Research Topics
| K C ChanSummaryAffiliation: National Cancer Institute Country: USA Publications
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Detail Information
Publications
High-speed screening of polymerase chain reaction products by capillary electrophoresisK C Chan
Chemical Synthesis and Analysis Laboratory, SAIC Frederick, National Cancer Institute Frederick Cancer Research and Development Center, Maryland 21702, USA
Anal Biochem 243:133-9. 1996..This high-speed separation, with minimum postrun data processing, is highly desirable for the high-throughput screening of PCR products using a single-capillary CE system...
Analysis of fullerene-based nanomaterial in serum matrix by CEKing C Chan
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick Inc, NCI Frederick, Frederick, MD 21702, USA
Electrophoresis 28:1518-24. 2007..The quantitation of the nanoparticles was linear from 0-500 microg/mL with detection limits ranging from 0.5 to 6 microg/mL...
The effect of column length, applied voltage, gel type, and concentration on the capillary electrophoresis separation of DNA fragments and polymerase chain reaction productsH J Issaq
SAIC Frederik, NCI Frederick Cancer Research and Development Center, MD 21702, USA
Electrophoresis 18:1153-8. 1997..The Sigma DNA replaceable gel gave reproducible results when used as received or diluted at 60%. In our hands hydroxyethyl cellulose gave more reproducible results than polyacrylamide gel...
A simple two-dimensional high performance liquid chromatography/high performance capillary electrophoresis set-up for the separation of complex mixturesH J Issaq
SAIC Frederick, NCI Frederick Cancer Research and Development Center, MD 21702, USA
Electrophoresis 20:1533-7. 1999..This set-up is practical, simple, robust and allows the separation of complex mixtures. Preliminary results show the utility of this system for the analysis of protein digest...
Solid-state UV laser-induced fluorescence detection in capillary electrophoresisK C Chan
Analytical Chemistry Laboratory, SAIC Frederick, NCI Frederick Cancer Research and Development Center, MD 21702, USA
Electrophoresis 21:2062-6. 2000..Amino acids at a concentration as low as 10 ng/mL could be labeled with fluorescamine. Solid-state UV-LIF detection of the tryptic digest of cytochrome c after fluorescamine derivatization was demonstrated...
Effect of temperature on the separation of DNA fragments by high-performance liquid chromatography and capillary electrophoresis: a comparative studyH J Issaq
SAIC Frederick, NCI Frederick Cancer Research and Development Center, MD 21702, USA
J Chromatogr B Biomed Sci Appl 738:243-8. 2000..Also, the optimum HPLC temperature might be different depending on the fragment sizes to be resolved...
Separation of tryptophan and related indoles by micellar electrokinetic chromatography with KrF laser-induced fluorescence detectionK C Chan
SAIC Frederick, National Cancer Institute, Frederick Cancer Research and Development Center, MD 21702, USA
J Chromatogr A 718:203-10. 1995..Preliminary results show that the MEKC-LIF with direct sample injection is a feasible method for assessing indole profiles in diluted urine and serum...
Multidimensional high performance liquid chromatography--capillary electrophoresis separation of a protein digest: an updateH J Issaq
Analytical Chemistry Laboratory, SAIC Frederick, National Cancer Institute at Frederick, MD 21702, USA
Electrophoresis 22:1133-5. 2001..The total experimental time for the HPLC and capillary electrophoretic analyses ist less than 1 h, which ist much faster than using 2-D slab-gel electrophoresis or single-capillary capillary electrophoresis...
Quantitative profiling of the detergent-resistant membrane proteome of iota-b toxin induced vero cellsJosip Blonder
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc, National Cancer Institute at Frederick, P.O. Box B, Frederick, Maryland 21702-1201, USA
J Proteome Res 4:523-31. 2005..The quantitative profiling of Ib-induced DRMP from Vero cells revealed several proteins with altered expression levels suggesting their possible role in Ib binding/uptake...
Quantitative analysis of the low molecular weight serum proteome using 18O stable isotope labeling in a lung tumor xenograft mouse modelBrian L Hood
Laboratory of Proteomics and Analytical Technologies, National Cancer Institute at Frederick, SAIC-Frederick, Inc, Frederick, Maryland 21702, USA
J Am Soc Mass Spectrom 16:1221-30. 2005..The methodology adopted in this work provides the means for future quantitative measurements in comparative animal models of disease and in human disease cohorts...
