2019
DOI: 10.1021/acs.analchem.9b01662
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Inhibitory Covalent Labeling and Clickable-Eu-Tagging-Based ICPMS: Measurement of pH-Dependent Absolute Activities of the Cathepsins in Hepatocyte Lysosomes

Abstract: We report an inhibitory covalent labeling and clickable-element-tagging strategy for measuring the absolute activity of a protease in cells using inductively coupled plasma mass spectrometry (ICPMS). Epoxysuccinyl-leucine-tyrosine-6-aminocaproic-lysine-amino-Boc-alkyne (epoxysuccinyl-LYK-alkyne) was designed and synthesized to achieve irreversibly labeling of the cysteine cathepsins, recording their momentary activities. L and Y assisted epoxysuccinyl-LYK-alkyne in accessing the deprotonated −S − of Cys25, loc… Show more

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Cited by 15 publications
(10 citation statements)
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“…Atomic spectrometry (AS) (atomic absorption spectrometry, atomic emission spectrometry, and atomic fluorescence spectrometry (AFS)) and inductively coupled plasma mass spectrometer (ICP-MS) have been widely applied in environmental monitoring, food safety testing, and other industries. , In view of the many advantages of AS and the need for precise detection methods in biomedicine, AS has been widely used in bioassay. Within this field, Zhang et al pioneered the ICP-MS-based bioassay for a sensitive and accurate determination of proteins using antibodies as recognition probes. , Subsequently, researchers introduced biorecognition probes such as nucleic acid aptamers and peptides into AS, and developed various biomolecule detection methods, which greatly expanded the application of AS in bioanalysis. , Although these AS bioassay methods hold the advantages of high sensitivity, good specificity, and accuracy, labeling and signal molecule separation are still required, which adds complexity and thus puts them at a disadvantage …”
Section: Introductionmentioning
confidence: 99%
“…Atomic spectrometry (AS) (atomic absorption spectrometry, atomic emission spectrometry, and atomic fluorescence spectrometry (AFS)) and inductively coupled plasma mass spectrometer (ICP-MS) have been widely applied in environmental monitoring, food safety testing, and other industries. , In view of the many advantages of AS and the need for precise detection methods in biomedicine, AS has been widely used in bioassay. Within this field, Zhang et al pioneered the ICP-MS-based bioassay for a sensitive and accurate determination of proteins using antibodies as recognition probes. , Subsequently, researchers introduced biorecognition probes such as nucleic acid aptamers and peptides into AS, and developed various biomolecule detection methods, which greatly expanded the application of AS in bioanalysis. , Although these AS bioassay methods hold the advantages of high sensitivity, good specificity, and accuracy, labeling and signal molecule separation are still required, which adds complexity and thus puts them at a disadvantage …”
Section: Introductionmentioning
confidence: 99%
“…A multiplex and accurate technique for biomolecule quantification plays an important role in the elucidation of molecular mechanisms and early diagnosis for many diseases because living bodies are complicated assemblies of multiple biomolecules that interact with each other to achieve different physiological states. Complementary to the mainstream fluorescent tagging that is often limited by molecular spectral overlapping, metal stable isotope tagging has demonstrated great and unique success in the multiplex and accurate quantification of proteins, enzymes, , small molecules, nucleic acids, and single cells, thanks to the excellent mass spectral resolution, wide dynamic ranges of 9 orders of magnitude, low matrix effect, and high metrological value for absolute quantification. For instance, Nolan et al simultaneously detected 34 parameters in single cells using polymer lanthanide isotopes as tags, and the assay provided a systematic view of the immune signal in human hematopoietic cells . Zhang et al.…”
mentioning
confidence: 99%
“…Epoxysuccinyl-leucine-tyrosine (Epo-LeuTyr) derivatives have been widely used to covalently modify the active site cysteine of cathepsins. ,, To fluorescently label cathepsins, we first prepared Epo-LeuTyr with C-terminal coumarin (Epo-LeuTyr-CM). Cells staining with Epo-LeuTyr-CM exhibited poor fluorescence in lysosomes, reflecting poor targeting of the substrate for lysosomes (Figure S1).…”
Section: Resultsmentioning
confidence: 99%