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Morya, V.

Publications and source records attributed to Morya, V..

3 recordsLinked to original sources

pH - responsive, reversible A-motif based DNA hydrogels: synthesis and biosensing applications

Functional DNA hydrogels using various motifs and functional groups require perfect sequence designing to avoid cross-bonding interference with self or other structural sequences. The present work reports an A-motif functional DNA hydrogel that does not require any sequence design. A-motif DNA is a non-canonical parallel DNA duplex structure comprises homopolymeric deoxyadenosines (poly-dA) strands that undergo conformational changes from single strands at neutral pH to a parallel duplex DNA helix at acidic pH. Despite many advantages over other DNA motifs like no sequence, design is required and no cross-bonding interference with other structural sequences, A-motif has not been explored much. We successfully synthesized DNA hydrogel utilizing A-motif as a reversible handle to polymerize DNA three-way junction (3WJ). The composed A-motif hydrogel was first characterized by EMSA, & DLS, which shows the formation of higher-order structures. Further, we utilized imaging techniques like atomic force microscopy (AFM) and scanning electron microscope (SEM) validating its hydrogel like highly branched morphology. pH-induced conformational transformation from monomers to gel is quick and reversible, and was analysed for multiple acid-base cycles. The sol-to-gel transitions and gelation properties is further examined using rheological studies. The use of A-motif hydrogel in the visual detection of pathogenic target nucleic acid sequence is demonstrated for the first time using the capillary assay. Moreover, the pH-induced hydrogel formation is observed in-situ as a layer over the mammalian cells. The proposed A-motif DNA scaffold has enormous potential in designing stimuli-responsive nanostructures that can be utilized for many biological applications.

bioengineering↗

Ligand geometry dictates cellular and in vivo uptake of 3D DNA nanostructures

Fabrication of nanoscale DNA devices to generate 3D nano-objects with precise control of shape, size, and presentation of ligands has shown tremendous potential for therapeutic applications. The interactions between different topologies of 3D DNA nanostructures and the cell membranes are crucial for designing efficient tools for interfacing DNA devices with biological systems. The practical applications of these DNA nanocages are still limited in cellular and biological systems owing to the limited understanding of interactions of different surface topologies of DNA nanodevices with cell membranes. The correlation between the geometry of DNA nanostructures and their internalization efficiency remains elusive. We investigated the influence of the shape and size of 3D DNA nanostructure on their cellular internalization efficiency. We found that of different geometries designed, one particular geometry, i.e., the tetrahedral shape, is more favoured over other geometries for their cellular uptake in 2D and 3D cell models. This is also replicable for cellular processes like 3D cell invasion assays in 3D spheroid models and passing the epithelial barriers in in-vivo zebrafish model systems. Our work establishes ground rules for the rational designing of DNA nanodevices for their upcoming biological and biomedical applications.

bioengineering↗

DESIGNER DNA HYDROGELS TO STIMULATE 3D CELL INVASION BY ENHANCED RECEPTOR EXPRESSION AND MEMBRANE ENDOCYTOSIS

DNA has emerged as one of the smartest biopolymers to bridge the gap between chemical science and biology to design scaffolds like hydrogels by physical entanglement or chemical bonding with remarkable properties. We present here a completely new application of DNA based hydrogels in terms of their capacity to stimulate membrane endocytosis, leading to enhanced cell spreading and invasion for cells in ex-vivo 3D spheroids models. Multiscale simulation studies along with DLS data showed that the hydrogel formation was enhanced at lower temperature and it converts to liquid with increase in temperature. DNA hydrogels induced cell spreading as observed by increase in cellular area by almost two-folds followed by increase in receptor expression, endocytosis and 3D invasion potential of migrating cells. Our first results lay the foundation for upcoming diverse applications of hydrogels to probe and program various cellular and physiological processes that can have lasting applications in stem cells programming and regenerative therapeutics.

bioengineering↗