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Controllable g5p-Protein-Directed Aggregation of ssDNA-Gold Nanoparticles

Journal Article · · Langmuir
DOI:https://doi.org/10.1021/la803596q· OSTI ID:980082

We assembled single-stranded DNA (ssDNA) conjugated nanoparticles using the phage M13 gene 5 protein (g5p) as the molecular glue to bind two antiparallel noncomplementary ssDNA strands. The entire process was controlled tightly by the concentration of the g5p protein and the presence of double-stranded DNA. The g5p-ssDNA aggregate was disintegrated by hybridization with complementary ssDNA (C-ssDNA) that triggers the dissociation of the complex. Polyhistidine-tagged g5p was bound to nickel nitrilotriacetic acid (Ni2+-NTA) conjugated nanoparticles and subsequently used to coassemble the ssDNA-conjugated nanoparticles into multiparticle-type aggregates. Our approach offers great promise for designing biologically functional, controllable protein/nanoparticle composites.

Research Organization:
Brookhaven National Laboratory (BNL) National Synchrotron Light Source
Sponsoring Organization:
Doe - Office Of Science
DOE Contract Number:
AC02-98CH10886
OSTI ID:
980082
Report Number(s):
BNL--93000-2010-JA
Journal Information:
Langmuir, Journal Name: Langmuir Journal Issue: 2 Vol. 25; ISSN LANGD5; ISSN 0743-7463
Country of Publication:
United States
Language:
English

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