Literature DB >> 14758922

Protofilament and hexagon: a three-dimensional mechanical model for the junctional complex in the erythrocyte membrane skeleton.

Lanping Amy Sung1, Carlos Vera.   

Abstract

It is a long-standing mystery why erythrocyte actin filaments in the junctional complex (JC) are uniformly approximately 37 nm and the membrane skeleton consists of hexagons. We have previously proposed that a "molecular ruler" formed by E-tropomodulin and tropomyosin 5 or 5b functions to generate protofilaments of 12 G actin under mechanical stress. Here, we illustrate that intrinsic properties of actin filaments, e.g., turns, chemical bonds, and dimensions of the helix, also favor fragmentation into protofilaments under mechanical stress. We further construct a mechanical model in that a pair of G actin is wrapped around by a split alpha and beta spectrin, which may spin to two potential positions, and stabilize to one when the tail end is restricted. A reinforced protofilament may function as a mechanical axis to anchor three (top, middle, and bottom) pairs of Sp. Each Sp pair may wrap around the protofilament with a wide dihedral angle (approximately 166.2 degrees) and a minimal axial distance (2.75 nm). Such three Sp pairs may spiral down (right handed) the protofilament from the pointed end with a dihedral angle of approximately 55.4 degrees in between the Sp pairs. This first three-dimensional model of JC may explain the hexagonal geometry of the erythrocyte membrane skeleton.

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Year:  2003        PMID: 14758922     DOI: 10.1114/1.1635820

Source DB:  PubMed          Journal:  Ann Biomed Eng        ISSN: 0090-6964            Impact factor:   3.934


  14 in total

Review 1.  Tropomodulins: pointed-end capping proteins that regulate actin filament architecture in diverse cell types.

Authors:  Sawako Yamashiro; David S Gokhin; Sumiko Kimura; Roberta B Nowak; Velia M Fowler
Journal:  Cytoskeleton (Hoboken)       Date:  2012-05-04

2.  Erythrocyte tropomodulin isoforms with and without the N-terminal actin-binding domain.

Authors:  Weijuan Yao; Lanping Amy Sung
Journal:  J Biol Chem       Date:  2010-07-30       Impact factor: 5.157

3.  Rac GTPases regulate the morphology and deformability of the erythrocyte cytoskeleton.

Authors:  Theodosia A Kalfa; Suvarnamala Pushkaran; Narla Mohandas; John H Hartwig; Velia M Fowler; James F Johnson; Clinton H Joiner; David A Williams; Yi Zheng
Journal:  Blood       Date:  2006-08-01       Impact factor: 22.113

4.  Spectrin folding versus unfolding reactions and RBC membrane stiffness.

Authors:  Qiang Zhu; Robert J Asaro
Journal:  Biophys J       Date:  2007-12-07       Impact factor: 4.033

5.  A hybrid model for erythrocyte membrane: a single unit of protein network coupled with lipid bilayer.

Authors:  Qiang Zhu; Carlos Vera; Robert J Asaro; Paul Sche; L Amy Sung
Journal:  Biophys J       Date:  2007-04-20       Impact factor: 4.033

6.  Multiscale simulation of erythrocyte membranes.

Authors:  Zhangli Peng; Robert J Asaro; Qiang Zhu
Journal:  Phys Rev E Stat Nonlin Soft Matter Phys       Date:  2010-03-04

7.  Red cell membrane disorders: structure meets function.

Authors:  Mary Risinger; Theodosia A Kalfa
Journal:  Blood       Date:  2020-09-10       Impact factor: 22.113

8.  Intertwined αβ spectrin meeting helical actin protofilament in the erythrocyte membrane skeleton: wrap-around vs. point-attachment.

Authors:  Paul Sche; Carlos Vera; L Amy Sung
Journal:  Ann Biomed Eng       Date:  2011-03-17       Impact factor: 3.934

9.  Rac GTPases in erythroid biology.

Authors:  D G Konstantinidis; A George; T A Kalfa
Journal:  Transfus Clin Biol       Date:  2010-07-23       Impact factor: 1.406

10.  Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice.

Authors:  Raymond F Robledo; Steven L Ciciotte; Babette Gwynn; Kenneth E Sahr; Diana M Gilligan; Narla Mohandas; Luanne L Peters
Journal:  Blood       Date:  2008-08-22       Impact factor: 22.113

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