The previously demonstrated nonintrusive time-of-flight molecular velocity tagging method, hydroxyl tagging velocimetry (HTV), has shown the capability of operating both at room temperature and in flames. Well-characterized jets of either air (nonreacting cases) or hydrogen-air diffusion flames (reacting cases) are employed. A 7 x 7 OH line grid is generated first through the single-photon photodissociation of H2O by a approximately 193 nm pulsed narrowband ArF excimer laser and is subsequently revealed by a read laser sheet through fluorescence caused by A2sigma+(v' = 3) <-- X2pi(i)(v'' = 0), A2sigma+(v' = 1) <-- X2pi(i)(v'' = 0), or A2sigma+(v' = 0) < or = X2pi(i)(v'' = 0) pumping at approximately 248, approximately 282, or approximately 308 nm, respectively. A detailed discussion of the spectroscopy and relative signal intensity of these various read techniques is presented, and the implications for optimal HTV performance are discussed.
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http://dx.doi.org/10.1364/ao.44.006616 | DOI Listing |
Prolyl Hydroxylase Domain protein 2 (PHD2) targets Hypoxia Inducible Factor alpha subunits (HIFα) for oxygen-dependent proline hydroxylation that leads to subsequent ubiquitination and degradation of HIFα. In addition to HIF proteins, growing evidence suggested that PHD2 may exert its multifaceted function through hydroxylase-dependent or independent activities. Given the critical role of PHD2 in diverse biological processes, it is important to comprehensively identify potential PHD2 interacting proteins.
View Article and Find Full Text PDFPhysiol Mol Biol Plants
December 2024
Department of Fruit Science, College of Horticulture and Forestry, CAU (I), Pasighat, Arunachal Pradesh 791102 India.
An experiment was performed to understand the effects of aluminium toxicity (AlCl·6HO) on Kachai lemon growth and development. The toxic effects of aluminium were assessed for 45 days in sand media. With untreated pots serving as the control, seedlings of 1 month old were exposed to three concentrations of AlCl·6HO: 300 μM, 600 μM and 900 μM.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, U.K.
The catalytic competency of the ribosome in extant protein biosynthesis is thought to arise primarily from two sources: an ability to precisely juxtapose the termini of two key substrates─3'-aminoacyl and -acyl-aminoacyl tRNAs─and an ability to ease direct transpeptidation by their desolvation and encapsulation. In the absence of ribosomal, or enzymatic, protection, however, these activated alkyl esters undergo efficient hydrolysis, while significant entropic barriers serve to hamper their intermolecular cross-aminolysis in bulk water. Given that the spontaneous emergence of a catalyst of comparable size and sophistication to the ribosome in a prebiotic RNA world would appear implausible, it is thus natural to ask how appreciable peptide formation could have occurred with such substrates in bulk water without the aid of advanced ribozymatic catalysis.
View Article and Find Full Text PDFChemistry
December 2024
Key Laboratory of Advanced Mass Spectrometry and Molecular Analysis of Zhejiang Province, Institute of Mass Spectrometry, School of Material Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
A hydroxyl-tagged porous aromatic framework PAF-NBU2-OH was task-specifically designed and successfully synthesized targeted toward immobilizing chiral catalysts. Using proline-type compound as model chiral organocatalyst, PAF-NBU2-OH was used as a platform to covalently link proline-type group. The obtained PAF-immobilized organocatalyst PAF-NBU2-OPro featured high chemical stability in different solvents even under very harsh conditions.
View Article and Find Full Text PDFAnal Chem
October 2024
MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing 100084, China.
Circulating neutral glycosphingolipids (neutral GSLs (nGSLs)) are a unique subset of nGSLs that detach from organs or cell membranes and enter the bloodstream. Altered molecular distribution of circulating nGSL is increasingly associated with diseases. However, profiling of circulating nGSLs presents a lasting challenge due to their low abundances and structural complexity.
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