Jump to content

Diazirine: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous edit
Content deleted Content added
VisualWikitext
Citation bot (talk | contribs)
Bots
5,317,880 edits
Altered pages. Add: doi-access, pmid, authors 1-1. Removed URL that duplicated identifier. Removed parameters. Some additions/deletions were parameter name changes. | Use this bot. Report bugs. | Suggested by Headbomb | Linked from Wikipedia:WikiProject_Academic_Journals/Journals_cited_by_Wikipedia/Sandbox | #UCB_webform_linked 29/122
 
(6 intermediate revisions by 5 users not shown)
Line 59: Line 59:
The substituents on the diazirine affect which carbene species is generated upon irradiation and subsequent photolytic cleavage. Diazirine substituents that are electron donating in nature can donate electron density to the empty p-orbital of the carbene that will be formed, and hence can stabilize the singlet state. For example, phenyldiazirine produces phenylcarbene in the singlet carbene state<ref>{{Cite journal|title = Direct Observation of Carbene and Diazo Formation from Aryldiazirines by Ultrafast Infrared Spectroscopy|journal = Journal of the American Chemical Society|date = 2008-12-03|issn = 0002-7863|pages = 16134–16135|volume = 130|issue = 48|doi = 10.1021/ja805922b|first1 = Yunlong|last1 = Zhang|first2 = Gotard|last2 = Burdzinski|first3 = Jacek|last3 = Kubicki|first4 = Matthew S.|last4 = Platz|pmid=18998681}}</ref> whereas 3-chloro-3-[(4-nitrophenyl)methyl]diazirine or {{chem name|trifluoromethylphenyldiazirine}} produce the respective triplet carbene products.<ref>{{Cite journal|title = Ultrafast Dynamics of Isolated Phenylcarbenes Followed by Femtosecond Time-Resolved Velocity Map Imaging|journal = The Journal of Physical Chemistry A|date = 2009-04-02|issn = 1089-5639|pages = 3041–3050|volume = 113|issue = 13|doi = 10.1021/jp810974m|pmid = 19245233|first1 = Bastian|last1 = Noller|first2 = Lionel|last2 = Poisson|first3 = Raman|last3 = Maksimenka|first4 = Oliver|last4 = Gobert|first5 = Ingo|last5 = Fischer|first6 = J. M.|last6 = Mestdagh|bibcode = 2009JPCA..113.3041N}}</ref><ref>{{Cite journal|title = The photoionisation of two phenylcarbenes and their diazirine precursors investigated using synchrotron radiation|journal = Physical Chemistry Chemical Physics|volume = 11|issue = 26|pages = 5384–5391|doi = 10.1039/b823269e|pmid = 19551206|first1 = Bastian|last1 = Noller|first2 = Patrick|last2 = Hemberger|first3 = Ingo|last3 = Fischer|first4 = Christian|last4 = Alcaraz|first5 = Gustavo A.|last5 = Garcia|first6 = Héloïse|last6 = Soldi-Lose|date = 2009-06-23|bibcode = 2009PCCP...11.5384N|url = https://zenodo.org/record/895863}}</ref>
The substituents on the diazirine affect which carbene species is generated upon irradiation and subsequent photolytic cleavage. Diazirine substituents that are electron donating in nature can donate electron density to the empty p-orbital of the carbene that will be formed, and hence can stabilize the singlet state. For example, phenyldiazirine produces phenylcarbene in the singlet carbene state<ref>{{Cite journal|title = Direct Observation of Carbene and Diazo Formation from Aryldiazirines by Ultrafast Infrared Spectroscopy|journal = Journal of the American Chemical Society|date = 2008-12-03|issn = 0002-7863|pages = 16134–16135|volume = 130|issue = 48|doi = 10.1021/ja805922b|first1 = Yunlong|last1 = Zhang|first2 = Gotard|last2 = Burdzinski|first3 = Jacek|last3 = Kubicki|first4 = Matthew S.|last4 = Platz|pmid=18998681}}</ref> whereas 3-chloro-3-[(4-nitrophenyl)methyl]diazirine or {{chem name|trifluoromethylphenyldiazirine}} produce the respective triplet carbene products.<ref>{{Cite journal|title = Ultrafast Dynamics of Isolated Phenylcarbenes Followed by Femtosecond Time-Resolved Velocity Map Imaging|journal = The Journal of Physical Chemistry A|date = 2009-04-02|issn = 1089-5639|pages = 3041–3050|volume = 113|issue = 13|doi = 10.1021/jp810974m|pmid = 19245233|first1 = Bastian|last1 = Noller|first2 = Lionel|last2 = Poisson|first3 = Raman|last3 = Maksimenka|first4 = Oliver|last4 = Gobert|first5 = Ingo|last5 = Fischer|first6 = J. M.|last6 = Mestdagh|bibcode = 2009JPCA..113.3041N}}</ref><ref>{{Cite journal|title = The photoionisation of two phenylcarbenes and their diazirine precursors investigated using synchrotron radiation|journal = Physical Chemistry Chemical Physics|volume = 11|issue = 26|pages = 5384–5391|doi = 10.1039/b823269e|pmid = 19551206|first1 = Bastian|last1 = Noller|first2 = Patrick|last2 = Hemberger|first3 = Ingo|last3 = Fischer|first4 = Christian|last4 = Alcaraz|first5 = Gustavo A.|last5 = Garcia|first6 = Héloïse|last6 = Soldi-Lose|date = 2009-06-23|bibcode = 2009PCCP...11.5384N|url = https://zenodo.org/record/895863}}</ref>


