2012
DOI: 10.1016/j.talanta.2012.08.020
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Fast human serum profiling through chemical depletion coupled to gold-nanoparticle-assisted protein separation

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Cited by 26 publications
(18 citation statements)
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“…Serum profiling using GNPs previously done in our laboratory has addressed a number of parameters that need to be optimized, as follow: (i) GNPs/protein ratio, (ii) pH range and (iii) incubation time. In addition, we have shown in previous work [23] that proteins with and without cysteine amino acids, a.a, can be separated one from each other using gold nanoparticles. Proteins without cysteine a.a. remain in the supernatant and can be further investigated, if necessary, as we have also recently shown [49].…”
Section: Optimization Of Urine Profiling Using Gold Nanoparticlesmentioning
confidence: 91%
See 1 more Smart Citation
“…Serum profiling using GNPs previously done in our laboratory has addressed a number of parameters that need to be optimized, as follow: (i) GNPs/protein ratio, (ii) pH range and (iii) incubation time. In addition, we have shown in previous work [23] that proteins with and without cysteine amino acids, a.a, can be separated one from each other using gold nanoparticles. Proteins without cysteine a.a. remain in the supernatant and can be further investigated, if necessary, as we have also recently shown [49].…”
Section: Optimization Of Urine Profiling Using Gold Nanoparticlesmentioning
confidence: 91%
“…In previous studies we have described a high-throughput method for serum proteomic profiling in patients with multiple myeloma [23]. In the present work such method has been optimized and applied to the complexity of urine samples.…”
Section: Introductionmentioning
confidence: 99%
“…An internal standard allows product quantification, using a-cyano-4-hydroxicinnamic acid (CHCA) as an organic matrix for MALDI-TOF. Following a similar principle, López-Cortes et al [13] have utilized AuNPs to separate serum proteins for subsequent fingerprinting identification by MALDI-TOF-MS. A mixture of 14 nm and 3.5 nm citrate-capped AuNPs was used for separation and analysis of biomolecules containing thiol groups, as the thiol groups show high affinity toward the gold surface and binding is strong and extremely likely to occur [14]. Aptamer-gold nanoparticle conjugates have also been used as affinity probes for SALDI-TOF analysis of adenosine triphosphate (ATP) and glutathione (GSH), improving sensitivity when compared to traditional matrices [15] -see Fig.…”
Section: Unmodified and Modified Nanoparticles For Sample Preparationmentioning
confidence: 99%
“…Other NPs, such as graphitized carbon NPs, have been used for SALDI-TOF/TOF-MS quantification of citrulline [73] via a novel method of tandem MS-parallel fragmentation monitoring (PFM) using graphitized carbon NPs as a surface for LDI. This way, it was possible to quantify citrulline and an isotopic analog that is 1 mass unit Handbook of Nanoparticles DOI 10.1007/978-3-319-13188-7_32-1 # Springer International Publishing Switzerland 2015 heavier ([ureido- 13 C] citrulline). Another approach used graphene-coated cobalt NPs functionalized with benzylamine groups for target enrichment and subsequent direct SALDI analysis of organic compounds [85].…”
Section: Carbon-containing Nanoparticlesmentioning
confidence: 99%
“…The functionality of MALDIViz application is demonstrated by analysis of in-house-generated screening data from an investigation of different solid-phase extraction (SPE) materials 17 and a publicly available cancer dataset. 18 The MALDIViz application is accessible through https://jkkishore85.shinyapps.io/maldiviz/.…”
Section: Introductionmentioning
confidence: 99%