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#plus end

2 public questions tagged with this topic.

In microtubule polymerization, which end exhibits faster growth?

Polarity of microtubules dictates directionality of transport and regulation by plus end tracking proteins +TIP network. Lattice assembled from head to tail alpha beta dimers creates structurally distinct ends with different chemistry. Minus end shows alpha tubulin outward typically embedded in gamma TuRC within MTOC exchange slow often capped by patronins CAMSAP family. Plus end exposes beta tubulin with GTP binding pocket capable of rapid subunit addition with on rate about 7 per micromolar per second versus minus about half. In vitro growth rates show plus about two to three fold faster elongation also more dynamic undergoing frequent catastrophe and rescue events regulated by EB1 XMAP215. In cells EB family and XMAP215 selectively accumulate at plus ends accelerating growth while minus dynamics dampened and stabilized. This asymmetry enables plus ends to explore cell periphery searching kinetochores and cortical capture sites while minus ends provide stable anchor for force generation during spindle formation and maintain organized radial arrays supporting polarized transport highways.

Ref: Alberts et al., Molecular Biology of the Cell, Chapter 14 – Plus end exhibits faster growth due to polarity.

The rate of ATP-actin addition is __ times faster at the (+) end compared to the (-) end.

Elongation kinetics at filament ends measured using TIRF microscopy of single filaments and pyrene actin assembly shows strong asymmetry. Barbed plus end characterized by high on rate constant 11.6 per micromolar per second and off rate 1.4 per second, critical concentration 0.12 micromolar, while pointed minus end on rate 1.3 per micromolar per second off rate 0.8 per second Cc 0.6 micromolar. Ratio on rates roughly nine fold, often approximated as ten fold faster at plus end for ATP actin at physiological ionic strength 50 millimolar KCl 1 millimolar MgCl2. ATP actin cap at plus end stabilizes, with ATP hydrolysis occurring after incorporation generating ADP Pi intermediate that still retains higher affinity than ADP. ADP actin at minus end less stable. Profilin ATP actin addition exclusive to plus end exaggerates bias in vivo. This kinetic difference drives treadmilling when free monomer between two Cc values, enables lamellipodial protrusion where plus ends face membrane, and underlies polarity dependent myosin directionality vital for cell migration and contractility.

Ref: Pollard and Earnshaw, Cell Biology, Chapter 12: Barbed End Kinetics and Actin Polarity.