Tethering forces of secretory granules measured with optical tweezers.

Abstract:

:Fusion of a vesicle with its target membrane is preceded by tethering or docking. However, the physical mechanism of vesicle-tethering is unknown. To study this mechanism, we used eosinophil secretory granules, which undergo stimulated homotypic fusion events inside the cell during degranulation. Using a dual optical trap system, we observed tether formation between isolated eosinophil secretory granules. The results show that secretory granules interact stochastically with a target membrane forming physical tethers linking the vesicle and target membrane, rather than via interactions with the cytoskeleton. The necessary components are membrane-associated, and the addition of cytosolic components is not required. Tether-lifetime measurements as a function of applied mechanical force revealed at least three kinetically distinct tethered states. The tethered-state lifetimes of isolated eosinophil granules match the residence times of chromaffin granules at the plasma membrane in intact cells, suggesting that the tethering mechanisms reported here may represent the physiological mechanisms of vesicle-tethering in the cell.

journal_name

Biophys J

journal_title

Biophysical journal

authors

Valero V,Nevian T,Ho D,Lindau M

doi

10.1529/biophysj.108.132670

subject

Has Abstract

pub_date

2008-11-15 00:00:00

pages

4972-8

issue

10

eissn

0006-3495

issn

1542-0086

pii

S0006-3495(08)78635-1

journal_volume

95

pub_type

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