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Selection of Affibody Molecules Using Escherichia coli Display.

Authors :
Dahlsson Leitao C
Hjelm LC
Ståhl S
Löfblom J
Lindberg H
Source :
Cold Spring Harbor protocols [Cold Spring Harb Protoc] 2024 Nov 01; Vol. 2024 (11), pp. pdb.prot108400. Date of Electronic Publication: 2024 Nov 01.
Publication Year :
2024

Abstract

Affibody molecules are small (6-kDa) affinity proteins generated by directed evolution for specific binding to various target molecules. The first step in this workflow involves the generation of an affibody library, which can then be used for selection via multiple display methods. This protocol describes selection from affibody libraries by Escherichia coli cell surface display. With this method, high-diversity libraries of 10 <superscript>11</superscript> can be displayed on the cell surface. The method involves two steps for selection of binders from high-diversity libraries: magnetic-activated cell sorting (MACS) and fluorescence-activated cell sorting (FACS). MACS is used first to enrich the library in target-binding clones and to decrease diversity to a size that can be effectively screened and sorted in the flow cytometer in a reasonable time (typically <10 <superscript>7</superscript> cells). The protocol is based on methodology using an AIDA-I autotransporter for display on the outer membrane, but the general procedures can also be adjusted and used for other types of autotransporters or alternative E. coli display methods.<br /> (© 2024 Cold Spring Harbor Laboratory Press.)

Details

Language :
English
ISSN :
1559-6095
Volume :
2024
Issue :
11
Database :
MEDLINE
Journal :
Cold Spring Harbor protocols
Publication Type :
Academic Journal
Accession number :
37491079
Full Text :
https://doi.org/10.1101/pdb.prot108400