Proteins, recognition networks and developing interfaces for macromolecular biosensing

被引:5
作者
Sergi, M
Zurawski, J
Cocklin, S
Chaiken, I
机构
[1] Drexel Univ, Coll Med, Dept Biochem, Philadelphia, PA 19102 USA
[2] Drexel Univ, Coll Med, AJ Drexel Inst Basic & Appl Prot Sci, Philadelphia, PA 19102 USA
关键词
biosensors; coiled coil peptides; GPCRs; membranes; protein interactions; receptors; self-assembling interfaces;
D O I
10.1002/jmr.671
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genomics and proteomics discovery is leading to the identification of all proteins and to the opportunity, and challenge, to reveal the protein recognition networks that drive virtually all biological processes. Over the past decade, biosensors have emerged as a key technology for detection and analysis of biomolecular interactions. An important limitation in developing such biosensors is that the focus has been mainly on sensor platforms, the transducing hardware that converts interaction signals into recorded data, without adequately considering the role of molecular interfaces, the elements of sensors that interact with analytes to produce signals. We have investigated this alternative focus by identifying and, where necessary, designing molecular interfaces that will more effectively drive new biosensor development and utilization in biomedical and biotechnological investigations. Here we describe our recent studies of coiled coil and lipid bilayer interfaces and the potential to use these to expand sensing technologies for multiplexed target detection and analysis in increasingly biologically relevant membrane like environments. Copyright 2004 John Wiley Sons, Ltd.
引用
收藏
页码:198 / 208
页数:11
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