Result: A simple modification of the Q-plate for parallel screening and combinatorial crystallization

Title:
A simple modification of the Q-plate for parallel screening and combinatorial crystallization
Authors:
Source:
ICCBM-8: Proceedings of the Eighth International Conference on Crystallization of Biological Macromolecules, Sandestin, Florida, 14-19 May 2000Journal of crystal growth. 232(1-4):545-552
Publisher Information:
Amsterdam: Elsevier, 2001.
Publication Year:
2001
Physical Description:
print, 4 ref
Original Material:
INIST-CNRS
Document Type:
Conference Conference Paper
File Description:
text
Language:
English
Author Affiliations:
Département d'Ingénierie et d'Etudes des Protéines (DIEP), Commissariat à l'Energie Atomique (CEA), C.E. Saclay, 91191 Gif-sur-Yvette, France
ISSN:
0022-0248
Rights:
Copyright 2001 INIST-CNRS
CC BY 4.0
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
Notes:
Analytical, structural and metabolic biochemistry
Accession Number:
edscal.1133585
Database:
PASCAL Archive

Further Information

In many cases it can be advantageous to screen crystallization conditions in parallel. Tasks, such as the setting up a standard screen for several proteins simultaneously or analyzing the effect of drop size and different precipitant-protein drop ratios can be done more efficiently when drops are set up in parallel using a common reservoir. However, a real need for parallel screening becomes apparent when analyzing a large number of different complexes of the same protein, or when using methods such as stoichiometry variation screening and other combinatorial crystallization methods. Because of its large size, the Q-plate is easily adapted to the screening of a variable number of sitting drops in parallel. The drops are set up on a single glass slide placed over the same reservoir solution. The modification is simple and does not require a robot although it is well suited for automation. A record of each drop in multi-drop setup is kept as an HTML-file which allows for rapid navigation between experiments. Flexibility in the number drops makes the method effective for most combinatorial and non-combinatorial applications.