Optical tweezer for probing erythrocyte membrane deformability

We report that the average rotation speed of optically trapped crenated erythrocytes is direct signature of their membrane deformability. When placed in hypertonic buffer, discocytic erythrocytes are subjected to crenation. The deformation of cells brings in chirality and asymmetry in shape that makes them rotate under the scattering force of a linearly polarized optical trap. A change in the deformability of the erythrocytes, due to any internal or environmental factor, affects the rotation speed of the trapped crenated cells. Here we show how the increment in erythrocyte membrane rigidity with adsorption of Ca++ ions can be exhibited through this approach.

[1]  Chuan Li,et al.  Nanomechanical characterization of red blood cells using optical tweezers , 2008, Journal of materials science. Materials in medicine.

[2]  C. Rao,et al.  Optically driven nanorotors: experiments and model calculations. , 2007, Journal of nanoscience and nanotechnology.

[3]  C. Rao,et al.  Nanorotors using asymmetric inorganic nanorods in an optical trap , 2006 .

[4]  Subra Suresh,et al.  Viscoelasticity of the human red blood cell , 2006, American journal of physiology. Cell physiology.

[5]  S. Mohanty,et al.  Optically-driven red blood cell rotor in linearly polarized laser tweezers , 2005 .

[6]  Khyati Mohanty,et al.  Dynamics of Interaction of RBC with optical tweezers. , 2005, Optics express.

[7]  Shobhona Sharma,et al.  Naturally occurring, optically driven, cellular rotor , 2004 .

[8]  J. D. Bell,et al.  Divalent cations increase lipid order in erythrocytes and susceptibility to secretory phospholipase A2. , 2004, Biophysical journal.

[9]  C. Lim,et al.  Mechanics of the human red blood cell deformed by optical tweezers , 2003 .

[10]  A. Drochon Rheology of dilute suspensions of red blood cells: experimental and theoretical approaches , 2003 .

[11]  Ogobara K. Doumbo,et al.  The pathogenic basis of malaria , 2002, Nature.

[12]  A. Cowman,et al.  Contribution of parasite proteins to altered mechanical properties of malaria-infected red blood cells. , 2002, Blood.

[13]  Pál Ormos,et al.  Complex micromachines produced and driven by light , 2001, CLEO 2002.

[14]  B. Riquelme,et al.  Complex viscoelasticity of normal and lectin treated erythrocytes using laser diffractometry. , 1998, Biorheology.

[15]  E. Evans,et al.  Molecular maps of red cell deformation: hidden elasticity and in situ connectivity. , 1994, Science.

[16]  Christoph F. Schmidt,et al.  Conformation and elasticity of the isolated red blood cell membrane skeleton. , 1992, Biophysical journal.

[17]  E. Sackmann,et al.  On the measurement of shear elastic moduli and viscosities of erythrocyte plasma membranes by transient deformation in high frequency electric fields. , 1988, Biophysical journal.

[18]  E. Quist Regulation of erythrocyte membrane shape by Ca2+. , 1980, Biochemical and biophysical research communications.

[19]  S Chien,et al.  Theoretical and experimental studies on viscoelastic properties of erythrocyte membrane. , 1978, Biophysical journal.

[20]  K. Carraway,et al.  Calcium-promoted changes of the human erythrocyte membrane. Involvement of spectrin, transglutaminase, and a membrane-bound protease. , 1977, The Journal of biological chemistry.

[21]  R. Hochmuth,et al.  Viscosity of human red cell membrane in plastic flow. , 1976, Microvascular research.

[22]  J. Murphy,et al.  Physical properties of red cells as related to effects in vivo. I. Increased rigidity of erythrocytes as measured by viscosity of cells altered by chemical fixation, sickling and hypertonicity. , 1968, Blood.

[23]  A. Seiyama,et al.  Increased viscosity of erythrocyte suspension upon hemolysis , 1993 .

[24]  N. Maeda,et al.  Decreased viscosity of human erythrocyte suspension due to drug-induced spherostomatocytosis. , 1982, Biorheology.