Electron donating substituents can also encourage photoisomerization to the linear diazo compound <sup>[30]</sup>, rather than the singlet carbene, and hence these compounds are unfavorable for use in biological assays.<ref name=":4" /> On the other hand, {{chem name|trifluoroaryldiazirines}} in particular show favorable stability and photolytic qualities<ref name=":4">{{Cite journal|title = 3-Trifluoromethyl-3-phenyldiazirine. A new carbene generating group for photolabeling reagents|journal = The Journal of Biological Chemistry|date = 1980-04-25|issn = 0021-9258|pmid = 7364745|pages = 3313–3318|volume = 255|issue = 8|first1 = J.|last1 = Brunner|first2 = H.|last2 = Senn|first3 = F. M.|last3 = Richards|doi = 10.1016/S0021-9258(19)85701-0|doi-access = free}}</ref> and are most commonly used in biological applications.<ref name=":0" /> [[File:Screen Shot 2015-12-01 at 3.56.20 PM.png|thumb|281x281px|Three diazirines are shown above. Phenyldiazirine produces the singlet carbene whereas trifluoromethylphenyldiazirine and 3-chloro-3-[(4-nitrophenyl)methyl]diazirine produce triplet state carbenes.|centre]]Carbenes produced from diazirines are quickly quenched by reaction with water molecules,<ref>{{Cite journal|title = Influence of Solvent on Carbene Intersystem Crossing Rates|journal = Journal of the American Chemical Society|date = 2008-05-01|issn = 0002-7863|pages = 6604–6609|volume = 130|issue = 20|doi = 10.1021/ja711385t|first1 = Jin|last1 = Wang|first2 = Jacek|last2 = Kubicki|first3 = Huolei|last3 = Peng|first4 = Matthew S.|last4 = Platz|pmid=18433130}}</ref> and hence yields for photoreactive crosslinking assays are often low. Yet, as this feature minimizes unspecific labeling, it is actually an advantage of using diazirines.
Electron donating substituents can also encourage photoisomerization to the linear diazo compound,<ref>{{Cite journal |last=Korneev |first=Sergei M. |date=November 2011 |title=Valence Isomerization between Diazo Compounds and Diazirines |url=https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201100224 |journal=European Journal of Organic Chemistry |language=en |volume=2011 |issue=31 |pages=6153–6175 |doi=10.1002/ejoc.201100224 |issn=1434-193X}}</ref> rather than the singlet carbene, and hence these compounds are unfavorable for use in biological assays.<ref name=":4" /> On the other hand, {{chem name|trifluoroaryldiazirines}} in particular show favorable stability and photolytic qualities<ref name=":4">{{Cite journal|title = 3-Trifluoromethyl-3-phenyldiazirine. A new carbene generating group for photolabeling reagents|journal = The Journal of Biological Chemistry|date = 1980-04-25|issn = 0021-9258|pmid = 7364745|pages = 3313–3318|volume = 255|issue = 8|first1 = J.|last1 = Brunner|first2 = H.|last2 = Senn|first3 = F. M.|last3 = Richards|doi = 10.1016/S0021-9258(19)85701-0|doi-access = free}}</ref> and are most commonly used in biological applications.<ref name=":0" /> [[File:Screen Shot 2015-12-01 at 3.56.20 PM.png|thumb|281x281px|Three diazirines are shown above. Phenyldiazirine produces the singlet carbene whereas trifluoromethylphenyldiazirine and 3-chloro-3-[(4-nitrophenyl)methyl]diazirine produce triplet state carbenes.|centre]]Carbenes produced from diazirines are quickly quenched by reaction with water molecules,<ref>{{Cite journal|title = Influence of Solvent on Carbene Intersystem Crossing Rates|journal = Journal of the American Chemical Society|date = 2008-05-01|issn = 0002-7863|pages = 6604–6609|volume = 130|issue = 20|doi = 10.1021/ja711385t|first1 = Jin|last1 = Wang|first2 = Jacek|last2 = Kubicki|first3 = Huolei|last3 = Peng|first4 = Matthew S.|last4 = Platz|pmid=18433130}}</ref> and hence yields for photoreactive crosslinking assays are often low. Yet, as this feature minimizes unspecific labeling, it is actually an advantage of using diazirines.


