Intracellular carbon monoxide release unveils selective antibacterial effects
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Abstract
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OpenAlex topics: Heme Oxygenase-1 and Carbon Monoxide · Thermal Regulation in Medicine · Hemoglobin structure and function
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References (46)
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1. Wu L, Wang R. Carbon monoxide: Endogenous production, physiological functions, and pharmacological applications. Pharmacol Rev, 2005, 57: 585–63010.1124/pr.57.4.3 ↗
2. Motterlini R, Otterbein LE. The therapeutic potential of carbon monoxide. Nat Rev Drug Discov, 2010, 9: 728–74310.1038/nrd3228 ↗
3. Katsnelson A. The good side of carbon monoxide. ACS Cent Sci, 2019, 5: 1632–163510.1021/acscentsci.9b01015 ↗
4. Nobre LS, Seixas JD, Romão CC, et al. Antimicrobial action of carbon monoxide-releasing compounds. Antimicrob Agents Chemother, 2007, 51: 4303–430710.1128/AAC.00802-07 ↗
5. Klinger-Strobel M, Gläser S, Makarewicz O, et al. Bactericidal effect of a photoresponsive carbon monoxide-releasing nonwoven against Staphylococcus aureus biofilms. Antimicrob Agents Chemother, 2016, 60: 4037–404610.1128/AAC.00703-16 ↗
6. Sahlberg Bang C, Kruse R, Johansson K, et al. Carbon monoxide releasing molecule-2 (CORM-2) inhibits growth of multidrug-resistant uropathogenic Escherichia coli in biofilm and following host cell colonization. BMC Microbiol, 2016, 16: 6410.1186/s12866-016-0678-7 ↗
7. Davidge KS, Sanguinetti G, Yee CH, et al. Carbon monoxide-releasing antibacterial molecules target respiration and global transcriptional regulators. J Biol Chem, 2009, 284: 4516–452410.1074/jbc.M808210200 ↗
8. Nguyen D, Nguyen TK, Rice SA, et al. CO-releasing polymers exert antimicrobial activity. Biomacromolecules, 2015, 16: 2776–278610.1021/acs.biomac.5b00716 ↗
9. Desmard M, Foresti R, Morin D, et al. Differential antibacterial activity against Pseudomonas aeruginosa by carbon monoxide-releasing molecules. Antioxid Redox Signal, 2012, 16: 153–16310.1089/ars.2011.3959 ↗
10. Wilson JL, Jesse HE, Hughes B, et al. Ru(CO)3Cl(glycinate) (CORM-3): A carbon monoxide–releasing molecule with broad-spectrum antimicrobial and photosensitive activities against respiration and cation transport in Escherichia coli. Antioxid Redox Signal, 2013, 19: 497–50910.1089/ars.2012.4784 ↗
11. De La Cruz LKC, Benoit SL, Pan Z, et al. Click, release, and fluoresce: A chemical strategy for a cascade prodrug system for codelivery of carbon monoxide, a drug payload, and a fluorescent reporter. Org Lett, 2018, 20: 897–90010.1021/acs.orglett.7b03348 ↗
12. Tripathi R, Yang X, Ryter SW, et al. Carbon monoxide as a therapeutic for airway diseases: Contrast and comparison of various CO delivery modalities. CTMC, 2021, 21: 2890–290810.2174/1568026621666211116090917 ↗
13. Wareham LK, Poole RK, Tinajero-Trejo M. CO-releasing metal carbonyl compounds as antimicrobial agents in the post-antibiotic era. J Biol Chem, 2015, 290: 18999–1900710.1074/jbc.R115.642926 ↗
14. Wegiel B, Larsen R, Gallo D, et al. Macrophages sense and kill bacteria through carbon monoxide–dependent inflammasome activation. J Clin Invest, 2014, 124: 4926–494010.1172/JCI72853 ↗
