Probing the effects of cysteine residues on protein adsorption onto gold nanoparticles using wild-type and mutated GB3 proteins

The role of cysteine residues in the protein binding kinetics and stability on gold nanoparticles (AuNP) was studied using AuNP localized surface plasmon resonance (LSPR) in combination with an organothiol (OT) displacement method. GB3, the third IgG-binding domain of protein G, was used to model pr...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 29(2013), 35 vom: 03. Sept., Seite 10990-6
1. Verfasser: Siriwardana, Kumudu (VerfasserIn)
Weitere Verfasser: Wang, Ailin, Vangala, Karthikeshwar, Fitzkee, Nicholas, Zhang, Dongmao
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, U.S. Gov't, Non-P.H.S. Bacterial Proteins IgG Fc-binding protein, Streptococcus Recombinant Proteins Sulfhydryl Reagents Gold 7440-57-5 Cysteine K848JZ4886
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100 1 |a Siriwardana, Kumudu  |e verfasserin  |4 aut 
245 1 0 |a Probing the effects of cysteine residues on protein adsorption onto gold nanoparticles using wild-type and mutated GB3 proteins 
264 1 |c 2013 
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520 |a The role of cysteine residues in the protein binding kinetics and stability on gold nanoparticles (AuNP) was studied using AuNP localized surface plasmon resonance (LSPR) in combination with an organothiol (OT) displacement method. GB3, the third IgG-binding domain of protein G, was used to model protein-AuNP adsorption. While wild-type GB3 (GB30) contains no cysteine residues, bioengineered GB3 variants containing one (GB31) and two (GB32) cysteine residues were also tested. The cysteine content has no significant effect on GB3 binding kinetics with AuNPs, and most protein adsorption occurs within the first few seconds upon protein/AuNP mixing. However, the stability of GB3 on the AuNP surface against OT displacement depends strongly on the cysteine content and the age of the AuNP/GB3 mixture. The GB30 covered AuNPs can be completely destabilized and aggregated by OTs, regardless of the age of the GB30/AuNP mixtures. Long-time incubation of GB31 or GB32 with AuNPs can stabilize AuNPs against the OT adsorption inducted aggregation. This study indicates that multiple forces involved in the GB3/AuNP interaction, and covalent binding between cysteine and AuNP is essential for a stable protein/AuNP complex 
650 4 |a Journal Article 
650 4 |a Research Support, U.S. Gov't, Non-P.H.S. 
650 7 |a Bacterial Proteins  |2 NLM 
650 7 |a IgG Fc-binding protein, Streptococcus  |2 NLM 
650 7 |a Recombinant Proteins  |2 NLM 
650 7 |a Sulfhydryl Reagents  |2 NLM 
650 7 |a Gold  |2 NLM 
650 7 |a 7440-57-5  |2 NLM 
650 7 |a Cysteine  |2 NLM 
650 7 |a K848JZ4886  |2 NLM 
700 1 |a Wang, Ailin  |e verfasserin  |4 aut 
700 1 |a Vangala, Karthikeshwar  |e verfasserin  |4 aut 
700 1 |a Fitzkee, Nicholas  |e verfasserin  |4 aut 
700 1 |a Zhang, Dongmao  |e verfasserin  |4 aut 
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773 1 8 |g volume:29  |g year:2013  |g number:35  |g day:03  |g month:09  |g pages:10990-6 
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