== Use in photoreactive crosslinking ==
== Use in photoreactive crosslinking ==
Diazirines are often used as photoreactive crosslinking reagents, as the reactive carbenes they form upon irradiation with UV light can insert into C-H, N-H, and O-H bonds. This results in proximity-dependent labeling of other species with the diazirine containing compound. However, studies have found that diazirines have some pH dependence in labeling preferences, favoring acidic residues such as glutamate.<ref>{{Cite journal |last1=West |first1=Alexander V. |last2=Muncipinto |first2=Giovanni |last3=Wu |first3=Hung-Yi |last4=Huang |first4=Andrew C. |last5=Labenski |first5=Matthew T. |last6=Jones |first6=Lyn H. |last7=Woo |first7=Christina M. |date=2021-05-05 |title=Labeling Preferences of Diazirines with Protein Biomolecules |url=https://pubs.acs.org/doi/10.1021/jacs.1c02509 |journal=Journal of the American Chemical Society |language=en |volume=143 |issue=17 |pages=6691–6700 |doi=10.1021/jacs.1c02509 |pmid=33876925 |issn=0002-7863}}</ref> Diazirine variants have been developed to reduce this bias.<ref>{{Cite journal |last1=West |first1=Alexander V. |last2=Amako |first2=Yuka |last3=Woo |first3=Christina M. |date=2022-11-23 |title=Design and Evaluation of a Cyclobutane Diazirine Alkyne Tag for Photoaffinity Labeling in Cells |url=https://pubs.acs.org/doi/10.1021/jacs.2c08257 |journal=Journal of the American Chemical Society |language=en |volume=144 |issue=46 |pages=21174–21183 |doi=10.1021/jacs.2c08257 |pmid=36350779 |issn=0002-7863}}</ref>
Diazirines are often used as photoreactive crosslinking reagents, as the reactive carbenes they form upon irradiation with UV light can insert into C-H, N-H, and O-H bonds. This results in proximity dependent labeling of other species with the diazirine containing compound.


