11 research outputs found
A Design of Digital Microfluidic Biochip along with Structural and Behavioural Features in Triangular Electrode Based Array
AbstractDigital microfluidic based biochip manoeuvres on the theory of microfluidic technology, having a broad variety of applications in chemistry, biology, environmental monitoring, military etc. Being concerned about the technological advancement in this domain, we have focused on equilateral triangular electrodes based DMFB systems. Accepting the associated design issues, here, we have addressed many facets of such electrodes regarding their structural and behavioural issues in comparison to the existing square electrodes. As the requisite voltage reduction is a key challenging design issues, to implement all the tasks using triangular electrodes that are possible in square electrode arrays as well, is a tedious job. Furthermore, to deal with this new design deploying triangular electrodes, we have analyzed all the necessary decisive factors including fluidic constraints to ensure safe droplet movements and other modular operations together with mixing and routing. Moreover, an algorithm has been developed to find a route for a given source and destination pair in this newly designed DMFB. Finally, we have included a comparative study between this new design and the existing one while encountering the above mentioned issues
Analysis of Free and Bound NADPH in Aqueous Extract of Human placenta Used as Wound Healer.
NADPH is an important biomolecule involved in cellular regeneration. The distribution of free and bound
NADPH in aqueous extract of human placenta used as a potent wound healer has been analyzed. Quantification
from fluorescence and immuno-affinity chromatography indicates that 75.1±2.2% of NADPH
present in the extract exists as free nucleotide or bound to very small peptides or amino acids whereas
the rest remains bound to large peptides. Inability to dissociate the bound form of the nucleotide from
the large peptides using urea or guanidium hydrochloride indicates that the binding is covalent. Identification
of a fragmented mass of m/z 382.94 (nicotinamide + sugar + phosphate) from the NADPH-peptide
conjugates supported the intactness of the nicotinamide moiety. Glutathione reductase assay indicated
that 95.2±3.5% of the total NADPH pool of the extract can act as cosubstrate of the enzyme. This indicates
that while a major fraction of free NADPH of the extract is easily available for cellular processes, the rest
can also function locally where the conjugated peptides are deposited
In vitro induction of nitric oxide by mouse peritoneal macrophages treated with human placental extract
Nitric oxide (NO) is an important cellular mediator of tissue repair. It is produced in macrophages by the enzyme inducible nitric oxide synthase (iNOS) during wound healing. An aqueous extract of human placenta used as wound healer, has been investigated in terms of induction of NO by mouse peritoneal macrophages as well as human monocyte derived macrophages. NO production was estimated in macrophages culture supernatants. Incubation of 0.1 to 20 mg/ml of placental extract with 2 Ă 106 cells in vitro produced 10 to 100 μ M of nitrite (n = 4) in a dose dependent manner suggesting production of NO. With increase of NO production, NADPH present in the applied extract decreased proportionately. Application of L-NG monomethyl arginine (L-NMMA), an NO synthase (NOS) inhibitor, reduced the production of NO at the basal level. Dose dependent release of IFN-Îł with respect to placental extract by the mouse macrophages was observed. It has been observed that human monocytes derived macrophages also produced significant amount of NO by induction of the extract. Similar induction of NO by placental extract in presence and absence of polymyxin B suggested that this property is not likely to be mediated by the endotoxin/LPS
Ubiquitin-Like Protein from Human Placental Extract Exhibits Collagenase Activity
<div><p>An aqueous extract of human placenta exhibits strong gelatinase/collagenase activity in zymography. 2-D gel electrophoresis of the extract with gelatin zymography in the second dimension displayed a single spot, identified as ubiquitin-like component upon MALDI/TOF MS/MS analysis. Immunoblot indicated presence of ubiquitin and absence of collagenase in the extract. Collagenase activity of the ubiquitin-like component was confirmed from the change in solubility of collagen in aqueous buffer, degradation of collagen by size-exclusion HPLC and atomic force microscopy. Quantification with DQ-gelatin showed that the extract contains 0.04 U/ml of collagenase activity that was inhibited up to 95% by ubiquitin antibody. Ubiquitin from bovine erythrocytes demonstrated mild collagenase activity. Bioinformatics studies suggest that placental ubiquitin and collagenase follow structurally divergent evolution. This thermostable intrinsic collagenase activity of placental extract might have wide physiological relevance in degrading and remodeling collagen as it is used as a drug for wound healing and pelvic inflammatory diseases.</p> </div
Identification of the component responsible for collagenase activity.
