scholarly journals Synthesis and characterization of TEMPO-oxidized peptide-cellulose conjugate biosensors for detecting human neutrophil elastase

Cellulose ◽  
2022 ◽  
Author(s):  
Robert T. Mackin ◽  
Krystal R. Fontenot ◽  
J. Vincent Edwards ◽  
Nicolette T. Prevost ◽  
Casey Grimm ◽  
...  

AbstractHere we describe the synthesis and characterization of a peptide-cellulose conjugate biosensor based on TEMPO-oxidized nanofibrillated cellulose (tNFC) for detecting elevated levels of human neutrophil elastase (HNE) in chronic wounds. The fluorescent peptide HNE substrate constructed from n-succinyl-Ala-Pro-Ala-7-amino-4-methyl-coumarin was attached to the TEMPO-oxidized cellulose surface via polyethylene glycol linker. The characterization of the biosensor conjugate shows a high degree of peptide incorporation onto the surface with the degree of substitution of 0.057. The relatively small crystallite size of 26.0 Å compared to other cellulose- and nanocellulose-based materials leads to a large specific surface area which can promote access of HNE to the enzyme substrates due to decreased steric interactions. Likewise, the porosity for tNFC was found to be higher than all other samples, including the nanocellulosic aerogel, lending to its hydrogel-like nature. The properties of tNFC were compared to other cellulose-based materials. The volume of each crystallite and volume ratio to the largest sample was calculated. tNFC was found to occupy the smallest space resulting in high amounts of sensors per crystallite unit volume. With a small crystallite volume and large number of sensors, the tNFC peptide-cellulose conjugate biosensor could provide a more sensitive system and is a good candidate for point of care diagnostic devices for detecting elevated protease levels in humans.

Cellulose ◽  
2016 ◽  
Vol 23 (2) ◽  
pp. 1283-1295 ◽  
Author(s):  
J. Vincent Edwards ◽  
Krystal R. Fontenot ◽  
David Haldane ◽  
Nicolette T. Prevost ◽  
Brian D. Condon ◽  
...  

Cellulose ◽  
2016 ◽  
Vol 23 (2) ◽  
pp. 1297-1309 ◽  
Author(s):  
Krystal R. Fontenot ◽  
J. Vincent Edwards ◽  
David Haldane ◽  
Elena Graves ◽  
Michael Santiago Citron ◽  
...  

1991 ◽  
Vol 144 (4) ◽  
pp. 875-883 ◽  
Author(s):  
Joseph C. Williams ◽  
Ronald C. Falcone ◽  
Cathy Knee ◽  
Ross L. Stein ◽  
Anne M. Strimpler ◽  
...  

1994 ◽  
Vol 300 (2) ◽  
pp. 401-406 ◽  
Author(s):  
A Dubin ◽  
J Potempa ◽  
J Travis

In order better to understand the pathophysiology of the equine form of emphysema, two elastinolytic enzymes from horse neutrophils, referred to as proteinases 2A and 2B, have been extensively characterized and compared with the human neutrophil proteinases, proteinase-3 and elastase. Specificity studies using both the oxidized insulin B-chain and synthetic peptides revealed that cleavage of peptide bonds with P1 alanine or valine residues was preferred. Further characterization of the two horse elastases by N-terminal sequence and reactive-site analyses indicated that proteinases 2A and 2B have considerable sequence similarity to each other, to proteinase-3 from human neutrophils (proteinase 2A), to human neutrophil elastase (proteinase 2B) and to a lesser extent to pig pancreatic elastase. Horse and human elastases differed somewhat in their interaction with some natural protein proteinase inhibitors. For example, in contrast with its action on human neutrophil elastase, aprotinin did not inhibit either of the horse proteinases. However, the Val15, alpha-aminobutyric acid-15 (Abu15), alpha-aminovaleric acid-15 (Nva15) and Ala15 reactive-site variants of aprotinin were good inhibitors of proteinase 2B (Ki < 10(-9) M) but only weak inhibitors of proteinase 2A (Ki > 10(-7) M). In summary, despite these differences, the horse neutrophil elastases were found to resemble closely their human counterparts, thus implicating them in the pathological degradation of connective tissue in chronic lung diseases in the equine species.


2017 ◽  
Vol 11 (1) ◽  
Author(s):  
Letizia Crocetti ◽  
Gianluca Bartolucci ◽  
Agostino Cilibrizzi ◽  
Maria Paola Giovannoni ◽  
Gabriella Guerrini ◽  
...  

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