Diazirines are often preferred to other photoreactive crosslinking reagents due to their smaller size, longer irradiation wavelength, short period of irradiation required, and stability in the presence of various nucleophiles, and in both acidic and basic conditions.<ref>{{Cite journal|title = Photoaffinity labeling in drug discovery and developments: chemical gateway for entering proteomic frontier|journal = Current Topics in Medicinal Chemistry|date = 2002-03-01|issn = 1568-0266|pmid = 11944820|pages = 271–288|volume = 2|issue = 3|first1 = Yasumaru|last1 = Hatanaka|first2 = Yutaka|last2 = Sadakane|doi=10.2174/1568026023394182}}</ref> [[Benzophenone]]s, which form reactive triplet carbonyl species upon irradiation, often require long periods of irradiation which can result in non-specific labeling, and moreover are often inert to various polar solvents.<ref>{{Cite journal|title = Benzophenone Photoprobes for Phosphoinositides, Peptides and Drugs|journal = Photochemistry and Photobiology|date = 1997-02-01|issn = 1751-1097|pages = 222–234|volume = 65|issue = 2|doi = 10.1111/j.1751-1097.1997.tb08548.x|first1 = Glenn D.|last1 = Prestwich|first2 = György|last2 = Dormán|first3 = John T.|last3 = Elliott|first4 = Dale M.|last4 = Marecak|first5 = Anu|last5 = Chaudhary|pmid = 9066302|s2cid = 12577596}}</ref> Aryl azides require a low wavelength of irradiation, which can damage the biological macromolecules under investigation.
Diazirines are often preferred to other photoreactive crosslinking reagents due to their smaller size, longer irradiation wavelength, short period of irradiation required, and stability in the presence of various nucleophiles, and in both acidic and basic conditions.<ref>{{Cite journal|title = Photoaffinity labeling in drug discovery and developments: chemical gateway for entering proteomic frontier|journal = Current Topics in Medicinal Chemistry|date = 2002-03-01|issn = 1568-0266|pmid = 11944820|pages = 271–288|volume = 2|issue = 3|first1 = Yasumaru|last1 = Hatanaka|first2 = Yutaka|last2 = Sadakane|doi=10.2174/1568026023394182}}</ref> [[Benzophenone]]s, which form reactive triplet carbonyl species upon irradiation, often require long periods of irradiation which can result in non-specific labeling, and moreover are often inert to various polar solvents.<ref>{{Cite journal|title = Benzophenone Photoprobes for Phosphoinositides, Peptides and Drugs|journal = Photochemistry and Photobiology|date = 1997-02-01|issn = 1751-1097|pages = 222–234|volume = 65|issue = 2|doi = 10.1111/j.1751-1097.1997.tb08548.x|first1 = Glenn D.|last1 = Prestwich|first2 = György|last2 = Dormán|first3 = John T.|last3 = Elliott|first4 = Dale M.|last4 = Marecak|first5 = Anu|last5 = Chaudhary|pmid = 9066302|s2cid = 12577596}}</ref> Aryl azides require a low wavelength of irradiation, which can damage the biological macromolecules under investigation.
Line 87: Line 87:
* The synthesis of a diazirine containing analog of [[etoposide]], a widely used cancer drug targeting [[Type II topoisomerase|topoisomerase II]], which holds promise for the identification of the etoposide binding site.<ref>{{Cite journal|title = A diazirine-based photoaffinity etoposide probe for labeling topoisomerase II|journal = Bioorganic & Medicinal Chemistry|date = 2010-01-15|pmc = 2818565|pmid = 20006518|pages = 830–838|volume = 18|issue = 2|doi = 10.1016/j.bmc.2009.11.048|first1 = Gaik-Lean|last1 = Chee|first2 = Jack C.|last2 = Yalowich|first3 = Andrew|last3 = Bodner|first4 = Xing|last4 = Wu|first5 = Brian B.|last5 = Hasinoff}}</ref>[[File:1-s2.0-S0968089611005062-gr27.png|centre|thumb]]
* The synthesis of a diazirine containing analog of [[etoposide]], a widely used cancer drug targeting [[Type II topoisomerase|topoisomerase II]], which holds promise for the identification of the etoposide binding site.<ref>{{Cite journal|title = A diazirine-based photoaffinity etoposide probe for labeling topoisomerase II|journal = Bioorganic & Medicinal Chemistry|date = 2010-01-15|pmc = 2818565|pmid = 20006518|pages = 830–838|volume = 18|issue = 2|doi = 10.1016/j.bmc.2009.11.048|first1 = Gaik-Lean|last1 = Chee|first2 = Jack C.|last2 = Yalowich|first3 = Andrew|last3 = Bodner|first4 = Xing|last4 = Wu|first5 = Brian B.|last5 = Hasinoff}}</ref>[[File:1-s2.0-S0968089611005062-gr27.png|centre|thumb]]
* The discovery that caprolactam-type gamma-secretase inhibitors target the SPP subunit of the [[amyloid precursor protein secretase|gamma-secretase]], which has been implicated in Alzheimer's disease.<ref>{{Cite journal|title = Divergent Synthesis of Multifunctional Molecular Probes To Elucidate the Enzyme Specificity of Dipeptidic γ-Secretase Inhibitors|journal = ACS Chemical Biology|date = 2007-06-01|issn = 1554-8929|pages = 408–418|volume = 2|issue = 6|doi = 10.1021/cb700073y|pmid = 17530731|first1 = Haruhiko|last1 = Fuwa|first2 = Yasuko|last2 = Takahashi|first3 = Yu|last3 = Konno|first4 = Naoto|last4 = Watanabe|first5 = Hiroyuki|last5 = Miyashita|first6 = Makoto|last6 = Sasaki|first7 = Hideaki|last7 = Natsugari|first8 = Toshiyuki|last8 = Kan|first9 = Tohru|last9 = Fukuyama}}</ref>
* The discovery that caprolactam-type gamma-secretase inhibitors target the SPP subunit of the [[amyloid precursor protein secretase|gamma-secretase]], which has been implicated in Alzheimer's disease.<ref>{{Cite journal|title = Divergent Synthesis of Multifunctional Molecular Probes To Elucidate the Enzyme Specificity of Dipeptidic γ-Secretase Inhibitors|journal = ACS Chemical Biology|date = 2007-06-01|issn = 1554-8929|pages = 408–418|volume = 2|issue = 6|doi = 10.1021/cb700073y|pmid = 17530731|first1 = Haruhiko|last1 = Fuwa|first2 = Yasuko|last2 = Takahashi|first3 = Yu|last3 = Konno|first4 = Naoto|last4 = Watanabe|first5 = Hiroyuki|last5 = Miyashita|first6 = Makoto|last6 = Sasaki|first7 = Hideaki|last7 = Natsugari|first8 = Toshiyuki|last8 = Kan|first9 = Tohru|last9 = Fukuyama}}</ref>
* The finding that the [[O-GlcNAc]] [[post-translational modification]] mediates protein-protein interactions such as with [[14-3-3 protein|14-3-3 proteins]].<ref>{{Cite journal |last1=Yu |first1=Seok-Ho |last2=Boyce |first2=Michael |last3=Wands |first3=Amberlyn M. |last4=Bond |first4=Michelle R. |last5=Bertozzi |first5=Carolyn R. |last6=Kohler |first6=Jennifer J. |date=2012-03-27 |title=Metabolic labeling enables selective photocrosslinking of O-GlcNAc-modified proteins to their binding partners |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=109 |issue=13 |pages=4834–4839 |doi=10.1073/pnas.1114356109 |doi-access=free |issn=1091-6490 |pmc=3323966 |pmid=22411826}}</ref><ref>{{Cite journal |last1=Toleman |first1=Clifford A. |last2=Schumacher |first2=Maria A. |last3=Yu |first3=Seok-Ho |last4=Zeng |first4=Wenjie |last5=Cox |first5=Nathan J. |last6=Smith |first6=Timothy J. |last7=Soderblom |first7=Erik J. |last8=Wands |first8=Amberlyn M. |last9=Kohler |first9=Jennifer J. |last10=Boyce |first10=Michael |date=2021-05-20 |title=Structural basis of O-GlcNAc recognition by mammalian 14-3-3 proteins |journal=Proceedings of the National Academy of Sciences of the United States of America |language=en |volume=115 |issue=23 |pages=5956–5961 |doi=10.1073/pnas.1722437115 |doi-access=free |pmc=6003352 |pmid=29784830}}</ref>


=== Examples in nucleic acid studies ===
=== Examples in nucleic acid studies ===
Line 96: Line 97:


== References ==
== References ==
{{reflist}}
{{reflist}}30. S. M. Korneev: ''Valence Isomerization between Diazo Compounds and Diazirines''. In: ''Eur. J. Org. Chem.'' (2011), Band 31, S. 6153–6175, doi:10.1002/ejoc.201100224
[[Category:Nitrogen heterocycles]]
[[Category:Nitrogen heterocycles]]
[[Category:Photochemistry]]
[[Category:Photochemistry]]

Latest revision as of 17:42, 1 November 2024

Not to be confused with Diaziridine.
Diazirine
Identifiers
3D model (JSmol)
605387
ChEBI
ChemSpider
  • InChI=1S/CH2N2/c1-2-3-1/h1H2
    Key: GKVDXUXIAHWQIK-UHFFFAOYSA-N
  • 3H: C1N=N1
Properties
CH2N2
Molar mass 42.041 g·mol−1
Related compounds
Related compounds
 1H-Diazirine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
A generic diazirine

