Toolkit/lucigenin luminescence assay

lucigenin luminescence assay

Assay Method·Research·Since 1997

Also known as: lucigenin, lucigenin luminescence

Taxonomy: Technique Branch / Method. Workflows sit above the mechanism and technique branches rather than replacing them.

Summary

An example is the luminescence that can be elicited from lucigenin... the use of lucigenin as a “specific” detector of O·̄2 continues... lucigenin was shown to function, much as does paraquat, to increase intracellular O·̄2 production.

Usefulness & Problems

Why this is useful

Lucigenin luminescence is used as a luminescent detector in superoxide studies. The review emphasizes that its chemistry requires prior reduction and can itself lead to superoxide generation.; luminescent detection of superoxide-related chemistry

Source:

Lucigenin luminescence is used as a luminescent detector in superoxide studies. The review emphasizes that its chemistry requires prior reduction and can itself lead to superoxide generation.

Source:

luminescent detection of superoxide-related chemistry

Problem solved

It aims to provide a convenient luminescent measure of superoxide-related activity.; attempts to provide a luminescent readout for superoxide

Source:

It aims to provide a convenient luminescent measure of superoxide-related activity.

Source:

attempts to provide a luminescent readout for superoxide

Problem links

attempts to provide a luminescent readout for superoxide

Literature

It aims to provide a convenient luminescent measure of superoxide-related activity.

Source:

It aims to provide a convenient luminescent measure of superoxide-related activity.

Taxonomy & Function

Primary hierarchy

Technique Branch

Method: A concrete measurement method used to characterize an engineered system.

Target processes

recombination

Implementation Constraints

cofactor dependency: cofactor requirement unknownencoding mode: genetically encodedimplementation constraint: context specific validationoperating role: sensor

The assay requires lucigenin and a luminescence readout system, but the review stresses that the reagent's own redox chemistry is a major confounder.; not suitable as a specific intracellular superoxide detector based on the review's critique

It does not provide a specific measure of intracellular superoxide because lucigenin can itself produce superoxide and perturb the system being measured.; misused as a specific detector of superoxide; lucigenin can generate superoxide through autoxidation of its monocation radical; can increase intracellular superoxide production

Validation

Cell-freeBacteriaMammalianMouseHumanTherapeuticIndep. Replication

Supporting Sources

Ranked Claims

Claim 1review summarysupports1997Source 1needs review

Detector molecules such as ferricytochrome c and spin-trapping agents are used to detect superoxide, but they are not specific for superoxide and often rely on SOD inhibition to lend specificity.

Claim 2review summarysupports1997Source 1needs review

Lucigenin luminescence is an inappropriate specific detector of superoxide because lucigenin chemistry can itself generate superoxide and increase intracellular superoxide production.

Claim 3review summarysupports1997Source 1needs review

Luminol luminescence is misused as a superoxide measurement because the luminol radical can generate superoxide and the signal can be caused by multiple oxidants.

Claim 4review summarysupports1997Source 1needs review

Nitroblue tetrazolium is an artifactual superoxide detector because tetrazolium radical intermediates can generate superoxide, making SOD-inhibitable signal possible even when superoxide was not initially present.

Claim 5review summarysupports1997Source 1needs review

Rapid inactivation of [4Fe-4S]-containing dehydratases such as aconitase can be used as a reliable measure of intracellular superoxide, although other oxidants such as peroxynitrite can also inactivate aconitase.

Approval Evidence

1 source1 linked approval claimfirst-pass slug lucigenin-luminescence-assay
An example is the luminescence that can be elicited from lucigenin... the use of lucigenin as a “specific” detector of O·̄2 continues... lucigenin was shown to function, much as does paraquat, to increase intracellular O·̄2 production.

Source:

review summarysupports

Lucigenin luminescence is an inappropriate specific detector of superoxide because lucigenin chemistry can itself generate superoxide and increase intracellular superoxide production.

Source:

Comparisons

Source-stated alternatives

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Source:

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Source-backed strengths

produces a luminescent signal linked to superoxide-related chemistry

Source:

produces a luminescent signal linked to superoxide-related chemistry

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Shared frame: source-stated alternative in extracted literature

Strengths here: produces a luminescent signal linked to superoxide-related chemistry.

Relative tradeoffs: misused as a specific detector of superoxide; lucigenin can generate superoxide through autoxidation of its monocation radical; can increase intracellular superoxide production.

Source:

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Shared frame: source-stated alternative in extracted literature

Strengths here: produces a luminescent signal linked to superoxide-related chemistry.

Relative tradeoffs: misused as a specific detector of superoxide; lucigenin can generate superoxide through autoxidation of its monocation radical; can increase intracellular superoxide production.

Source:

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Shared frame: source-stated alternative in extracted literature

Strengths here: produces a luminescent signal linked to superoxide-related chemistry.

Relative tradeoffs: misused as a specific detector of superoxide; lucigenin can generate superoxide through autoxidation of its monocation radical; can increase intracellular superoxide production.

Source:

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Shared frame: source-stated alternative in extracted literature

Strengths here: produces a luminescent signal linked to superoxide-related chemistry.

Relative tradeoffs: misused as a specific detector of superoxide; lucigenin can generate superoxide through autoxidation of its monocation radical; can increase intracellular superoxide production.

Source:

The review contrasts lucigenin with luminol, nitroblue tetrazolium, ferricytochrome c, spin-trapping agents, and aconitase-based measurement.

Ranked Citations

  1. 1.
    StructuralSource 1Journal of Biological Chemistry1997Claim 1Claim 2Claim 3

    Seeded from load plan for claim c2. Extracted from this source document.