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An artificial intelligence program may enable the first simple production of customizable proteins called zinc fingers to treat diseases by turning genes on and off.

The researchers at NYU Grossman School of Medicine and the University of Toronto who designed the tool say it promises to accelerate the development of gene therapies on a large scale.

Illnesses including cystic fibrosis, Tay-Sachs disease, and are caused by errors in the order of DNA letters that encode the operating instructions for every human cell. Scientists can in some cases correct these mistakes with gene editing methods that rearrange these letters.

Last week, it was revealed that microplastics were found for the first time in fresh Antarctic snow. They were discovered high in the Alps, bottled water, and human blood.

They can be harmful to animals if ingested. But the growing menace is difficult to remove — considering their size — especially once they settle into nooks and crannies at the bottom of waterways.

Norovirus is sometimes referred to as the stomach flu, but it is not related to the influenza virus. Rather, it is a highly contagious virus that typically causes gastrointestinal symptoms like diarrhea, vomiting, nausea and stomach pain. Mild fever and aches are possible, too.

Just a few virus particles are enough to make someone sick, and they spread easily via hands, surfaces, food and water. An infected person can transmit the virus for days after they’re feeling better, potentially even up to two weeks, according to the CDC.

Regionally, the Midwest had the highest average test positivity rate for norovirus as of Saturday, at over 19% — higher than any other week in the last year.

Illustrated is the power of combined interference with different DNA damage response processes to combat cancer: Homologous recombination, which is selectively deficient in the tumour due to the BRCA defect, and base excision repair of single strand breaks, which is blocked by the administration of PARP inhibitors.

Client:
Dr. Rini de Crom.
Dr. Marja Miedema.
www.erasmusmc.nl, 2014

www.ddresponse.eu/

Funded by the 7th Framework Programme of the European Commission in the theme Health.

These animations show cellular biology on the molecular scale. The structure of chromatin, the processes of transcription, translation, DNA replication, and cell division are shown. All animations are scientifically accurate and derived from molecular biology and crystallography research. I have composed this video from multiple animations under fair use for non-profit, educational purposes. I do not claim copyright on this video or its contents, with the exception of the cell image. Most credit goes to Drew Berry and the Walter and Eliza Hall Institute of Medical Research (WEHI TV) for the animations. Full credits are at the end of the video.

An exploration of the structure of deoxyribonucleic acid, or DNA. If you want to learn more, join our free MITx #700x Introduction to Biology course (http://bit.ly/700xBio) or our #703x Genetics (https://bit.ly/GeneticsPart1) Also try #705x Biochemistry. (http://bit.ly/705xBiochem) or our advanced #728x Molecular Biology course (http://bit.ly/MITx7281x). Learn more about our work: http://web.mit.edu/mitxbio/courses.html.

This video was created for MITx 7.28.1x Molecular Biology: DNA Replication & Repair, offered on edX.

Created by Betsy Skrip (http://betsyskrip.com) and Sera Thornton (http://serathornton.com), with special thanks to Mary Ellen Wiltrout, Stephen Bell, Ceri Riley, and Julian Samal.

© 2015 Massachusetts Institute of Technology. All rights reserved.

These are the molecular machines inside your body that make cell division possible. Animation by Drew Berry at the Walter and Eliza Hall Institute of Medical Research. http://wehi.tv.

Special thanks to Patreon supporters:
Joshua Abenir, Tony Fadell, Donal Botkin, Jeff Straathof, Zach Mueller, Ron Neal, Nathan Hansen.

Support Veritasium on Patreon: http://ve42.co/patreon.

Every day in an adult human roughly 50–70 billion of your cells die. They may be damaged, stressed, or just plain old — this is normal, in fact it’s called programmed cell death.

In this video students of the Maastricht Science Program NanoBiology Course 2020, show their explanation of the SARS-CoV-2 viral budding. Using CellPAINT, UCFS Chimera and their creativity they explain the nanobiology of how the SARS-CoV-2 virion can bud and leave the cell.

Viruses are not living things. They are just complicated assemblies of molecules, in particular macromolecules such as proteins, oligonucleotides, combined with lipids and carbohydrates. A virus cannot function or reproduce by itself. It needs a host cell.

When a virus enters the host cell, a series of chemical reactions occur that lead to the production of new viruses. A virus needs to find a host cell, attach to it, enter it, and reprogram it such that it will replicate its genome and produce new proteins that allow the assembly of a new virus. Once new viruses have been assembled, they need to get out of the original host cell, on their way to the next host cell they can exhaust. Some viruses have an easy way out: they use up all the resource of the host cells until it dies and lyse. This would only work for naked viruses such as polyomavirus and adenovirus, which lacks a lipid membrane.

Washing hands has been a standard measure since the start of this COVID-19 pandemic. The soap will disintegrate the lipid envelop of the SARS-CoV2 viral particles, as this is an enveloped virus. Enveloped viruses need envelopment, a process in which the capsids become surrounded by a lipid bilayer. This process takes place prior to release. Two mechanisms for envelopment exist. First, envelopment can proceed sequentially after the completion of capsid assembly. The fully assembled capsids are recruited to the membrane by interaction of the viral capsids with viral envelope glycoprotein. Examples of this include herpesvirus and hepatitis B virus. Secondly, the envelopment can occur simultaneously with the capsid assembly. Retrovirus is the representative of this coupled mechanism.