In organic chemistry, diazirines are a class of organic molecules consisting of a carbon bound to two nitrogen atoms, which are double-bonded to each other, forming a cyclopropene-like ring, 3H-diazirine (>CN2). They are isomeric with diazocarbon groups (>C=N=N), and like them can serve as precursors for carbenes by loss of a molecule of dinitrogen. For example, irradiation of diazirines with ultraviolet light leads to carbene insertion into various C−H, N−H, and O−H bonds.[1] Hence, diazirines have grown in popularity as small, photo-reactive, crosslinking reagents.[2] They are often used in photoaffinity labeling studies to observe a variety of interactions, including ligand-receptor, ligand-enzyme, protein-protein, and protein-nucleic acid interactions.[3]

Synthesis

[edit]

A number of methods exist in the literature for the preparation of diazirines, which begin from a variety of reagents.[4]

Synthesis from ketones

[edit]

Generally, synthetic schemes that begin with ketones (>C=O) involve conversion of the ketone with the desired substituents to diaziridines (>CN2H2). These diaziridines are then subsequently oxidized to form the desired diazirines.

Diaziridines can be prepared from ketones by oximation, followed by tosylation (or mesylation), and then finally by treatment with ammonia (NH3). Generally, oximation reactions are performed by reacting the ketone with hydroxylammonium chloride (NH3OH−Cl+) under heat in the presence of a base such as pyridine.[5][6] Subsequent tosylation or mesylation of the alpha-substituted oxygen with tosyl or mesyl chloride in the presence of base yields the tosyl or mesyl oxime.[7] The final treatment of the tosyl or mesyl oxime with ammonia produces the diaziridine.[1][3][7][8]

Generic diaziridine synthesis by oximation, tosylation, and treatment with ammonia.

Diaziridines can be also produced directly by the reaction of ketones with ammonia in the presence of an aminating agent such as a monochloramine or hydroxyl amine O-sulfonic acid.[9]

Diaziridines can be oxidized to diazirines by a number of methods. These include oxidation by chromium-based reagents such as the Jones oxidation,[10] oxidation by iodine and triethylamine,[5] oxidation by silver oxide,[11] oxidation by oxalyl chloride,[7] or even electrochemical oxidation on a platinum-titanium anode.[12]

Jones oxidation of a generic diaziridine to a diazirine.

Synthesis by Graham reaction

[edit]

Diazirines can be alternatively formed in a one-pot process using the Graham reaction, starting from amidines.[13] This reaction yields a halogenated diazirine, whose halogen can be displaced by various nucleophilic reagents.[14]

The Graham reaction as a method of diazirine synthesis, where X = Cl or Br.
The diazirine exchange reaction using various anions and the counterion tetra-n-butylammonium.

Chemistry

[edit]

Upon irradiation with UV light, diazirines form reactive carbene species. The carbene may exist in the singlet form, in which the two free electrons occupy the same orbital, or the triplet form, with two unpaired electrons in different orbitals.

Diazirines can be decomposed by using UV-light.

Triplet vs singlet carbene products

[edit]

The substituents on the diazirine affect which carbene species is generated upon irradiation and subsequent photolytic cleavage. Diazirine substituents that are electron donating in nature can donate electron density to the empty p-orbital of the carbene that will be formed, and hence can stabilize the singlet state. For example, phenyldiazirine produces phenylcarbene in the singlet carbene state[15] whereas 3-chloro-3-[(4-nitrophenyl)methyl]diazirine or trifluoromethylphenyldiazirine produce the respective triplet carbene products.[16][17]

Electron donating substituents can also encourage photoisomerization to the linear diazo compound,[18] rather than the singlet carbene, and hence these compounds are unfavorable for use in biological assays.[19] On the other hand, trifluoroaryldiazirines in particular show favorable stability and photolytic qualities[19] and are most commonly used in biological applications.[1]

Three diazirines are shown above. Phenyldiazirine produces the singlet carbene whereas trifluoromethylphenyldiazirine and 3-chloro-3-[(4-nitrophenyl)methyl]diazirine produce triplet state carbenes.

Carbenes produced from diazirines are quickly quenched by reaction with water molecules,[20] and hence yields for photoreactive crosslinking assays are often low. Yet, as this feature minimizes unspecific labeling, it is actually an advantage of using diazirines.

Use in photoreactive crosslinking

[edit]

Diazirines are often used as photoreactive crosslinking reagents, as the reactive carbenes they form upon irradiation with UV light can insert into C-H, N-H, and O-H bonds. This results in proximity-dependent labeling of other species with the diazirine containing compound. However, studies have found that diazirines have some pH dependence in labeling preferences, favoring acidic residues such as glutamate.[21] Diazirine variants have been developed to reduce this bias.[22]

Diazirines are often preferred to other photoreactive crosslinking reagents due to their smaller size, longer irradiation wavelength, short period of irradiation required, and stability in the presence of various nucleophiles, and in both acidic and basic conditions.[23] Benzophenones, which form reactive triplet carbonyl species upon irradiation, often require long periods of irradiation which can result in non-specific labeling, and moreover are often inert to various polar solvents.[24] Aryl azides require a low wavelength of irradiation, which can damage the biological macromolecules under investigation.