15. Southam HM, Williamson MP, Chapman JA, et al. ‘Carbon-monoxide-releasing molecule-2 (CORM-2)’ is a misnomer: Ruthenium toxicity, not CO release, accounts for its antimicrobial effects. Antioxidants, 2021, 10: 915–93710.3390/antiox10060915 ↗
16. Southam HM, Smith TW, Lyon RL, et al. A thiol-reactive Ru(II) ion, not CO release, underlies the potent antimicrobial and cytotoxic properties of CO-releasing molecule-3. Redox Biol, 2018, 18: 114–12310.1016/j.redox.2018.06.008 ↗
17. Lazarus LS, Simons CR, Arcidiacono A, et al. Extracellular vs intra-cellular delivery of CO: Does it matter for a stable, diffusible gasotransmitter? J Med Chem, 2019, 62: 9990–999510.1021/acs.jmedchem.9b01254 ↗
18. Antony LAP, Slanina T, Šebej P, et al. Fluorescein analogue xanthene-9-carboxylic acid: A transition-metal-free CO releasing molecule activated by green light. Org Lett, 2013, 15: 4552–455510.1021/ol4021089 ↗
19. Peng P, Wang C, Shi Z, et al. Visible-light activatable organic CO-releasing molecules (PhotoCORMs) that simultaneously generate fluorophores. Org Biomol Chem, 2013, 11: 6671–667410.1039/c3ob41385c ↗
20. Palao E, Slanina T, Muchová L, et al. Transition-metal-free CO-releasing BODIPY derivatives activatable by visible to NIR light as promising bioactive molecules. J Am Chem Soc, 2015, 138: 126–13310.1021/jacs.5b10800 ↗
21. Zheng Y, Ji X, Yu B, et al. Enrichment-triggered prodrug activation demonstrated through mitochondria-targeted delivery of doxorubicin and carbon monoxide. Nat Chem, 2018, 10: 787–79410.1038/s41557-018-0055-2 ↗
22. Popova M, Lazarus LS, Ayad S, et al. Visible-light-activated quinolone carbon-monoxide-releasing molecule: Prodrug and albumin-assisted delivery enables anticancer and potent anti-inflammatory effects. J Am Chem Soc, 2018, 140: 9721–972910.1021/jacs.8b06011 ↗
23. Lazarus LS, Esquer HJ, Benninghoff AD, et al. Sense and release: A thiol-responsive flavonol-based photonically driven carbon monoxide-releasing molecule that operates via a multiple-input AND logic gate. J Am Chem Soc, 2017, 139: 9435–943810.1021/jacs.7b04077 ↗
24. Lazarus LS, Benninghoff AD, Berreau LM. Development of triggerable, trackable, and targetable carbon monoxide releasing molecules. Acc Chem Res, 2020, 53: 2273–228510.1021/acs.accounts.0c00402 ↗
25. Li Y, Shu Y, Liang M, et al. A two-photon H2O2-activated CO photoreleaser. Angew Chem Int Ed, 2018, 57: 12415–1241910.1002/anie.201805806 ↗
26. Anderson SN, Richards JM, Esquer HJ, et al. A structurally-tunable 3-hydroxyflavone motif for visible light-induced carbon monoxide-releasing molecules (CORMs). ChemistryOpen, 2015, 4: 590–59410.1002/open.201500167 ↗
27. Liu C, Du Z, Ma M, et al. Carbon monoxide controllable targeted gas therapy for synergistic anti-inflammation. iScience, 2020, 23: 10148310.1016/j.isci.2020.101483 ↗
28. Min Q, Ni Z, You M, et al. Chemiexcitation-triggered prodrug activation for targeted carbon monoxide delivery. Angew Chem Int Ed, 2022, 61: e20220097410.1002/anie.202200974 ↗
29. Cheng J, Gan G, Shen Z, et al. Red light-triggered intracellular carbon monoxide release enables selective eradication of MRSA infection. Angew Chem Int Ed, 2021, 60: 13513–1352010.1002/anie.202104024 ↗
30. Corrigan N, Jung K, Moad G, et al. Reversible-deactivation radical polymerization (controlled/living radical polymerization): From discovery to materials design and applications. Prog Polym Sci, 2020, 111: 10131110.1016/j.progpolymsci.2020.101311 ↗
