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Topic: Help with Michael acceptors and sulfhydryl groups  (Read 2744 times)

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Offline jrev005

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Help with Michael acceptors and sulfhydryl groups
« on: May 01, 2014, 06:42:36 PM »
Hi all,

I have done surface staining studies of a transport protein, using an antibody which binds an extracellular epitope.
Binding of this antibody is dependent on an S-S bridge between two cysteines to be intact. If this is disrupted the conformation of
the epitope is changed and it stops binding. I have found that the compound, curcumin, and a monocarbonyl analogue with an a,b-unsaturated carbonyl group
could decrease cell surface immunostaining using the mentioned antibody. I would normally interpret this as a downregulation of the transporter at the cell surface
caused by curcumin and my test compound. However, I have read somewhere that curcumin and a,b-unsaturated carbonyl groups can act as michael acceptors and react with sulfhydryl groups. Is there a chance that my tested compounds do not infact downregulate the surface expression of the transporter and merely disrupt the binding of antibody to the transport protein by interfering with the S-S bridge? Possibly covalently binding and modifying it?


Thanks from a non-chemist,


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Offline Babcock_Hall

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Re: Help with Michael acceptors and sulfhydryl groups
« Reply #1 on: May 01, 2014, 06:53:41 PM »
I am a little bit confused.  Sulfhydryl groups can be nucleophiles in Michael additions.  However, disulfides, which are more oxidized, are not very nucleophilic at all.  If one of your proteins has a sulfhydryl group elsewhere, I would not be surprised to see a reaction.  I don't know how quickly the reaction would occur, however.

Offline discodermolide

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Re: Help with Michael acceptors and sulfhydryl groups
« Reply #2 on: May 01, 2014, 07:19:49 PM »
What is the staining method you used?
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Offline jrev005

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Re: Help with Michael acceptors and sulfhydryl groups
« Reply #3 on: May 01, 2014, 07:31:44 PM »
^^Immunostain with a biotin conjugated monoclonal antibody targeted to an extracellular epitope. Detection with streptavidin tagged with the fluorescent molecule, phycoeryhthrin, and fluorescence was measured using a flow cytometer.

Im guessing, since Babcock_Hall mentioned that the two cysteine residues form an oxidised S-S bridge and hence are not very nucleophilic, then I shouldnt worry about my a,b-unsaturated carbonyl-containing test compounds causing a michael addition with these disulfide group. cells were only incubated for 2h at room temp.

Offline Babcock_Hall

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Re: Help with Michael acceptors and sulfhydryl groups
« Reply #4 on: May 02, 2014, 09:04:43 AM »
Do your proteins have other cysteine residues that are or might be reduced?

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