The molecular mechanism of the ligand exchange reaction of an antibody against a glutathione-coated gold cluster
Nanoscale, ISSN: 2040-3372, Vol: 9, Issue: 9, Page: 3121-3127
2017
- 15Citations
- 27Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations15
- Citation Indexes15
- CrossRef15
- 15
- Captures27
- Readers27
- 27
Article Description
The labeling of proteins with heavy atom clusters is of paramount importance in biomedical research, but its detailed molecular mechanism remains unknown. Here we uncover it for the particular case of the anti-influenza N9 neuraminidase NC10 antibody against a glutathione-coated gold cluster by means of ab initio QM/MM calculations. We show that the labeling reaction follows an associative double S2-like reaction mechanism, involving a proton transfer, with low activation barriers only if one of the two distinct peptide/peptidic ligands (the one that occupies the side position) is substituted. Positively charged residues in the vicinity of the incoming thiol result in strong interactions between the antibody and the AuMPC, favoring the ligand exchange reaction for suitable protein mutants. These results pave the way for future investigations aimed at engineering biomolecules to increase their reactivity towards a desired gold atom cluster.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85014527126&origin=inward; http://dx.doi.org/10.1039/c6nr08498b; http://www.ncbi.nlm.nih.gov/pubmed/28210717; http://xlink.rsc.org/?DOI=C6NR08498B; http://pubs.rsc.org/en/content/articlepdf/2017/NR/C6NR08498B; https://xlink.rsc.org/?DOI=C6NR08498B; https://dx.doi.org/10.1039/c6nr08498b; https://pubs.rsc.org/en/content/articlelanding/2017/nr/c6nr08498b
Royal Society of Chemistry (RSC)
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