Encapsulation of proteins into human erythrocytes: a kinetic investigation

Abstract

Moderate osmotic shocks of human erythrocytes by hypotonic dialysis (0.06 mosmol/kg) induce cell swelling and formation of pores, without causing apparent lysis. Using 125I-labeled macromolecules of different molecular weight and net charge, we followed the kinetics and efficiency of their encapsulation into erythrocytes. After a 20–30 min period of cell dialysis, macromolecules of up to 50 kDa begin diffusing into the swollen cells by a process which can be described by a first-order two-compartment kinetics. Adsorption to the external cell surface was insignificant, while adsorption to the inner membrane surface was substantial (15–20%) only for positively charged proteins, at physiological pH. After resealing, pores of a 12–14 kDa cut-off might remain open allowing some release of entrapped material (20–30%), depending on the final cytocrit, while the remaining might be associated with inner membrane or cytosolic components. Although the method of hypotonic dialysis is known to affect minimally the biophysical and immunological properties of red blood cell membranes [1], the interaction of encapsulated material with cell constituents would need to be further assessed when considering red cells as macromolecular carriers.