Manoj Veleeparambil

ORCID: 0000-0003-3545-5251
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About
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Research Areas
  • Photochemistry and Electron Transfer Studies
  • Advanced oxidation water treatment
  • interferon and immune responses
  • Free Radicals and Antioxidants
  • Nitric Oxide and Endothelin Effects
  • Immune Response and Inflammation
  • Sulfur Compounds in Biology
  • Air Quality Monitoring and Forecasting
  • Viral Infections and Vectors
  • Electron Spin Resonance Studies
  • Air Quality and Health Impacts
  • NF-κB Signaling Pathways
  • DNA and Nucleic Acid Chemistry
  • Cytokine Signaling Pathways and Interactions
  • Environmental remediation with nanomaterials
  • Inflammasome and immune disorders
  • Inflammatory Biomarkers in Disease Prognosis
  • Extracellular vesicles in disease
  • Noise Effects and Management
  • Synthesis and Characterization of Heterocyclic Compounds
  • Energy and Environment Impacts
  • Odor and Emission Control Technologies
  • Pesticide and Herbicide Environmental Studies
  • Steroid Chemistry and Biochemistry
  • Radical Photochemical Reactions

Cleveland Clinic
2012-2023

University of Toledo
2023

Cleveland Clinic Lerner College of Medicine
2011-2021

Vanderbilt University
2013

Environmental and Occupational Health Sciences Institute
2010

Rutgers, The State University of New Jersey
2009

Mahatma Gandhi University
2000-2007

Bhabha Atomic Research Centre
2002-2006

Advanced Materials and Processes Research Institute
2006

California Institute of Technology
2002

Thrombosis is one of the main complications in cancer patients often leading to mortality. However, mechanisms underlying platelet hyperactivation are poorly understood.

10.1161/circresaha.122.321861 article EN Circulation Research 2023-05-05

The interferon (IFN) system represents the first line of defense against a wide range viruses. Virus infection rapidly triggers transcriptional induction IFN-β and IFN Stimulated Genes (ISGs), whose protein products act as viral restriction factors by interfering with specific stages virus life cycle, such entry, transcription, translation, genome replication, assembly egress. Here, we report new mode action an ISG, IFN-induced TDRD7 (tudor domain containing 7) inhibited paramyxovirus...

10.1371/journal.ppat.1006877 article EN cc-by PLoS Pathogens 2018-01-30

For many individuals, daily commuting activities on roadways account for a substantial proportion of total exposure, as well peak-level exposures, to traffic-related air pollutants (TRAPS) including ultrafine particles, but the health impacts these exposures are not well-understood. We sought determine if exposure TRAPs particles during causes acute oxidative stress in respiratory tract or changes heart rate variability (HRV), measure autonomic activity.We conducted randomized, cross-over...

10.1186/s12989-014-0045-5 article EN cc-by Particle and Fibre Toxicology 2014-10-31

Interferon (IFN) is required for protecting mice from viral pathogenesis; reciprocally, it mediates the deleterious septic shock response to bacterial infection. The critical transcription factor IFN induction, in both cases, IRF-3, which activated by TLR3 or RIG-I signaling virus infection and TLR4 Here, we report that IRF-3's transcriptional activity its coactivators, β-catenin CBP, be modified HDAC6-mediated deacetylation protein kinase C isozyme β (PKC-β)-mediated phosphorylation,...

10.1128/mbio.00636-12 article EN mBio 2013-03-27

Infection of cultured cells by paramyxoviruses causes cell death, mediated a newly discovered apoptotic pathway activated virus infection. The key proapoptotic protein in this is interferon regulatory factor 3 (IRF-3), which upon activation infection binds BAX, translocates it to mitochondria, and triggers apoptosis. When IRF-3-knockdown were infected with Sendai (SeV), persistent (PI) was established. PI produced infectious SeV continuously constitutively expressed many innate immune genes....

10.1128/jvi.01853-12 article EN Journal of Virology 2012-10-18

Abstract Laser flash photolysis has been used to determine the bimolecular rate constants and spectral nature of intermediates obtained by reaction sulfate radical anion (SO ) with 1,3,5‐triazine (T), 2,4,6‐trimethoxy‐1,3,5‐triazine (TMT), 2,4‐dioxohexahydro‐1,3,5‐triazine (DHT), 6‐chloro N ‐ethyl N'‐(1‐methylethyl)‐1,3,5‐triazine‐2,4‐diamine (atrazine, AT). The determined were in range 4.6 × 10 7 –3 9 dm 3 mol −1 s at pH 6. transient absorption spectra from SO T, TMT, DHT AT an maximum...

10.1002/poc.1134 article EN Journal of Physical Organic Chemistry 2007-02-01

The innate immune response to virus infection leads interferon production and inhibition of viral replication. STING, an ER-bound protein, mediates such a cytoplasmic cellular or microbial DNA.

10.1128/mbio.03228-21 article EN mBio 2021-12-21

Abstract Mammalian TLRs recognize microbial infection or cell death–associated danger signals and trigger the appropriate cellular response. These responses determine strength outcome of host–microbe interaction. are transmembrane proteins located on plasma endosomal membrane. Their ectodomains specific endogenous ligands, cytoplasmic domains interact with to activate intracellular signaling pathways. TLR9, an TLR, is activated by endocytosed DNA. Activated TLR9 recruits adapter MyD88 other...

