Related Experiment Video
Updated: Feb 12, 2026

12:03
Protocols for C-Brick DNA Standard Assembly Using Cpf1
Published on: June 15, 2017
8.7K
Vesicle Tubulation with Self-Assembling DNA Nanosprings
Michael W Grome1, Zhao Zhang1, Frédéric Pincet1,2
1Department of Cell Biology & Nanobiology Institute, Yale University, 850 West Campus Drive, West Haven, CT, 06516, USA.
Angewandte Chemie (International Ed. in English)
|March 26, 2018
Summary
Researchers created DNA nanosprings to deform cell membranes, mimicking natural proteins. This self-assembly method avoids harsh chemicals for creating membrane tubules, offering a new tool in nanotechnology.
Area of Science:
- Nanotechnology
- Bioengineering
- Biophysics
Background:
- Developing artificial nanomachines to control membrane curvature is a key goal in nanotechnology and bioengineering.
- Natural membrane-deforming proteins serve as inspiration for creating such artificial systems.
Purpose of the Study:
- To design and demonstrate DNA-origami curls that polymerize into nanosprings for inducing specific membrane curvatures.
- To investigate the efficacy of these DNA nanosprings in deforming biological vesicles.
Main Methods:
- Design of DNA-origami structures capable of self-assembly into nanosprings.
- Application of DNA nanosprings to lipid vesicles to induce membrane deformation.
- Observation of membrane tubule formation mediated by DNA self-assembly.
Main Results:
- DNA-origami curls successfully polymerized into nanosprings, demonstrating their ability to deform vesicles.
- Emergence of DNA-coated membrane tubules from spherical vesicles upon DNA-origami polymerization or high surface coverage.
- Successful membrane tubulation without the use of detergents or complex top-down manipulation, highlighting a self-assembly approach.
Conclusions:
- DNA self-assembly offers a novel, detergent-free method for creating membrane tubules and controlling membrane curvature.
- The design of DNA-origami structures and the conditions of deformation significantly impact tubulation efficiency and morphology.
- This work highlights the complex interactions between lipid bilayers and DNA structures for nanoscale engineering applications.
Related Concept Videos
Renal Tubule and Collecting Duct
3.6K
The renal tubule is divided into three parts: the proximal convoluted tubule (PCT), the Loop of Henle (LOH), and the distal convoluted tubule (DCT).
Proximal Convoluted Tubule (PCT):
The PCT is the initial segment of the renal tubule, extending from the Bowman's capsule that encloses the glomerulus. Its convoluted structure and microvilli-lined cells increase the surface area for reabsorption. The PCT reabsorbs glucose, amino acids, sodium, and water from the filtrate, ensuring essential...
Proximal Convoluted Tubule (PCT):
The PCT is the initial segment of the renal tubule, extending from the Bowman's capsule that encloses the glomerulus. Its convoluted structure and microvilli-lined cells increase the surface area for reabsorption. The PCT reabsorbs glucose, amino acids, sodium, and water from the filtrate, ensuring essential...
3.6K
From DNA to Protein
22.6K
The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
22.6K
Protein Complex Assembly
16.9K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types. Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Many viruses self-assemble into a fully functional unit using the infected host cell to...
16.9K
Spindle Assembly
4.3K
Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
4.3K
Oligosaccharide Assembly
3.7K
Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
Multiple sugar molecules that may or may...
Multiple sugar molecules that may or may...
3.7K
DNA Topoisomerases
35.8K
Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
35.8K

