Related Experiment Videos
Lymphocyte surface receptors and albumin
Journal of Immunology (Baltimore, Md. : 1950)
|October 1, 1981
Summary
Researchers discovered albumin as a hidden component within mouse B and T lymphocyte plasma membranes. This finding, observed during immunoprecipitation, suggests potential implications for understanding lymphocyte biology.
Area of Science:
- Immunology
- Cell Biology
- Biochemistry
Background:
- Albumin is a common protein, but its presence within lymphocyte plasma membranes was previously unrecognized.
- Lymphocyte plasma membranes are critical for immune cell function and communication.
- Existing methods for studying membrane proteins may have overlooked cryptic components like albumin.
Purpose of the Study:
- To investigate the presence and accessibility of albumin within mouse B and T lymphocyte plasma membranes.
- To determine the methodologic implications of this cryptic albumin for immunological research.
- To explore the potential role of this albumin in lymphocyte biology.
Main Methods:
- Radiolabeling of lymphocyte plasma membranes using a lipophilic, photoactivated reagent (125I-iodonaphthylazide).
- Cell surface iodination using lactoperoxidase-catalyzed iodination.
- Immunofluorescence microscopy on intact cells.
- Immunoprecipitation experiments utilizing anti-immunoglobulin (Ig) reagents.
Main Results:
- Albumin was successfully radiolabeled from within the plasma membrane, indicating an internal localization.
- Albumin was not labeled from the cell exterior, confirming its cryptic nature.
- Albumin was not detected by immunofluorescence on intact cells, further supporting its hidden status.
- Contaminating albumin activity was identified in various antisera used in immunoprecipitation.
Conclusions:
- Albumin exists as a cryptic component of mouse B and T lymphocyte plasma membranes.
- The accessibility of this albumin suggests it is located internally within the membrane.
- The presence of contaminating albumin in antisera has significant methodologic implications for interpreting immunoprecipitation data, potentially explaining previously reported "Ig-like heavy chains".