Examples in receptor labeling studies

[edit]

Diazirines are widely used in receptor labeling studies. This is because diazirine-containing analogs of various ligands can be synthesized and incubated with their respective receptors, and then subsequently exposed to light to produce reactive carbenes. The carbene will covalently bond to residues in the binding site of the receptor. The carbene compound may include a bioorthogonal tag or handle by which the protein of interest can be isolated. The protein can then be digested and sequenced by mass spectrometry in order to identify which residues the carbene containing ligand is bound to, and hence the identity of the binding site in the receptor.

Examples of diazirines used in receptor labeling studies include:

  • The discovery of a brassinosteroid receptor for brassinosteroid plant hormones by Kinoshita et al. Researchers used a plant hormone analog with a diazirine crosslinking moiety and a biotin tag for isolation to identity the new receptor.[25] This study led to a number of similar studies conducted with regards to other plant hormones.
Propofol (left) and m-azipropofol, a diazirine analog of it

Examples in enzyme-substrate studies

[edit]

In a manner analogous to receptor labeling, diazirine containing compounds that are analogs of natural substrates have also been used to identify binding pockets of enzymes. Examples include:

Examples in nucleic acid studies

[edit]

Diazirines have been used in photoaffinity labeling experiments involving nucleic acids as well. Examples include:

  • Incorporation of a diazirine moiety on a nucleoside sugar in a DNA polymer to investigate interactions between the minor groove of DNA and DNA polymerases.[32]
  • Incorporation of a diazirine moiety on a nucleoside base in a DNA polymer to investigate the mode of DNA repair by proteins.[33]

Diazirines have also been used to study protein lipid interactions, for example the interaction of various sphingolipids with proteins in vivo.[34]