Investigation of the mouse serum proteomeBrian L Hood
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc, National Cancer Institute at Frederick, PO Box B, Frederick, MD 21702, USA
J Proteome Res 4:1561-8. 2005..The results presented here represent the broadest proteome coverage in mouse serum and provide a foundation from which quantitative comparisons can be made in this important animal model...
Combined chemical and enzymatic stable isotope labeling for quantitative profiling of detergent-insoluble membrane proteins isolated using Triton X-100 and Brij-96Josip Blonder
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick, Inc, National Cancer Institute at Frederick, Frederick, Maryland 21702 1201, USA
J Proteome Res 5:349-60. 2006..This result confirms previous, targeted studies suggesting that DRMMs isolated using Triton X-100 and Brij-96 differ in their protein content...
Identification of the SELDI ProteinChip human serum retentate by microcapillary liquid chromatography-tandem mass spectrometryMing Zhou
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc, National Cancer Institute at Frederick, P.O. Box B, Frederick, Maryland 21702, USA
J Proteome Res 5:2207-16. 2006..This analysis resulted in the identification of 383 unique proteins in the WCX-2 serum retentate. Among the proteins identified, 50 (13%) are documented clinical biomarkers with 36 of these (72%) identified from multiple peptides...
Mass spectrometry reveals specific and global molecular transformations during viral infectionEden P Go
Department of Molecular Biology and The Center for Mass Spectrometry, The Scripps Research Institute, La Jolla, California 92037, USA
J Proteome Res 5:2405-16. 2006..Overall, the cellular transformation that occurs upon viral infection is a process involving hundreds of proteins and metabolites, many of which are structurally and functionally uncharacterized...
Proteomic analysis of plasma membrane from hypoxia-adapted malignant melanomaLuke H Stockwin
Drug Mechanisms Group and Laboratory of Proteomics and Analytical Technologies, SAIC Frederick Inc, National Cancer Institute at Frederick, Frederick, Maryland 21702, USA
J Proteome Res 5:2996-3007. 2006..Antibody-based analysis of a panel of human melanoma cell lines confirmed that CD13 and SDF-1 were consistently upregulated during hypoxia. This study provides the basis for the discovery of novel hypoxia-induced membrane proteins...
Quantitative proteomic analysis of human breast epithelial cells with differential telomere lengthLi Rong Yu
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick, Inc, NCI Frederick, Frederick, Maryland 21702, USA
Biochem Biophys Res Commun 356:942-7. 2007..Interestingly, the DNA excision repair pathway is enhanced, while integrin and its ligands are downregulated in the cells with long telomeres. These results may provide valuable information related to telomere functions...
Identification of membrane proteins from mammalian cell/tissue using methanol-facilitated solubilization and tryptic digestion coupled with 2D-LC-MS/MSJosip Blonder
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick, Inc, National Cancer Institute at Frederick, P O Box B, Frederick, Maryland 21702, USA
Nat Protoc 1:2784-90. 2006..The entire procedure--beginning with isolated membrane fraction and finishing with MS data acquisition--takes 4-5 d...
Multidimensional separation of peptides for effective proteomic analysisHaleem J Issaq
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick Inc, National Cancer Institute at Frederick, P O Box B, Frederick, Maryland, MA 21702, USA
J Chromatogr B Analyt Technol Biomed Life Sci 817:35-47. 2005..This manuscript provides a review of two- and three-dimensional peptide separation strategies combined with MS for the analysis of complex peptide mixtures...
Quantitative proteomic analysis of sokotrasterol sulfate-stimulated primary human endothelial cellsAly Karsan
Department of Medical Biophysics, British Columbia Cancer Agency, Vancouver, British Columbia V5Z 1L3, Canada
Mol Cell Proteomics 4:191-204. 2005..These findings are consistent with a role for sokotrasterol sulfate in endothelial sprouting...
An investigation into the human serum "interactome"Ming Zhou
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick, Inc, National Cancer Institute, Frederick, MD, USA
Electrophoresis 25:1289-98. 2004..Among the 210 proteins identified, 73% and 67% were not found in previous studies of the low-molecular-weight or whole-serum proteome, respectively...
Global analysis of the cortical neuron proteomeLi-Rong Yu
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc, National Cancer Institute at Frederick, P.O. Box B, Frederick, MD 21702-1201, USA
Mol Cell Proteomics 3:896-907. 2004..The results presented here provide the broadest proteome coverage for a mammalian cell to date and show that MS-based proteomics has the potential to provide high coverage of the proteins expressed within a cell...
