2006
DOI: 10.2174/157341306776875794
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Interfacing "Soft" and "Hard" Matter with Exquisite Chemical Control

Abstract: Abstract. The present paper reviews the recent development of new chemical and biological technologies for the site-specific immobilization of proteins onto inorganic materials and their potential applications to the fields of micro and nanotechnology.

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Cited by 12 publications
(8 citation statements)
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“…In this review we have tried to show a representative sample of several applications of EPL to study protein structure and function, however the number of applications is starting to grow exponentially. For example, EPL shows special promise in the area of nanotechnology [126], were this mild ligation approach could be used for the site-specific immobilization of proteins onto nanoparticles [127] and solid supports [61]. Another field where EPL would prove increasingly useful is the development of complex protein-based therapeutics.…”
Section: Discussionmentioning
confidence: 99%
“…In this review we have tried to show a representative sample of several applications of EPL to study protein structure and function, however the number of applications is starting to grow exponentially. For example, EPL shows special promise in the area of nanotechnology [126], were this mild ligation approach could be used for the site-specific immobilization of proteins onto nanoparticles [127] and solid supports [61]. Another field where EPL would prove increasingly useful is the development of complex protein-based therapeutics.…”
Section: Discussionmentioning
confidence: 99%
“…One of the most frequently used strategies to prepare this type of microarray involves the use of monoclonal antibodies as specific protein capture reagents. Antibodies have been classically well suited for this task, since there are a large number of commercially available specific antibodies, which can be easily immobilized onto solid supports (4,(27)(28)(29)(30). However, the potential problems associated with the use of antibodies for chip assembly, which might manifest themselves through moderate expression yields and by issues related to the stability and solubility of these large proteins, have led to the exploration of alternative protein scaffolds as a source for new, more effective and stable protein capture reagents (24,31,32).…”
Section: Protein-detecting Microarraysmentioning
confidence: 99%
“…Key to these methods is the introduction of a unique reacting group at a defined position in the protein to be immobilized, which can later react in a chemoselective manner with a complementary group previously introduced into the surface (Fig. 3 , see also references ( 4 , 27 , 29 , 69 , 78 ) for recent reviews).…”
Section: Novel Approaches For Protein Immobilizationmentioning
confidence: 99%
“…Moreover, the structural sensitivity of proteins calls for chemical transformations that proceed under mild conditions and are compatible with all functional groups present in proteins 1. 2, 12–15 The availability of a method for the fast, oriented, and covalent immobilization of expressed proteins from lysates would be of great value. This approach has been demonstrated previously on the basis of protein transsplicing,16, 17 phosphopantetheinyl transferase catalysis,18 and O 6 ‐alkylguanine‐DNA alkyltransferase (SNAP tag) 19.…”
mentioning
confidence: 99%