In situ PKA activity assay by selective detection of its catalytic subunit using antibody arrays

2016 ◽  
Vol 11 (1) ◽  
pp. 57-66 ◽  
Author(s):  
Danishmalik Rafiq Sayyed ◽  
Se-Hui Jung ◽  
Min-Soo Kim ◽  
Eun-Taek Han ◽  
Won Sun Park ◽  
...  
2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Huilei Wang ◽  
Alan Poe ◽  
Lydia Pak ◽  
Kavitha Nandakumar ◽  
Sandeep Jandu ◽  
...  

2020 ◽  
Vol 8 (18) ◽  
pp. 9077-9084
Author(s):  
Qiong Wang ◽  
Lei Zhang
Keyword(s):  

A novel biomolecule-free PEC platform based on a CuCo2S4@CuCo2O4/CC integrated electrode for the selective detection of l-Cys.


2020 ◽  
Vol 37 (4) ◽  
pp. 189-198
Author(s):  
Muhamad Ramdzan Buyong ◽  
Farhad Larki ◽  
Celine Elie Caille ◽  
Norazreen Abd Aziz ◽  
Ahamad Ghadafi Ismail ◽  
...  

Purpose This paper aims to present the dielectrophoresis (DEP) force (FDEP), defined as microelectrofluidics mechanism capabilities in performing selective detection and rapid manipulation of blood components such as red blood cells (RBC) and platelets. The purpose of this investigation is to understand FDEP correlation to the variation of dynamic dielectric properties of cells under an applied voltage bias. Design/methodology/approach In this paper, tapered design DEP microelectrodes are used and explained. To perform the characterization and optimization by analysing the DEP polarization factor, the change in dynamic dielectric properties of blood components are observed according to the crossover frequency (fxo) and adjustment frequency (fadj) variation for selective detection and rapid manipulation. Findings Experimental observation of dynamic dielectric properties change shows clear correlation to DEP polarization factor when performing selective detection and rapid manipulation. These tapered DEP microelectrodes demonstrate an in situ DEP patterning efficiency more than 95%. Research limitations/implications The capabilities of tapered DEP microelectrode devices are introduced in this paper. However, they are not yet mature in medical research studies for various purposes such as identifying cells and bio-molecules for detection, isolation and manipulation application. This is because of biological property variations that require further DEP characterization and optimization. Practical implications The introduction of microelectrofluidics using DEP microelectrodes operate by selective detecting and rapid manipulating via lateral and vertical forces. This can be implemented on precision health-care development for lab-on-a-chip application in microfluidic diagnostic and prognostic devices. Originality/value This study introduces a new concept to understand the dynamic dielectric properties change. This is useful for rapid, label free and precise methods to conduct selective detection and rapid manipulation of mixtures of RBC and platelets. Further, potential applications that can be considered are for protein, toxin, cancer cell and bacteria detections and manipulation. Implementation of tapered DEP microelectrodes can be used based on the understanding of dynamic dielectric properties of polarization factor analysis.


2014 ◽  
Vol 87 ◽  
pp. 287-291 ◽  
Author(s):  
Lena Johansson ◽  
Eleanor Bakhshandeiar ◽  
Andy Pearce ◽  
Sean Collins ◽  
Pascal Orlandini ◽  
...  
Keyword(s):  

2017 ◽  
Vol 247 ◽  
pp. 681-690 ◽  
Author(s):  
Xinlei Cui ◽  
Yingming Xu ◽  
Xianfa Zhang ◽  
Xiaoli Cheng ◽  
Shan Gao ◽  
...  

2019 ◽  
Vol 33 (S1) ◽  
Author(s):  
Huilei Wang ◽  
Mahmoud Abouelkheir ◽  
Alan Poe ◽  
Yurie Hong ◽  
Sandeep Jandu ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Huilei Wang ◽  
Alan Poe ◽  
Lydia Pak ◽  
Sandeep Jandu ◽  
Kavitha Nandakumar ◽  
...  

AbstractThe lysyl oxidase family of enzymes (LOXs) catalyze oxidative deamination of lysine side chains on collagen and elastin to initialize cross-linking that is essential for the formation of the extracellular matrix (ECM). Elevated expression of LOXs is highly associated with diverse disease processes. To date, the inability to detect total LOX catalytic function in situ has limited the ability to fully elucidate the role of LOXs in pathobiological mechanisms. Using LOXL2 as a representative member of the LOX family, we developed an in situ activity assay by utilizing the strong reaction between hydrazide and aldehyde to label the LOX-catalyzed allysine (-CHO) residues with biotin-hydrazide. The biotinylated ECM proteins are then labeled via biotin-streptavidin interaction and detected by fluorescence microscopy. This assay detects the total LOX activity in situ for both overexpressed and endogenous LOXs in cells and tissue samples and can be used for studies of LOXs as therapeutic targets.


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