References

[edit]
  1. ^ a b c Dubinsky, Luba; Krom, Bastiaan P.; Meijler, Michael M. (2012-01-15). "Diazirine based photoaffinity labeling". Bioorganic & Medicinal Chemistry. Chemical Proteomics. 20 (2): 554–570. doi:10.1016/j.bmc.2011.06.066. PMID 21778062.
  2. ^ Hill, James R.; Robertson, Avril A. B. (2018). "Fishing for Drug Targets: A Focus on Diazirine Photoaffinity Probe Synthesis". Journal of Medicinal Chemistry. 61 (16): 6945–6963. doi:10.1021/acs.jmedchem.7b01561. PMID 29683660.
  3. ^ a b Sinz, Andrea (2007-04-01). "Investigation of protein-ligand interactions by mass spectrometry". ChemMedChem. 2 (4): 425–431. doi:10.1002/cmdc.200600298. ISSN 1860-7187. PMID 17299828. S2CID 23769515.
  4. ^ Hill, James R.; Robertson, Avril A. B. (2018). "Fishing for Drug Targets: A Focus on Diazirine Photoaffinity Probe Synthesis". Journal of Medicinal Chemistry. 61 (16): 6945–6963. doi:10.1021/acs.jmedchem.7b01561. PMID 29683660.
  5. ^ a b Burkard, Nadja; Bender, Tobias; Westmeier, Johannes; Nardmann, Christin; Huss, Markus; Wieczorek, Helmut; Grond, Stephanie; von Zezschwitz, Paultheo (2010-04-01). "New Fluorous Photoaffinity Labels (F-PAL) and Their Application in V-ATPase Inhibition Studies". European Journal of Organic Chemistry. 2010 (11): 2176–2181. doi:10.1002/ejoc.200901463. ISSN 1099-0690.
  6. ^ Song, Zhiquan; Zhang, Qisheng (2009-11-05). "Fluorous Aryldiazirine Photoaffinity Labeling Reagents". Organic Letters. 11 (21): 4882–4885. doi:10.1021/ol901955y. ISSN 1523-7060. PMID 19807115.
  7. ^ a b c Kumar, Nag S.; Young, Robert N. (2009-08-01). "Design and synthesis of an all-in-one 3-(1,1-difluoroprop-2-ynyl)-3H-diazirin-3-yl functional group for photo-affinity labeling". Bioorganic & Medicinal Chemistry. 17 (15): 5388–5395. doi:10.1016/j.bmc.2009.06.048. PMID 19604700.
  8. ^ Gu, Min; Yan, Jianbin; Bai, Zhiyan; Chen, Yue-Ting; Lu, Wei; Tang, Jie; Duan, Liusheng; Xie, Daoxin; Nan, Fa-Jun (2010-05-01). "Design and synthesis of biotin-tagged photoaffinity probes of jasmonates". Bioorganic & Medicinal Chemistry. 18 (9): 3012–3019. doi:10.1016/j.bmc.2010.03.059. PMID 20395151.
  9. ^ Dubinsky, Luba; Jarosz, Lucja M.; Amara, Neri; Krief, Pnina; Kravchenko, Vladimir V.; Krom, Bastiaan P.; Meijler, Michael M. (2009-11-24). "Synthesis and validation of a probe to identify quorum sensing receptors". Chemical Communications (47): 7378–7380. doi:10.1039/b917507e. PMID 20024234.
  10. ^ Wagner, Gerald; Knoll, Wolfgang; Bobek, Michael M.; Brecker, Lothar; van Herwijnen, Hendrikus W. G.; Brinker, Udo H. (2010-01-15). "Structure−Reactivity Relationships: Reactions of a 5-Substituted Aziadamantane in a Resorcin[4]arene-based Cavitand". Organic Letters. 12 (2): 332–335. doi:10.1021/ol902667a. ISSN 1523-7060. PMID 20017550.
  11. ^ Al-Omari, Mohammad; Banert, Klaus; Hagedorn, Manfred (2006-01-01). "Bi-3H-diazirin-3-yls as Precursors of Highly Strained Cycloalkynes". Angewandte Chemie International Edition. 45 (2): 309–311. doi:10.1002/anie.200503124. ISSN 1521-3773. PMID 16372311.
  12. ^ Vedenyapina, M. D.; Kuznetsov, V. V.; Nizhnikovskii, E. A.; Strel’tsova, E. D.; Makhova, N. N.; Struchkova, M. I.; Vedenyapin, A. A. (2006-11-01). "Electrochemical synthesis of pentamethylenediazirine". Russian Chemical Bulletin. 55 (11): 2013–2015. doi:10.1007/s11172-006-0544-0. ISSN 1066-5285. S2CID 97472127.
  13. ^ Graham, W. H. (1965-10-01). "The Halogenation of Amidines. I. Synthesis of 3-Halo- and Other Negatively Substituted Diazirines1". Journal of the American Chemical Society. 87 (19): 4396–4397. doi:10.1021/ja00947a040. ISSN 0002-7863.
  14. ^ Moss, Robert A. (2006-02-09). "Diazirines: Carbene Precursors Par Excellence". Accounts of Chemical Research. 39 (4): 267–272. doi:10.1021/ar050155h. ISSN 0001-4842. PMID 16618094.
  15. ^ Zhang, Yunlong; Burdzinski, Gotard; Kubicki, Jacek; Platz, Matthew S. (2008-12-03). "Direct Observation of Carbene and Diazo Formation from Aryldiazirines by Ultrafast Infrared Spectroscopy". Journal of the American Chemical Society. 130 (48): 16134–16135. doi:10.1021/ja805922b. ISSN 0002-7863. PMID 18998681.
  16. ^ Noller, Bastian; Poisson, Lionel; Maksimenka, Raman; Gobert, Oliver; Fischer, Ingo; Mestdagh, J. M. (2009-04-02). "Ultrafast Dynamics of Isolated Phenylcarbenes Followed by Femtosecond Time-Resolved Velocity Map Imaging". The Journal of Physical Chemistry A. 113 (13): 3041–3050. Bibcode:2009JPCA..113.3041N. doi:10.1021/jp810974m. ISSN 1089-5639. PMID 19245233.
  17. ^ Noller, Bastian; Hemberger, Patrick; Fischer, Ingo; Alcaraz, Christian; Garcia, Gustavo A.; Soldi-Lose, Héloïse (2009-06-23). "The photoionisation of two phenylcarbenes and their diazirine precursors investigated using synchrotron radiation". Physical Chemistry Chemical Physics. 11 (26): 5384–5391. Bibcode:2009PCCP...11.5384N. doi:10.1039/b823269e. PMID 19551206.
  18. ^ Korneev, Sergei M. (November 2011). "Valence Isomerization between Diazo Compounds and Diazirines". European Journal of Organic Chemistry. 2011 (31): 6153–6175. doi:10.1002/ejoc.201100224. ISSN 1434-193X.
  19. ^ a b Brunner, J.; Senn, H.; Richards, F. M. (1980-04-25). "3-Trifluoromethyl-3-phenyldiazirine. A new carbene generating group for photolabeling reagents". The Journal of Biological Chemistry. 255 (8): 3313–3318. doi:10.1016/S0021-9258(19)85701-0. ISSN 0021-9258. PMID 7364745.