Two-dimensional liquid chromatography-capillary zone electrophoresis-sheathless electrospray ionization-mass spectrometry: evaluation for peptide analysis and protein identificationGeorge M Janini
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick Inc, National Cancer Institute, National Institutes of Health, Frederick, MD 21702 1201, USA
Electrophoresis 25:1973-80. 2004..Unlike first-dimensional ion-exchange LC fractionation, where there is a large degree of overlap, the CZE-MS results show less than 15% overlap between neighboring RPLC fractions...
Improved titanium dioxide enrichment of phosphopeptides from HeLa cells and high confident phosphopeptide identification by cross-validation of MS/MS and MS/MS/MS spectraLi Rong Yu
Laboratory of Proteomics and Analytical Technologies, Advanced Technology Program, SAIC Frederick, Inc, NCI Frederick, P O Box B, Frederick, Maryland 21702, USA
J Proteome Res 6:4150-62. 2007..The study also indicates that evaluation of confidence levels for phosphopeptide identification via the reversed sequence database searching strategy might underestimate the false positive rate...
Analysis of murine natural killer cell microsomal proteins using two-dimensional liquid chromatography coupled to tandem electrospray ionization mass spectrometryJosip Blonder
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc, Frederick, Maryland 21702-1201, USA
J Proteome Res 3:862-70. 2004..These peptides resulted in identification of 2563 proteins of which 876 (34%) are classified as membrane proteins...
A proteomic characterization of the plasma membrane of human epidermis by high-throughput mass spectrometryJosip Blonder
Laboratory of Proteomics and Analytical Technologies, Mass Spectrometry Center, SAIC-Frederick, Inc, National Cancer Institute at Frederick, Frederick, Maryland, USA
J Invest Dermatol 123:691-9. 2004..Furthermore, 121 proteins from cholesterol-rich plasma membrane domains (caveolar and lipid rafts) were identified...
Sheathless electrospray ionization interfaces for capillary electrophoresis-mass spectrometric detection advantages and limitationsHaleem J Issaq
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick Inc, National Cancer Institute at Frederick, P O Box B, Frederick, MD 20702, USA
J Chromatogr A 1053:37-42. 2004..The advantages and limitations of three sheathless designs are discussed and commented upon, these include single-capillary, two-capillary and three-piece designs...
Two dimensional mapping of cancer cell extracts by liquid chromatography-capillary electrophoresis with ultraviolet absorbance detectionYan He
Ames Laboratory-USDOE and Department of Chemistry, Iowa State University, Ames, IA 50011, USA
J Chromatogr A 979:81-9. 2002..In this way, high-resolution analysis of even the minor components in the complicated mixture was possible...
Characterization of the low molecular weight human serum proteomeRadhakrishna S Tirumalai
SAIC-Frederick Inc, Laboratory of Proteomics and Analytical Technologies, Mass Spectrometry Center, National Cancer Institute at Frederick, Frederick, MD 21702-1201, USA
Mol Cell Proteomics 2:1096-103. 2003..The large number of proteins identified demonstrates the efficacy of this method for the removal of large abundant proteins and the enrichment of the LMW serum proteome...
Analysis of the extracellular matrix vesicle proteome in mineralizing osteoblastsZhen Xiao
Laboratory of Proteomics and Analytical Technologies, SAIC Frederick, Inc, NCI Frederick, Frederick, Maryland 21702, USA
J Cell Physiol 210:325-35. 2007..This investigation represents the first systematic proteomic analysis of MVs and provides insights into both the function and origin of these important mineralization-regulating vesicles...
Quantitative proteomic analysis of inorganic phosphate-induced murine MC3T3-E1 osteoblast cellsKelly A Conrads
Laboratory of Cancer Prevention, Center for Cancer Research, Fredrick, MD, USA
Electrophoresis 25:1342-52. 2004..41-fold increase as determined by Western blotting. These results demonstrate that quantitative proteomics is capable of providing a quantitative view of thousands of proteins in mammalian cells within a defined set of experiments...
Parallel analysis of transcript and translation profiles: identification of metastasis-related signal pathways differentially regulated by drug and genetic modificationsHaiyan Yang
Laboratory of Population Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892, USA
J Proteome Res 5:1555-67. 2006....
A capillary electrophoretic assay for ribonuclease H activityKing C Chan
Laboratory of Proteomics and Analytical Technologies, SAIC-Frederick, Inc, Center for Cancer Research, NCI at Frederick, Frederick, MD 21702, USA
Anal Biochem 331:296-302. 2004..The assay was broadly applicable to other RNases H, specifically those from human, Escherichia coli, and HIV-2, although product profiles varied for each enzyme...
