Enzyme Technologies 2013
DOI: 10.1002/9781118739907.ch1
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Assay Technologies for Proteases

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Cited by 3 publications
(2 citation statements)
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References 138 publications
(264 reference statements)
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“…Fluorimetric MMP peptides have been previously used to measure and quantify MMP activities from dentin and oral bacteria as they have higher sensitivity than colorimetric assays [15,17,35]. In the current study, human neutrophils showed activity towards the MMP substrates, and the activities either remained constant or became elevated throughout the 48 hours replacement cycle, suggesting their potential ability to degrade the collagen type I in tooth dentin.…”
Section: Mmp Activities From Neutrophilsmentioning
confidence: 57%
“…Fluorimetric MMP peptides have been previously used to measure and quantify MMP activities from dentin and oral bacteria as they have higher sensitivity than colorimetric assays [15,17,35]. In the current study, human neutrophils showed activity towards the MMP substrates, and the activities either remained constant or became elevated throughout the 48 hours replacement cycle, suggesting their potential ability to degrade the collagen type I in tooth dentin.…”
Section: Mmp Activities From Neutrophilsmentioning
confidence: 57%
“…From these energy predictions, it is reasonable to infer that the exothermic energy gained from Spike binding to TMPRSS2, MSP, and PSP may, in all three cases, provide ample energetic impetus for the enzyme to overcome the reactive barrier and cleave the peptide. While the precise reaction kinetics have not been reported for proteolytic cleavage by MSP and PSP, it is worth noting that widespread conservation of protease catalytic triad structures imposes homogeneity on reactive proficiency across the broad manifold of serine proteases [229][230][231]. Known proteolysis barriers for HIV protease (15.1-17.9 kcal/mol) [232,233], for example, bear a strong resemblance to TMPRSS2 reactive barriers.…”
Section: Prospective Biochemical Rationalizationsmentioning
confidence: 99%