31. Moan J, Berg K. The photodegradation of porphyrins in cells can be used to estimate the lifetime of singlet oxygen. Photochem PhotoBiol, 1991, 53: 549–55310.1111/j.1751-1097.1991.tb03669.x ↗
32. Nawaz S, Carbone P. Coarse-graining poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) (PEO–PPO–PEO) block copolymers using the MARTINI force field. J Phys Chem B, 2014, 118: 1648–165910.1021/jp4092249 ↗
33. de Jong DH, Singh G, Bennett WFD, et al. Improved parameters for the martini coarse-grained protein force field. J Chem Theor Comput, 2013, 9: 687–69710.1021/ct300646g ↗
34. Polyansky AA, Ramaswamy R, Volynsky PE, et al. Antimicrobial peptides induce growth of phosphatidylglycerol domains in a model bacterial membrane. J Phys Chem Lett, 2010, 1: 3108–311110.1021/jz101163e ↗
35. Tavares AFN, Teixeira M, Romão CC, et al. Reactive oxygen species mediate bactericidal killing elicited by carbon monoxide-releasing molecules. J Biol Chem, 2011, 286: 26708–2671710.1074/jbc.M111.255752 ↗
36. Li L, Abe Y, Kanagawa K, et al. Distinguishing the 5,5-dimethyl-1-pyrroline N-oxide (DMPO)-OH radical quenching effect from the hydroxyl radical scavenging effect in the ESR spin-trapping method. Anal Chim Acta, 2004, 512: 121–12410.1016/j.aca.2004.02.020 ↗
37. Peralta E, Roa G, Hernandez-Servin JA, et al. Hydroxyl radicals quantification by UV spectrophotometry. Electrochim Acta, 2014, 129: 137–14110.1016/j.electacta.2014.02.047 ↗
38. Zhang LS, Wong KH, Yip HY, et al. Effective photocatalytic disinfection of E. coli K-12 using AgBr–Ag–Bi2WO6 nanojunction system irradiated by visible light: The role of diffusing hydroxyl radicals. Environ Sci Technol, 2010, 44: 1392–139810.1021/es903087w ↗
39. Niu W, Zhang Y, Liu J, et al. OxyR controls magnetosome formation by regulating magnetosome island (MAI) genes, iron metabolism, and redox state. Free Radical Biol Med, 2020, 161: 272–28210.1016/j.freeradbiomed.2020.10.015 ↗
40. Si M, Wang Y, Zhang B, et al. The type VI secretion system engages a redox-regulated dual-functional heme transporter for zinc acquisition. Cell Rep, 2017, 20: 949–95910.1016/j.celrep.2017.06.081 ↗
41. Horsburgh MJ, Tuomanen EI, Clements MO, et al. Perr controls oxidative stress resistance and iron storage proteins and is required for virulence in Staphylococcus aureus. Infect Immun, 2001, 69: 3744–375410.1128/IAI.69.6.3744-3754.2001 ↗
42. Zhao XJ, Raitt D, Burke PV, et al. Function and expression of flavohemoglobin in Saccharomyces cerevisiae. J Biol Chem, 1996, 271: 25131–2513810.1074/jbc.271.41.25131 ↗
43. Mironov A, Seregina T, Shatalin K, et al. CydDC functions as a cytoplasmic cystine reductase to sensitize Escherichia coli to oxidative stress and aminoglycosides. Proc Natl Acad Sci USA, 2020, 117: 23565–2357010.1073/pnas.2007817117 ↗
44. Motterlini R, Foresti R. Biological signaling by carbon monoxide and carbon monoxide-releasing molecules. Am J Physiol Cell Physiol, 2017, 312: C302–C31310.1152/ajpcell.00360.2016 ↗
45. Mansour SC, Pletzer D, de la Fuente-Núñez C, et al. Bacterial abscess formation is controlled by the stringent stress response and can be targeted therapeutically. EBioMedicine, 2016, 12: 219–22610.1016/j.ebiom.2016.09.015 ↗
46. Lei XL, Cheng K, Hu YG, et al. Gelatinase-responsive biodegradable targeted microneedle patch for abscess wound treatment of S. aureus infection. Int J Biol Macromolecules, 2023, 253: 12754810.1016/j.ijbiomac.2023.127548 ↗