared in concentrations that allow for low titration volumina between 1 and 10 µL. As long as the solubility of a compound is high enough, stock solutions that have to be titrated in 100 µL steps should be avoided.
* Most stock solutions are prepared in concentrations that allow for low '''titration volumina''' between '''1 and 10 µL''' to avoid unnecessary dilution of the experiment.
* The standard process to prepare a stock solution is to weigh the substance, transfer it to a volumetric glass flask and '''adjust the volume''' of the solvent to a specific value. Only in some cases (e.g. when a small volume has to be prepared fresh for every experiment like Pyruvate or if the compound is very toxic like Azide or expensive like Glycerophosphate) the solvent is added instead of adjusted. For some compounds (P, Gp, Glu, Azd) the correct volume to be added was experimentally determined 2021-02.
* The pH of stock solutions should be adjusted to '''pH 7'''. However, if not easily feasible (e.g. Pyruvate has to be prepared freshly every day in a volume of only 200 µL), a deviation from pH 7 is acceptable as long as the titration volume is low and the experimental medium is bufferd.
* [[Volume determination in the lab]]
* The standard process to prepare a stock solution is to weigh the substance, transfer it to a volumetric glass flask and '''adjust the volume''' of the solvent to a specific value. Only in some cases (e.g. when a small volume has to be prepared fresh for every experiment like Pyruvate or if the compound is very toxic like Azide or expensive, the solvent is added instead of adjusted. For some compounds (P, Gp, Glu, Azd) the correct volume to be added was experimentally determined 2021-02 (see [[Volume_of_the_solute| Volume of the solute]]).
* The '''molar mass''' is very useful as an identifier for chemicals. Different abbreviations or terms are used by vendors, e.g. 'MW' (molecular weight) on vials from Sigma-Aldrich or 'FW' (formular weight). These terms are synonyms for 'molar mass'.
* Read '''SDS''' (safety data sheets) before using toxic chemicals.
* Read safety data sheets before using toxic chemicals.
* The use of appropriately diluted stock solutions is critical for concentration-dependent substrate-uncoupler-inhibitor kinetic (SUIK) titrations.
<!--* The '''molar mass''' is a very useful as an identifier for chemicals. Different abbreviations or terms are used by vendors, e.g. 'MW' (molecular weight) on vials from Sigma-Aldrich or 'FW' (formular weight). These terms are synonyms for 'molar mass'.
* Lab equipment like balances and pipettes should be checked on a regular basis.
* Lab equipment like balances and pipettes should be checked on a regular basis.
-->
== Solvents ==
* If possible, compounds are solved in [[water]] of high purity grade. For example, in Oroboros lab we use Evoqua Water TechnologiesGmbH: deionized ultra-pure water(Ultra ClearTMTP UV UF TM).
* The stock solutions of chemicals dissolved in organic solvents like ethanol and DMSO should be prepared at highest concentrations possible, since the final concentration of solvents in the chamber should be as low as possible.
* Nevertheless, the '''effects of solvent''' on mitochondrial function and experimental sensors (ion selective electrodes) have to be evaluated in chemical background tests and control experiments.
* [[Ethanol]] used as solvent is meant to be high purity grade, abbreviated as 'ethanol abs.'
* A special care should be taken with the chemicals dissolved in ethanol, as there is a problem of evaporation and subsequent increase of concentration of stock solutions.
* Disadvantage of DMSO: freezing point of +18.55 °C (65.4 °F). When using DMSO as solvent, make sure to bring the stock solution to room temperature before filling the Hamilton syringe, to avoid blocking the needle.


