Skip to content
0:00 / 0:00

Ron Vale (UCSF, HHMI) 1: Molecular Motor Proteins

Science Communication Lab

194K subscribers • 2 videos on Rounds

YouTube
  • Recommended by 3 people, in Hacker News, across 3 different months.
  • Presented by Ron Vale, as the video describes them

Assumes interest and some biology. Education, not medical advice.

942K views10 years ago3 recommendations

How the body worksCells and moleculesPhysiology

Ron Vale explains how molecular motor proteins like kinesin, dynein, and myosin convert chemical energy into movement within cells.

ibiology.org/cell-biology/motor-proteins/ Molecular motor proteins are fascinating enzymes that power much of the movement performed by living organisms. In this introductory lecture, I will provide an overview of the motors that move along cytoskeletal tracks (kinesin and dynein which move along microtubules and myosin which moves along actin). The talk first describes the broad spectrum of biological roles that kinesin, dynein and myosin play in cells. The talk then discusses how these nanoscale proteins convert energy from ATP hydrolysis into unidirectional motion and force production, and compares common principles of kinesin and myosin. The talk concludes by discussing the role of motor proteins in disease and how drugs that modulate motor protein activity can treat human disease. Part 2 discusses recent work from the Vale laboratory and other groups, on the mechanism of movement by dynein, a microtubule motor that is less well understood than kinesin and myosin. The lecture discusses the unusual properties of dynein stepping along microtubules, which have been uncovered using single molecule techniques. The nucleotide-driven structural changes in the dynein motor domain (elucidated by X-ray crystallography and electron microscopy) are also described. A model for dynein movement in the form of an animation is presented. However, much remains to be done in order to understand how this motor works and to test which elements of this model are correct. The third (last) part of the lecture explains how the movement of mammalian dynein is regulated by other proteins such dynactin and adapter proteins. It also describes the effect of post-translational modifications of tubulin on dynein motility. This talk features the use of single molecule imaging techniques and biochemical reconstitution to study these problems. Unanswered questions on dynein regulation are also presented. Speaker Biography: Ron Vale is a Professor of Cellular and Molecular Pharmacology at the University of California, San Francisco and an Investigator of the Howard Hughes Medical Institute. He is also the founder of the iBiology project. Vale received a B.A. degree in biology and chemistry from the University of California, Santa Barbara, and a Ph.D. degree in neuroscience from Stanford University. His graduate and postdoctoral studies at the Marine Biological Laboratory led to the discovery of kinesin, a microtubule-based motor protein. Dr. Vale’s honors include the Pfizer Award in enzyme chemistry, the Lasker Award for Basic Medical Research, and elections to the National Academy of Sciences, National Academy of Medicine, and the American Academy of Arts and Sciences. Besides studying the mechanism of motor proteins, Vale’s laboratory studies mitosis, RNA biology, and the mechanism of T cell signaling.

Why it's here

3 people recommend this, 1 disputes it

What people say. Recommended as a fascinating and clear explanation of how molecular motors walk and transport materials inside human cells.

dghughesin Hacker News • Recommends

On “Alzheimer’s treatment fully restores memory function (2015)”

…better. They made the hinge part of the foot work normally giving it more strength. It was a single phosphate molecule added to this step. It was incredible to think one small part of a protein motor the "ankle" part of the foot of that one protein motor on a microtubule inside a single cell had some help. I explained it horribly here is the video link to this video edit: phosphate not sulphur…

dopylittyin Hacker News • Recommends

On “Tardigrades Walk”

If you think that’s cool you might also like to see the motor proteins that walk along inside our cells. There are a few types including the ones that make muscles work. Kinesin is fun because it has little legs made of proteins. It gloms onto big bubbles of stuff inside the cell and carries them along pathways to their destination. Chemical reactions cause the proteins to fold in the right way to take each step. This shows how they look. link This explains the mechanisms that they use to walk. link to this video

shagiein Hacker News • Recommends

On “Rendering protein structures inside cells at the atomic level with Unreal Engine”

link I didn't realize there was also a Powering the Cell: Mitochondria video. The classic one narrated - link One of my pandemic YouTube binges was watching Ron Vale videos about kinesin and dynein. link to this video link link And searching for Ron Vale will bring a number of other videos about molecular machines.

trevynin Hacker News • Disputes

On “Consciousness Isn’t Self-Centered”

I only see simple biochemical machines in that video. Here’s what they look like when you zoom in a bit more: link to this video It’s literally chemical bonds breaking and forming, stochastically.

gilbetronin Hacker News • Mentions

On “The Wuhan Virus”

…other machines, that read that code in a different way, to create other machines, that copy that code, which is then read by other machines, etc, etc. These "machines" are chunks of molecules that require quantum mechanics to fully understand, and also tend to have a lot of issues with them. As an example of the weirdness, look at motor proteins: link to this video It's amazing how utterly mad it all is, and yet not only does it work, our simple models of how it works have actually been helpful even though they were wrong. I mean, it's not like there's actually a single value in your DNA that is looked up by some "eyeball creation" machine when it determines the color of your eyes. Rather, there's a w…