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Site-specific and reversible anchoring of active proteins onto cellulose using a cellulosome-like complex

Eklund, Malin (författare)
KTH,Bioteknologi
Sandström, Kristofer (författare)
KTH,Bioteknologi
Teeri, Tuula (författare)
KTH,Bioteknologi
visa fler...
Nygren, Per-Åke (författare)
KTH,Bioteknologi
visa färre...
 (creator_code:org_t)
Elsevier BV, 2004
2004
Engelska.
Ingår i: Journal of Biotechnology. - : Elsevier BV. - 0168-1656 .- 1873-4863. ; 109:3, s. 277-286
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Protein engineering strategies facilitating controlled and spontaneous assembly of macromolecular complexes are of great interest for the design of artificial multi-enzyme systems of pre-defined composition. Here we have combined affinity proteins from different sources to achieve specific and reversible anchoring of affinity domain-tagged reporter proteins to a cell ulose-anchored fusion protein. The design principle mimics the architecture of macromolecular cellulosome complexes produced by some cellulolytic microbes. A fusion protein between a cellulose-binding module (CBM1(Cel6A)) of the Trichoderma reesei cellobiohydrolase Cel6A and a five-domain staphylococcal protein A (SPA) was constructed to serve as platform for docking of easily detectable reporter proteins onto cellulose surfaces. In turn, the reporter proteins were produced as fusions to two copies of a SPA-binding affinity protein (an affibody denoted Z(SPA-1)), selected from a phage display library constructed by combinatorial protein engineering. In a series of experiments, involving repeated washing and low pH elution, affinity-tagged Enhanced Green Fluorescent Protein (EGFP) and Fusarium solani pisi lipase cutinase reporter proteins were both found to be specifically directed from solution to the same region of a cellulose filter paper where SPA-CBM1(Cel6A) fusion protein had been previously applied. This showed that the SPA-CBM1(Cel6A) fusion protein had been stably anchored to the cellulose surface without loss of binding capacity and that the interaction between SPA and the Z(SPA-1) affibody domains was selective. The generality of this biospecificity-driven system for assembly applications is discussed.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Nyckelord

cellulosome
assembly
affibody
affinity gene fusion
protein engineering
cellulose
bacterial receptor domain
binding domain
combinatorial library
degradation
expression
machines
affibody
chimeras
peptides
systems

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Eklund, Malin
Sandström, Krist ...
Teeri, Tuula
Nygren, Per-Åke
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NATURVETENSKAP
NATURVETENSKAP
och Biologi
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Kungliga Tekniska Högskolan

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