== Storage ==
== Storage ==
* In Oroboros-lab, all prepared aliquots are stored in the freezer at -20°C.
* Most of the chemicals are stable and stored as refrozen aliquots of stock solutions for a long-term usage. However, some chemicals are prone to easy oxidation and have to be prepared freshly for each experiment just prior to adding to the chamber; e.g. pyruvate, α-ketoglutarate, oxaloacetate. For such chemicals, recommendations are given how to prepare the small-volume solutions while attaining a precise stock concentration.
* Chemicals stored in the fridge or freezer should be allowed to reach room temperature before opening. Otherwise water will condensate quickly on every accesible surface.
* In Oroboros-lab, all aliquots that are not prepared freshly are stored in the freezer at '''-20 °C'''.
* It is advisable to divide stock solutions in small portions before freezing them at -20°C instead of storing the whole amount of stock solution in one vial. Thereby the risk of contamination or water condensation and the number of freezing-thawing-cycles is lower.
* It is advisable to divide stock solutions in small portions before freezing them at -20°C instead of storing the whole amount of stock solution in one vial. Thereby the risk of contamination or water condensation and the number of freezing-thawing-cycles is lower.
* In gerenal, transparent '''Eppendorf tubes''' are '''used to store''' aliquoted stock solutions. Exceptions:
* In gerenal, transparent '''Eppendorf tubes''' are '''used to store''' aliquoted stock solutions. Exceptions:
** light sensitive compounds are stored in dark glass or dark Eppendorf tubes.
** '''light sensitive''' compounds are stored in dark glass or dark Eppendorf tubes.
** black, non-transparent Eppis will protect compounds from light, but handling of small volumes of stock solutions is uncomfortable because it is hard to see the liquid in the Eppi.
** black, non-transparent Eppis will protect compounds from light, but handling of small volumes of stock solutions is uncomfortable because it is hard to see the liquid in the Eppi.
** if the solvent is EtOH, glass vials are used instead of Eppis, because EtOH reduces the chemical stability of Eppi material (see [https://www.eppendorf.com/product-media/doc/en/114794_Userguide/Eppendorf_Consumables_Userguide_023_Tubes_Tips_Chemical-stability-consumables.pdf Chemical stability of Eppendorf Consumables]).
** if the solvent is '''EtOH, glass''' vials are used instead of Eppis, because EtOH reduces the chemical stability of Eppi material (see [https://www.eppendorf.com/product-media/doc/en/114794_Userguide/Eppendorf_Consumables_Userguide_023_Tubes_Tips_Chemical-stability-consumables.pdf Chemical stability of Eppendorf Consumables]).
** DMSO can be stored in Eppendorf tubes. They are made of PP (polypropylene) which is compatible with DMSO according to Sigma-Aldrich's [https://www.sigmaaldrich.com/content/dam/sigma-aldrich/docs/Sigma/Product_Information_Sheet/d8779pis.pdf Product Information Sheet].
** DMSO can be stored in Eppendorf tubes. They are made of PP (polypropylene) which is compatible with DMSO according to Sigma-Aldrich's [https://www.sigmaaldrich.com/content/dam/sigma-aldrich/docs/Sigma/Product_Information_Sheet/d8779pis.pdf Product Information Sheet].


== Recommendations from Zulfiya's paper ==
== Usage ==
* The chemicals used in mitochondrial studies have to be of highest purity grade possible. Functional activity of mitochondria, whether in their natural cytosolic habitat [TK1] or in experimental medium, are highly sensitive to fluctuations of the environmental ionic content.
<!--* In General, chemicals used in SUIT protocols are added in '''kinetically saturated''' concentration. That means that small deviations from the concentrations indicated in the preparation instructions will not have any negative effect on the experiment (this was for example tested for Pyruvate, Glycerophosphate and Azide).-->
* Most of the chemicals are stable and stored as refrozen aliquots of stock solutions for a long-term usage. However, some chemicals are prone to easy oxidation and have to be prepared freshly for each experiment just prior to adding to the chamber; e.g. pyruvate α-ketoglutarate, oxaloacetate[GS2] [ZO3] [TK4] . For such chemicals, recommendations are given how to prepare the small-volume solutions while attaining a precise stock concentration.
* Solutions stored in fridge or freezer should be '''prewarmed''' to room temperature before opening to avoid air-water condensation.
* Solutions stored in fridge or freezer should be prewarmed to room temperature before opening to avoid air-water condensation; and be mixed carefully[TK5]  to avoid phase separation that may occur in cold solutions, causing compounds’ precipitation. During the experiment, the stock solutions should be kept on ice. [TK6] Some of the chemicals (e.g., ADP, NADH) are forbidden to be refrozen[TK7]  and new frozen aliquots are recommended to be used in each experiment.
* Solutions should be mixed carefully to avoid phase separation that may occur in cold solutions, causing compounds’ precipitation.
* The stock solutions of chemicals dissolved in organic solvents like ethanol and DMSO should be prepared at high concentrations possible, since the final concentration [TK8] of solvents in the chamber should be as low as possible. Nevertheless, the effects of solvent on mitochondrial function and experimental sensors (ion selective electrodes) have to be evaluated in chemical background tests and control experiments.
* During the experiment, the stock solutions should be kept on ice.
* A special care [TK9] should be taken with the chemicals dissolved in ethanol, as there is a problem of evaporation and subsequent increase of concentration of stock solutions.
* Some of the chemicals (e.g., ADP, NADH) are forbidden to be refrozen and new frozen aliquots are recommended to be used in each experiment.
* The use of appropriately diluted stock solutions is critical for concentration-dependent substrate-uncoupler-inhibitor kinetic (SUIK) titrations.
== Recommendations from ]https://wiki.oroboros.at/images/3/3c/MiPNet03.02_Chemicals-Media.pdf] ==
5.1.Solutions stored at low temperature: Mix carefully after re-warming, since phase separation may occur and compounds may precipitate in cold solutions. During the course of the experiment, keep stock solutions on ice.
5.2.Solutions containing ethanol:there may be a problem of evaporation and subsequent increase of concentration of stock solutions.
5.3.Chemicals dissolved in ethanol or DMSO: To check the influence of ethanol or DMSO on mitochondrial function and experimental sensors (ion selective electrodes), the same additions of pure solvents should be used in carrier control experiments.
5.4.For all stock solutions of mitochondrial substrates, inhibitors, and uncouplers;the total volumes of solutions are indicated.
5.5.Store chemicals as indicated by the suppliers. The storage of prepared solutions areindicated in the comments.
5.6.Aliquots of stocks for rotenone, succinate, glutamate, malate, and oligomycin can be refrozen for later use, since these chemicals are stable.


