Preparation, Crystallization and Preliminary X-Ray Analysis of the Fab Fragment of Monoclonal Antibody MN423, Revealing the Structural Aspects of Alzheimers Paired Helical Filaments
Author(s) -
Natalia Csokova,
Rostislav Škrabana,
L. Urbanikova,
Branislav Kováčech,
А. Н. Попов,
Jozef Ševčı́k,
M. Novák
Publication year - 2006
Publication title -
protein and peptide letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 58
eISSN - 1875-5305
pISSN - 0929-8665
DOI - 10.2174/092986606778256180
Subject(s) - crystallization , crystallography , monoclonal antibody , chemistry , immunoglobulin fab fragments , molecule , alzheimer's disease , fragment (logic) , antibody , x ray , helix (gastropod) , biophysics , medicine , pathology , biology , disease , physics , immunology , organic chemistry , quantum mechanics , computer science , complementarity determining region , ecology , snail , programming language
Monoclonal antibody (mAb) MN423 recognizes Alzheimer's disease specific conformation of tau protein assembled into paired helical filaments (PHF). Since the three-dimensional structure of PHF is currently unavailable, the structure of MN423 binding site could provide important information about PHF conformation with the consequences for the Alzheimer's disease prevention and cure. Fab fragment of MN423 was prepared and purified. We have identified two different conditions for crystallization of the Fab fragment that yielded two crystal forms. They diffracted to 3.0 and 1.6 A resolution with four and one molecule in the asymmetric unit, respectively. Both crystal forms belonged to the space group P2(1) with unit cell parameters a = 76.4 A, b = 138.4 A, c = 92.4 A, beta = 101.9 degrees , and a = 71.5 A, b = 36.8 A, c = 85.5 A, beta = 113.9 degrees .
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