Development of a Chemoenzymatic-like and Photoswitchable Method for the High-Throughput creation of Protein Microarrays. Application to the Analysis of the Protein/Protein Interactions Involved in the YOP Virulon from Yersinia pestis.

Camarero, J A

Lawrence Livermore National Laboratory

关键词: Pathogens;    59 Basic Biological Sciences;    Proteins;    Virulence;   

DOI  :  10.2172/902262
RP-ID  :  UCRL-TR-227591
RP-ID  :  W-7405-ENG-48
RP-ID  :  902262

美国|英语

来源: UNT Digital Library

【 摘 要 】

Protein arrays are ideal tools for the rapid analysis of whole proteomes as well as for the development of reliable and cheap biosensors. The objective of this proposal is to develop a new ligand assisted ligation method based in the naturally occurring protein trans-splicing process. This method has been used for the generation of spatially addressable arrays of multiple protein components by standard micro-lithographic techniques. Key to our approach is the use of the protein trans-splicing process. This naturally occurring process allows the development of a truly generic and highly efficient method for the covalent attachment of proteins through its C-terminus to any solid support. This technology has been used for the creation of protein chips containing several virulence factors from the human pathogen Y. pestis.