Key result
Immunomagnetic sorting yields highly purified platelet granules compared to traditional centrifugation and sedimentation.
Why the study?
Purification protocols for platelet dense and alpha granules are limited, necessitating improved methods for functional analysis of these intracellular structures.
This paper provides protocols for the isolation and purification of platelet dense and alpha granules, highlighting immunomagnetic sorting for high purity.
New protocols enable platelet alpha and dense granule isolation; leaves open their utility in cardiovascular research pending validation.
Functional analysis of platelet intracellular structures requires isolation and purification of these cellular compartments. With regard to the function of platelets, both, dense (delta) and alpha granules are relevant target structures. However, the availability of sufficient purification protocols for these structures is rather limited. This unit describes two protocols for isolation and purification of platelet granule structures. The Basic Protocol describes a new technique based on immunolabeling with target-specific antibodies followed by magnetic sorting, whereas the Alternate Protocol describes the more traditional procedure based on differential centrifugation and density-based sedimentation. For both methods, the degree of granule purification can be most easily determined by immunoblotting using various antibodies that recognize structure-specific proteins. The immunomagnetic sorting method is especially good for studies requiring highly purified material (e.g., for the identification of specific transporters and receptors).
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Nießen et al. (2010) studied this question. Immunomagnetic sorting vs. Differential centrifugation and density-based sedimentation was evaluated on Degree of granule purification. Immunomagnetic sorting using target-specific antibodies provides highly purified platelet granule material compared to traditional differential centrifugation and density-based sedimentation.
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