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Related Concept Videos

Nucleic Acids02:43

Nucleic Acids

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Nucleic acids are the most important macromolecules for the continuity of life. They carry the cell's genetic blueprint and carry instructions for its functioning.
DNA and RNA
The two main types of nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). DNA is the genetic material in all living organisms, ranging from single-celled bacteria to multicellular mammals. It is in the nucleus of eukaryotes and in the organelles, chloroplasts, and mitochondria. In prokaryotes,...
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Nucleic acids02:43

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Nucleic acids are the most important macromolecules for the continuity of life. They carry the cell's genetic blueprint and carry instructions for its functioning.
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Nucleic Acid Structure01:25

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The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
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Nucleic Acids and Nucleotides01:20

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Nucleic acids are the most important macromolecules for the continuity of life. They carry the cell's genetic blueprint and have instructions for its functioning. The two main types of nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
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Biosynthesis of Nucleic Acids01:28

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Nucleic acid biosynthesis is a fundamental biochemical process that produces the purine and pyrimidine nucleotides essential for DNA and RNA synthesis. This pathway maintains a balanced nucleotide pool, preventing imbalances that could jeopardize genetic integrity and cellular function. Given the crucial role of nucleotides, their synthesis is tightly regulated to ensure proper cellular homeostasis.Purine BiosynthesisThe biosynthesis of purine nucleotides begins with ribose-5-phosphate, a...
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Correction: Kang et al. Fluid Flow to Electricity: Capturing Flow-Induced Vibrations with Micro-Electromechanical-System-Based Piezoelectric Energy Harvester. <i>Micromachines</i> 2024, <i>15</i>, 581.

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On-chip Isotachophoresis for Separation of Ions and Purification of Nucleic Acids
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Rapid Nucleic Acid Extraction and Purification Using a Miniature Ultrasonic Technique.

Darren W Branch1, Erika C Vreeland2, Jamie L McClain3

  • 1Nano and Micro Sensors Department, Sandia National Laboratories, Albuquerque, NM 87185, USA. dwbranc@sandia.gov.

Micromachines
|November 8, 2018
PubMed
Summary
This summary is machine-generated.

Miniature ultrasonic lysis rapidly extracts nucleic acids and proteins using acoustic waves. This novel system enhances lysis efficiency and DNA purification, offering a faster, chemical-free sample preparation method.

Keywords:
Point-of-Careacoustic lysisextractionmicrofluidicnucleic acidspurificationseparation

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Area of Science:

  • Biotechnology
  • Microfluidics
  • Biomedical Engineering

Background:

  • Traditional biological sample preparation methods for nucleic acid and protein extraction can be time-consuming and may involve harsh chemicals that interfere with downstream assays.
  • Acoustic lysis offers a rapid, chemical-free alternative for efficient cell membrane disruption.

Purpose of the Study:

  • To present a miniature acoustic nucleic acid extraction system utilizing a bulk acoustic wave (BAW) transducer array.
  • To evaluate the lysis effectiveness and optimize parameters like input power, energy dose, and flow rate.
  • To demonstrate on-chip DNA purification using various methods within microfluidic cartridges.

Main Methods:

  • Development of a miniature BAW transducer array using 36° Y-cut lithium niobate.
  • Integration of the BAW transducer with disposable laminate-based microfluidic cartridges.
  • Assessment of lysis effectiveness via adenosine triphosphate (ATP) release and cell viability measurements.
  • On-chip DNA purification using silica-based sol-gel, magnetic beads, and Nafion-coated electrodes.

Main Results:

  • The miniature BAW array demonstrated a 2.2× greater lysis dose (ATP released per joule) and 6.1× higher ATP release compared to a bench-top acoustic lysis system using E. coli.
  • An electric field-based nucleic acid purification method using Nafion films achieved 69.2% extraction efficiency in 10 minutes for 50 µL samples.
  • Established relationships between input power, energy dose, flow rate, and lysis efficiency.

Conclusions:

  • The miniature acoustic lysis system provides a highly efficient and rapid method for biological sample preparation.
  • On-chip DNA purification strategies integrated within the microfluidic cartridges are effective.
  • This technology holds promise for advancing rapid, point-of-care molecular diagnostics and sample preparation.