On a first glance, bacterial cell division may seem simple. In reality, it is the culmination of precisely orchestrated interplay between cytoplasmic and extracellular processes. #EngageDBIO#DBIOTweetorial
To divide, bacteria must: grow, replicate and segregate their chromosome, add new cell wall perpendicular to the old cell wall, and separate. That’s a lot of work! #EngageDBIO#DBIOTweetorial
One protein, FtsZ (in magenta below), is the star of bacterial cell division. FtsZ is a tubulin homologue that polymerizes in the presence of GTP to form a platform for the rest of the division machinery. Image courtesy of Jessie Bullock. #EngageDBIO#DBIOTweetorial
Once the cell grows to the proper size and chromosome replication is complete, FtsZ polymerizes into short polymers around the inner circumference of the cell. These polymers treadmill, just like tubulin! #EngageDBIO#DBIOTweetorial
FtsZ treadmilling ensures new cell wall is added evenly at the division site. This figure from Dr. @fleshball and colleagues shows old cell wall in blue and new cross wall labeled first in green and finally red. #EngageDBIO#DBIOTweetorialdoi.org/10.1126/scienc…
A cell has reached the right size for division when each relevant division protein is present in the correct *number* at the septum to proceed. Interestingly, this depends on the number of each protein present, not their cellular concentration. #EngageDBIO#DBIOTweetorial
Rather than being directed to the future division site by a mark of some kind, in many bacteria FtsZ is kept *away* from the cell poles and the chromosome by numerous factors that corral the division protein to midcell. #EngageDBIO#DBIOTweetorial
Some aspects of cell division remain unclear. For example, the mechanisms ensuring that the gram-negative outer membrane, which is external to the newly made cross wall, divides along with the rest of cell envelope are not entirely clear. #EngageDBIO#DBIOTweetorial
@taekjip is taking over @ApsDbio today to run a tweetorial titled 'single is good but a couple is better'.
Single molecule methods are allowing direct detection of subpopulations & dynamics, and correlation between multiple observables, with rapidly rising popularity. Technical milestones in single molecule fluorescence can be seen here.
Many flavors of single molecule methods. (1) fluorescence (2) mechanical (3) electrical & (4) in silico. All four have been honored by Nobel prizes in physics, chemistry and physiology.
It’s Tweetorial Thursday, so time for a #DBIOtweetorial, brought to you by the fantastic #engageDBIO team! Guest this week @SulianaManley, on why there is “No free lunch in microscopy”
For biophysicists, microscopy is a major tool and an exciting outlet for innovation. If you are a microscopy user more than a developer, it can seem like a major new method is published every week! Even just considering localization microscopy ...
So, how do we make sense of all this method development, and what is driving it? Sometimes developers chase world records in spatial resolution, temporal resolution, depth, or long-term imaging.
Like a city, inside of the cell is organised by highways and roads (microtubules, actin), motors (dynein, kinesins, myosins) cargoes (e.g. receptors in endosomes, viruses) post-offices sorting cargoes (sorting endosomes), garbage clean-up (autophagosomes, lysosomes) and much more
Every piece of the puzzle listed above is a field on its own! We now know about the exquisite dynamics of microtubules, or how motors move. We know about the process of endocytosis at the plasma membrane and proteins that define distinct endosomal populations (Rabs)