  20. ^ Wang, Jin; Kubicki, Jacek; Peng, Huolei; Platz, Matthew S. (2008-05-01). "Influence of Solvent on Carbene Intersystem Crossing Rates". Journal of the American Chemical Society. 130 (20): 6604–6609. doi:10.1021/ja711385t. ISSN 0002-7863. PMID 18433130.
  21. ^ West, Alexander V.; Muncipinto, Giovanni; Wu, Hung-Yi; Huang, Andrew C.; Labenski, Matthew T.; Jones, Lyn H.; Woo, Christina M. (2021-05-05). "Labeling Preferences of Diazirines with Protein Biomolecules". Journal of the American Chemical Society. 143 (17): 6691–6700. doi:10.1021/jacs.1c02509. ISSN 0002-7863. PMID 33876925.
  22. ^ West, Alexander V.; Amako, Yuka; Woo, Christina M. (2022-11-23). "Design and Evaluation of a Cyclobutane Diazirine Alkyne Tag for Photoaffinity Labeling in Cells". Journal of the American Chemical Society. 144 (46): 21174–21183. doi:10.1021/jacs.2c08257. ISSN 0002-7863. PMID 36350779.
  23. ^ Hatanaka, Yasumaru; Sadakane, Yutaka (2002-03-01). "Photoaffinity labeling in drug discovery and developments: chemical gateway for entering proteomic frontier". Current Topics in Medicinal Chemistry. 2 (3): 271–288. doi:10.2174/1568026023394182. ISSN 1568-0266. PMID 11944820.
  24. ^ Prestwich, Glenn D.; Dormán, György; Elliott, John T.; Marecak, Dale M.; Chaudhary, Anu (1997-02-01). "Benzophenone Photoprobes for Phosphoinositides, Peptides and Drugs". Photochemistry and Photobiology. 65 (2): 222–234. doi:10.1111/j.1751-1097.1997.tb08548.x. ISSN 1751-1097. PMID 9066302. S2CID 12577596.
  25. ^ Kinoshita, Toshinori; Caño-Delgado, Ana; Seto, Hideharu; Hiranuma, Sayoko; Fujioka, Shozo; Yoshida, Shigeo; Chory, Joanne (2005). "Binding of brassinosteroids to the extracellular domain of plant receptor kinase BRI1". Nature. 433 (7022): 167–171. Bibcode:2005Natur.433..167K. doi:10.1038/nature03227. PMID 15650741. S2CID 4379617.
  26. ^ Balas, Laurence; Durand, Thierry; Saha, Sattyabrata; Johnson, Inneke; Mukhopadhyay, Somnath (2009-02-26). "Total Synthesis of Photoactivatable or Fluorescent Anandamide Probes: Novel Bioactive Compounds with Angiogenic Activity". Journal of Medicinal Chemistry. 52 (4): 1005–1017. doi:10.1021/jm8011382. ISSN 0022-2623. PMID 19161308.
  27. ^ Hall, Michael A.; Xi, Jin; Lor, Chong; Dai, Shuiping; Pearce, Robert; Dailey, William P.; Eckenhoff, Roderic G. (2010-08-12). "m-Azipropofol (AziPm) a Photoactive Analogue of the Intravenous General Anesthetic Propofol". Journal of Medicinal Chemistry. 53 (15): 5667–5675. doi:10.1021/jm1004072. ISSN 0022-2623. PMC 2917171. PMID 20597506.
  28. ^ Chee, Gaik-Lean; Yalowich, Jack C.; Bodner, Andrew; Wu, Xing; Hasinoff, Brian B. (2010-01-15). "A diazirine-based photoaffinity etoposide probe for labeling topoisomerase II". Bioorganic & Medicinal Chemistry. 18 (2): 830–838. doi:10.1016/j.bmc.2009.11.048. PMC 2818565. PMID 20006518.
  29. ^ Fuwa, Haruhiko; Takahashi, Yasuko; Konno, Yu; Watanabe, Naoto; Miyashita, Hiroyuki; Sasaki, Makoto; Natsugari, Hideaki; Kan, Toshiyuki; Fukuyama, Tohru (2007-06-01). "Divergent Synthesis of Multifunctional Molecular Probes To Elucidate the Enzyme Specificity of Dipeptidic γ-Secretase Inhibitors". ACS Chemical Biology. 2 (6): 408–418. doi:10.1021/cb700073y. ISSN 1554-8929. PMID 17530731.
  30. ^ Yu, Seok-Ho; Boyce, Michael; Wands, Amberlyn M.; Bond, Michelle R.; Bertozzi, Carolyn R.; Kohler, Jennifer J. (2012-03-27). "Metabolic labeling enables selective photocrosslinking of O-GlcNAc-modified proteins to their binding partners". Proceedings of the National Academy of Sciences of the United States of America. 109 (13): 4834–4839. doi:10.1073/pnas.1114356109. ISSN 1091-6490. PMC 3323966. PMID 22411826.
  31. ^ Toleman, Clifford A.; Schumacher, Maria A.; Yu, Seok-Ho; Zeng, Wenjie; Cox, Nathan J.; Smith, Timothy J.; Soderblom, Erik J.; Wands, Amberlyn M.; Kohler, Jennifer J.; Boyce, Michael (2021-05-20). "Structural basis of O-GlcNAc recognition by mammalian 14-3-3 proteins". Proceedings of the National Academy of Sciences of the United States of America. 115 (23): 5956–5961. doi:10.1073/pnas.1722437115. PMC 6003352. PMID 29784830.
  32. ^ Liebmann, Meike; Di Pasquale, Francesca; Marx, Andreas (2006-12-04). "A New Photoactive Building Block for Investigation of DNA Backbone Interactions: Photoaffinity Labeling of Human DNA Polymerase β". ChemBioChem. 7 (12): 1965–1969. doi:10.1002/cbic.200600333. ISSN 1439-7633. PMID 17106908. S2CID 22908416.
  33. ^ Winnacker, Malte; Breeger, Sascha; Strasser, Ralf; Carell, Thomas (2009-01-05). "Novel Diazirine-Containing DNA Photoaffinity Probes for the Investigation of DNA-Protein-Interactions". ChemBioChem. 10 (1): 109–118. doi:10.1002/cbic.200800397. ISSN 1439-7633. PMID 19012292. S2CID 5605171.
  34. ^ Yamamoto, Tetsuya; Hasegawa, Hiroko; Hakogi, Toshikazu; Katsumura, Shigeo (2006-11-01). "Versatile Synthetic Method for Sphingolipids and Functionalized Sphingosine Derivatives via Olefin Cross Metathesis". Organic Letters. 8 (24): 5569–5572. doi:10.1021/ol062258l. ISSN 1523-7060. PMID 17107074.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Diazirine&oldid=1254785610"