10.4049/jimmunol.1700691 article EN The Journal of Immunology 2018-04-01

Abstract A novel reaction between sulfate radical anion (SO4•-) and cyanuric acid (CA), a non-degradable end product of the oxidative degradation triazine based herbicide, atrazine, is presented using laser flash photolysis steady state radiolysis techniques at pH 5. second order rate constant 1.9×107 dm3 mol-1 s-1 has been determined transient intermediate (λmax=330 nm) assigned to cation CA (CA•+). The profile indicated that about 76% have decomposed after an absorbed γ-radiation dose 18...

10.1246/cl.2002.74 article EN Chemistry Letters 2002-01-01

ABSTRACT Many viruses activate cellular autophagy in infected cells to facilitate their replication. Recently, we identified an interferon (IFN)-stimulated gene (ISG) Tudor domain containing 7 (TDRD7), which inhibits viral replication by blocking pathway. Here, present a molecular mechanism for TDRD7 action and its relative contribution protection against pathogenesis. inhibited the activation of adenosine monophosphate (AMP)-activated protein kinase (AMPK), required initiating autophagy....

10.1128/mbio.00611-23 article EN cc-by mBio 2023-09-15

A study is made of the kinetics and mechanism reaction radiolytically produced hydrated electron (e-aq) with some triazine derivatives [1,3,5-triazine (T), 2,4,6-trimethoxy-1,3,5-triazine (TMT), 2,4-dioxohexahydro-1,3,5-triazine (DHT), 6-chloro N-ethyl N-(1-methylethyl)-1,3,5-triazine 2,4-diamine (atrazine, AT), cyanuric acid (CA)] in aqueous medium using pulse steady-state radiolysis techniques. The second-order rate constants were determined from pseudo first-order decay e-aq presence...

10.1021/jf061916d article EN Journal of Agricultural and Food Chemistry 2006-09-22

Pulse radiolysis and density functional theory (DFT) calculations at B3LYP/6-31+G(d,p) level have been carried out to probe the reaction of water-derived hydroxyl radicals (•OH) with 5-azacytosine (5Ac) 5-azacytidine (5Acyd) near neutral basic pH. A low percentage nitrogen-centered oxidizing radicals, a high non-oxidizing carbon-centered were identified based on transient intermediates 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonate), ABTS2-. Theoretical suggests that N3 atom in 5Ac is most...

10.1021/jp063958a article EN The Journal of Physical Chemistry A 2006-09-21

Pulse and steady state radiolysis techniques have been used to determine the bimolecular rate constants investigate spectral nature of intermediates degradation induced by hydroxyl radicals (•OH) with 1,3,5-triazine (T), 2,4,6-trimethoxy-1,3,5-triazine (TMT), 2,4-dioxohexahydro-1,3,5-triazine (DHT) in aqueous medium. A competitive kinetic method KSCN as •OH scavenger was for reaction T, TMT, DHT. The are 3.4 × 109, 2.06 108, 1.61 109 dm3 mol-1 s-1 respectively, DHT at pH ∼6. transient...

10.1021/jf991025o article EN Journal of Agricultural and Food Chemistry 2000-07-13

Reactions of hydroxyl radicals (•OH) with 2-amino-4-methyl pyrimidine (AMP), 2-amino-4,6-dimethyl (ADMP), 2-amino-4-methoxy-6-methyl (AMMP), 2-amino-4-hydroxy-6-methyl (AHMP), 4,6-dihydroxy-2-methyl (DHMP), 2,4-dimethyl-6-hydroxy (DMHP), 6-methyl uracil (MU), and 5,6-dimethyl (DMU) have been studied by pulse radiolysis steady-state techniques at different pH values. The second-order rate constants the reaction •OH these systems are order (2−9) × 109 dm3 mol-1 s-1 near neutral pH. difference...

10.1021/jp0117720 article EN The Journal of Physical Chemistry A 2002-02-26

S-Nitrosoglutathione (GSNO) undergoes decomposition induced by hydroxyl radicals (·OH) in aqueous medium at neutral pH forming nitrite (NO2−) and glutathione disulfide (GSSG) therefore it is proposed that ·OH could interfere the GSNO metabolism.

10.1039/b004706f article EN Chemical Communications 2000-01-01

Abstract Toll-like receptors (TLRs) are transmembrane proteins required for recognizing microbial components or cellular danger signals to activate intracellular signaling pathways leading induction of anti-microbial and inflammatory genes. Inactive TLRs require ligand-induced activation recruit adaptor proteins, e.g., MyD88, trigger the synthesis cytokines interferons. TLR9 is an endosomal membrane-bound protein, which binds CpG-containing DNA endogenous from dead cells tissue damage. We...

10.1101/2024.07.03.601759 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-07-05

The reaction of the hydroxyl radical (.OH) with S-nitroso derivatives cysteine, acetylcysteine and glutathione was studied at neutral acidic pH. second-order rate constants were determined by a competition kinetic method using deoxyribose-thiobarbituric acid assay. diffusion controlled 2.27, 1.94 1.46 x 10(10) dm3 mol-1 s-1, for S-nitrosocysteine, S-nitrosoacetylcysteine S-nitrosoglutathione respectively, major products degradation induced .OH found to be corresponding disulfide (-S-S-)...

10.1039/b212043g article EN Organic & Biomolecular Chemistry 2003-02-28
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