<p>(A) 2-D gel electrophoresis of placental extract (100x). Positions of Mw markers are indicated. (B) Gelatin zymography in the second dimension. The activity corresponded to spot number 3 of A. (C) Immunological cross-reactivity between anti-sera of ubiquitin and (a) ubiquitin, (b) peptide fraction and (c) ovalbumin. (D) Immunological cross-reactivity between anti-sera of peptide fraction and (a) collagenase, (b) peptide fraction and (c) ovalbumin. (E) Gelatin zymography. Lane 1, ubiquitin (bovine); and Lane 2, peptide fraction. The arrow indicates the faint band of ubiquitin which roughly corresponds to that of placental ubiquitin. (F) Silver stained SDS-PAGE of ubiquitin (bovine, lane 1) and peptide fraction (lane 2). Approximate Mw of ubiquitin bands have been indicated.</p
AFM of collagen.
<p>(A) Enlarged 3D view of collagen monomer filament (diameter 82±10 nm). (Lower Panel) Cross-section indicating intact collagen filament. (B) Amplitude flattened image of collagen (67.7 nm) incubated with collagenase. A fiber (7 nm) appearing from its side is also apparent. The bulge diameter of 32 nm is similar to another bulge (âŒ28.7 nm). (Lower Panel) Loss in integrity of collagen. The arrow on the left indicates the 7 nm fiber while that on the right indicates the 67.7 nm fiber. (C) Amplitude flattened image of collagen incubated with peptide fraction indicated two fragments of lengths 598 and 475 nm and width 59.6 nm each. (Lower Panel) Loss in integrity and fragmentation of collagen. (D) Topograph flattened image of collagen treated with ubiquitin indicates a single particle with a bulging head; scattered bulges are also apparent. (Lower Panel) Loss in integrity of collagen. The arrow indicates poor peak shape of the collagen and the possible region of wearing out from this molecule. In all the figures presented, a color scale bar indicating sample height from the mica sheet has been represented. The dark shade indicates depression of the sample while the white color represents maximum elevation.</p
Comparison between ubiquitin and collagenase.
<p>(A) 2.0.12 ClustalW Sequence alignment between human ubiquitin and 1C3TA (mutant ubiquitin). The â*â and â:âindicates identical and highly similar residues respectively. The mutated sequences have been highlighted in bold-red, which are also highly similar to corresponding ubiquitin amino acid residues. (B) Multiple sequence alignment of the peptidase domains of the matrix metalloproteases, obtained from their corresponding crystal structures, with 1C3TA by MAFFT (71) shows conservation of E<sub>51</sub> in 1C3TA with the catalytic E of the MMPs. The sequences have been represented as the MMP family_PDB ID. (C) Structural superimposition of the 3D-coordinates of the peptidase domain with the crystal structure of 1C3TA (I). Superimposition of 1AYK, of MMP1, peptidase domain (green) with 1C3TA (cyan). Panel II. Superimposition of 1A85, of MMP8, peptidase domain (green) with 1C3TA (cyan). Panel III. Superimposition of 1EUB, of MMP13, peptidase domain (green) on 1C3TA (cyan).</p
Gelatinase/Collagenase activity of Placental Extract.
<p>(A) Gelatin Zymography - Lane 1, MMP 2; lanes 2, 4 and 6, MMP 2 activation profile in presence of APMA for 0, 1 and 2 hrs; lanes 3, 5 and7, MMP 2 incubated with peptide fraction at 37°C for same duration. (B) Gelatin Zymography - Lane 1 and 2, 0.1 ng collagenase incubated at pH 7.5 for 0 and 20 h at 37°C; lanes 3 and 4, 20 ”g peptide fraction with 0.1 ng bacterial collagenase incubated for 0 and 20 h. (C) Collagen zymography. Lanes 1 and 2, 1.0 and 0.1 ng of collagenase; Lane 3, 20 ”g of placental peptide fraction. (D) SE-HPLC analysis of collagenase activity of placental extract. a: collagen (R<sub>t</sub>â=â9.66±0.05 min, nâ=â5), b: placental extract (15.46±0.08 min), c : collagen treated with the extract at 0 h (major components at 7.3±0.03 and 16.1±0.08 min) and d : 168 h (major components at 7.56±0.01, 8.20±0.03, 8.83±0.001 and 9.60±0.04 min) respectively (nâ=â5).</p