== Disposal ==
== Disposal ==
* Some of the chemicals used have severe toxic effects on the environment. Make sure to dispose the correctly.
* Some of the chemicals used have severe toxic effects on the environment. Make sure to dispose them correctly.


{{MitoPedia concepts
{{MitoPedia concepts

Latest revision as of 08:50, 17 June 2021


high-resolution terminology - matching measurements at high-resolution


Preparation of SUIT chemicals

Description

Preparation of SUIT chemicals describes the preparation of chemicals used in Substrate-Uncoupler-Inhibitor Ttitration (SUIT) protocols.


Reference: MiPNet09.12 O2k-Titrations, MiPNet03.02_Chemicals-Media.pdf

Communicated by Spitzer Gudrun 2021-03-19

General recommendations

  • The chemicals used in mitochondrial studies have to be of highest purity grade possible. Functional activity of mitochondria, whether in their natural cytosolic habitat or in experimental medium, are highly sensitive to fluctuations of the environmental ionic content.
  • Most stock solutions are prepared in concentrations that allow for low titration volumina between 1 and 10 µL to avoid unnecessary dilution of the experiment.
  • The pH of stock solutions should be adjusted to pH 7. However, if not easily feasible (e.g. Pyruvate has to be prepared freshly every day in a volume of only 200 µL), a deviation from pH 7 is acceptable as long as the titration volume is low and the experimental medium is bufferd.
  • The standard process to prepare a stock solution is to weigh the substance, transfer it to a volumetric glass flask and adjust the volume of the solvent to a specific value. Only in some cases (e.g. when a small volume has to be prepared fresh for every experiment like Pyruvate or if the compound is very toxic like Azide or expensive, the solvent is added instead of adjusted. For some compounds (P, Gp, Glu, Azd) the correct volume to be added was experimentally determined 2021-02 (see Volume of the solute).
  • Read SDS (safety data sheets) before using toxic chemicals.
  • The use of appropriately diluted stock solutions is critical for concentration-dependent substrate-uncoupler-inhibitor kinetic (SUIK) titrations.

Solvents

  • If possible, compounds are solved in water of high purity grade. For example, in Oroboros lab we use Evoqua Water TechnologiesGmbH: deionized ultra-pure water(Ultra ClearTMTP UV UF TM).
  • The stock solutions of chemicals dissolved in organic solvents like ethanol and DMSO should be prepared at highest concentrations possible, since the final concentration of solvents in the chamber should be as low as possible.
  • Nevertheless, the effects of solvent on mitochondrial function and experimental sensors (ion selective electrodes) have to be evaluated in chemical background tests and control experiments.
  • Ethanol used as solvent is meant to be high purity grade, abbreviated as 'ethanol abs.'
  • A special care should be taken with the chemicals dissolved in ethanol, as there is a problem of evaporation and subsequent increase of concentration of stock solutions.
  • Disadvantage of DMSO: freezing point of +18.55 °C (65.4 °F). When using DMSO as solvent, make sure to bring the stock solution to room temperature before filling the Hamilton syringe, to avoid blocking the needle.

Storage

  • Most of the chemicals are stable and stored as refrozen aliquots of stock solutions for a long-term usage. However, some chemicals are prone to easy oxidation and have to be prepared freshly for each experiment just prior to adding to the chamber; e.g. pyruvate, α-ketoglutarate, oxaloacetate. For such chemicals, recommendations are given how to prepare the small-volume solutions while attaining a precise stock concentration.
  • In Oroboros-lab, all aliquots that are not prepared freshly are stored in the freezer at -20 °C.
  • It is advisable to divide stock solutions in small portions before freezing them at -20°C instead of storing the whole amount of stock solution in one vial. Thereby the risk of contamination or water condensation and the number of freezing-thawing-cycles is lower.
  • In gerenal, transparent Eppendorf tubes are used to store aliquoted stock solutions. Exceptions:
    • light sensitive compounds are stored in dark glass or dark Eppendorf tubes.
    • black, non-transparent Eppis will protect compounds from light, but handling of small volumes of stock solutions is uncomfortable because it is hard to see the liquid in the Eppi.
    • if the solvent is EtOH, glass vials are used instead of Eppis, because EtOH reduces the chemical stability of Eppi material (see Chemical stability of Eppendorf Consumables).
    • DMSO can be stored in Eppendorf tubes. They are made of PP (polypropylene) which is compatible with DMSO according to Sigma-Aldrich's Product Information Sheet.

Usage

  • Solutions stored in fridge or freezer should be prewarmed to room temperature before opening to avoid air-water condensation.
  • Solutions should be mixed carefully to avoid phase separation that may occur in cold solutions, causing compounds’ precipitation.
  • During the experiment, the stock solutions should be kept on ice.
  • Some of the chemicals (e.g., ADP, NADH) are forbidden to be refrozen and new frozen aliquots are recommended to be used in each experiment.

Disposal

  • Some of the chemicals used have severe toxic effects on the environment. Make sure to dispose them correctly.


MitoPedia concepts: SUIT concept 


MitoPedia topics: Inhibitor, Substrate and metabolite, Uncoupler, Permeabilization agent