Reactivity Profiling: Covalent Modification of Single Nucleophile Peptides for Skin Sensitization Risk Assessment

被引:100
作者
Aleksic, Maja [1 ]
Thain, Emma [1 ]
Roger, Delphine [1 ]
Saib, Ouarda [1 ]
Davies, Michael [1 ]
Li, Jin [1 ]
Aptula, Aynur [1 ]
Zazzeroni, Raniero [1 ]
机构
[1] Unilever Colworth, Safety & Environm Assurance Ctr, Sharnbrook MK44 1LQ, Beds, England
关键词
skin sensitization; covalent binding; model peptide; mass spectrometry; in chemico; hapten; FORMALDEHYDE-INDUCED MODIFICATIONS; IN-VITRO PREDICTION; HUMAN SERUM-ALBUMIN; IDENTIFICATION; PROTEIN; ADDUCTS; POTENCY; BINDING; GLUTATHIONE; ALLERGENS;
D O I
10.1093/toxsci/kfp030
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The molecular basis of chemical allergy is rooted in the ability of an allergen (hapten) to modify endogenous proteins. This mechanistic understanding aided development of screening assays which generate reproducible quantitative and qualitative reactivity data. Such assays use model peptides with a limited number and type of protein nucleophiles, and the data does not reflect the specificity, variety, and complexity of hapten interactions with multiple nucleophiles. Building on these developments, we extended the standardized approach to maximize the type and the amount of information that can be derived from an in chemico assay. We used a panel of six single nucleophile peptides and individually optimized the incubation conditions to favor chemical modification. Employing liquid chromatography tandem mass spectrometry (LC-MS/MS) technique, we simultaneously obtained multiple quantitative and qualitative measurements (% peptide depletion, adducts formation, and peptide dimerization for Cys-containing peptide). Using these methods, we obtained reactivity data for 36 chemicals of known skin sensitizing potency. By optimizing incubation conditions, we ensured detection of all reactive chemicals. We explored the LC-MS/MS approach to generate kinetic data for 10 chemicals allowing further characterization of reactivity and a potentially more robust quantitative reactivity descriptor. Our ultimate aim is to integrate this dataset with available physicochemical data and outputs from other predictive assays, all addressing different key steps in the induction of sensitization, to help us make decisions about the safe use of chemicals without using animal tests. The epidermal protein target sites, modification of which may be immunogenic and lead to induction of skin sensitization, are currently unknown. Increasing the understanding of this process may help further refine in chemico reactivity assays as well as aid the interpretation of the reactivity data.
引用
收藏
页码:401 / 411
页数:11
相关论文
共 32 条
[1]   Mass spectrometric identification of covalent adducts of the skin allergen 2,4-dinitro-1-chlorobenzene and model skin proteins [J].
Aleksic, Maja ;
Pease, Camilla K. ;
Basketter, David A. ;
Panico, Maria ;
Morris, Howard R. ;
Dell, Anne .
TOXICOLOGY IN VITRO, 2008, 22 (05) :1169-1176
[2]   Investigating protein haptenation mechanisms of skin sensitisers using human serum albumin as a model protein [J].
Aleksic, Maja ;
Pease, Camilla K. ;
Basketter, David A. ;
Panico, Maria ;
Morris, Howard R. ;
Dell, Anne .
TOXICOLOGY IN VITRO, 2007, 21 (04) :723-733
[3]   Effect of glutathione on the covalent binding of the 13C-labeled skin sensitizer 5-chloro-2-methylisothiazol-3-one to human serum albumin:: Identification of adducts by nuclear magnetlic resonance, matrix-assisted laser desorption/ionization mass spectrometry, and nanoelectrospray tandem mass spectrometry [J].
Alvarez-Sánchez, R ;
Divkovic, M ;
Basketter, D ;
Pease, C ;
Panico, M ;
Dell, A ;
Morris, H ;
Lepoittevin, JP .
CHEMICAL RESEARCH IN TOXICOLOGY, 2004, 17 (09) :1280-1288
[4]   Final report on the safety assessment of benzaldehyde [J].
不详 .
INTERNATIONAL JOURNAL OF TOXICOLOGY, 2006, 25 :11-27
[5]   Non-enzymatic glutathione reactivity and in vitro toxicity: A non-animal approach to skin sensitization [J].
Aptula, AO ;
Patlewicz, G ;
Roberts, DW ;
Schultz, TW .
TOXICOLOGY IN VITRO, 2006, 20 (02) :239-247
[6]   Measurement of allergenic potency using the local lymph node assay [J].
Basketter, DA ;
Gerberick, GF ;
Kimber, I .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2001, 22 (06) :264-265
[7]   A skin-like cytochrome P450 cocktail activates prohaptens to contact allergenic metabolites [J].
Bergstrom, Moa Andresen ;
Ott, Hagen ;
Carlsson, Anna ;
Neis, Mark ;
Zwadlo-Klarwasser, Gabriele ;
Jonsson, Charlotte A. M. ;
Merk, Hans F. ;
Karlberg, Ann-Therese ;
Baron, Jens M. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2007, 127 (05) :1145-1153
[8]   Cytosolic and nuclear protein targets of thiol-reactive electrophiles [J].
Dennehy, MK ;
Richards, KAM ;
Wernke, GR ;
Shyr, Y ;
Liebler, DC .
CHEMICAL RESEARCH IN TOXICOLOGY, 2006, 19 (01) :20-29
[9]   Hapten-protein binding:: from theory to practical application in the in vitro prediction of skin sensitization [J].
Divkovic, M ;
Pease, CK ;
Gerberick, GF ;
Basketter, DA .
CONTACT DERMATITIS, 2005, 53 (04) :189-200
[10]   Drug-protein adducts: An industry perspective on minimizing the potential for drug bioactivation in drug discovery and development [J].
Evans, DC ;
Watt, AP ;
Nicoll-Griffith, DA ;
Baillie, TA .
CHEMICAL RESEARCH IN TOXICOLOGY, 2004, 17 (01) :3-16