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Carbohydrate microarrays for the recognition of cross-reactive molecular markers of microbes and host cells Denong Wang et al Presented by Chao Ji.

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Presentation on theme: "Carbohydrate microarrays for the recognition of cross-reactive molecular markers of microbes and host cells Denong Wang et al Presented by Chao Ji."— Presentation transcript:

1 Carbohydrate microarrays for the recognition of cross-reactive molecular markers of microbes and host cells Denong Wang et al Presented by Chao Ji

2 Carbohydrates play important role in microbe-host interaction (e.g. many epitopes are carbohydrates) A carbohydrate-based microarray system sensitive enough to be able to detect a wide range of antibodies specificities Is it feasible and good enough? – Whether carbohydrates can be immobilized on a glass surface without covalent bond – Whether immobilized carbohydrates preserve their immunological properties – Whether the proposed system reaches the sensitivity and capacity to detect a broad range of antibody specificities using only small quantities of sample – Whether it can be used to study carbohydrate interactions with high throughput

3 Structure of Dextran – Polymerization of glucose – Linear: α(1,6) – Branched: α(1,6), α(1,3) or α(1,2) –Representative of a variety of types of sugars – Recognizable by antibodies with different epitope specificity – Model system to immobilize carbohydrate antigens and study their immunological property

4 Nitrocellulose-coated glass slides can be used to immobilize carbohydrates without covalent bonds – FITC-conjugated dextrans of different MW and insulin were printed on slides – Dextran with MW 20kDa-2,000kDa stably immobilized non- covalently – Larger dextran molecules were better retained

5 Immunological properties of dextrans are well- preserved when immobilized on nitrocellulose coated slides – Carbohydrate antigens: N279, both internal linear and terminal non-reducing end; B1299S, heavily branched; LD7, 100% internal linear – Antibodies: IgG3(4.3F1), groove-type, targets internal linear α(1,6) chain; IgA(16.4.12E), cavity-type targets terminal non-reducing end strucuture

6 The carbohydrate arrays is sensitive enough for the detection of a broad spectrum of antibody specificities – 48 structurally distinct carbohydrate-containing macromolecules – 20 serum specimens, 1μl from each for staining – 12/48 specificities of IgM and 35/48 of IgG – A speculation based on IgG > IgM: naturally occurring anti-carbohydrate antibodies may be of IgG type

7 4 Classes 1 polysaccharide: 29 2 glycosaminoglycan: 3 3 glycoprotein: 11 4 semisynthetic glycoconjugate: 5

8 Characterizing previously unnkown specificity and cross-reactivity of carbohydrate/antibody interaction – 2 anti-dextran mAbs: 4.3.F1 and 16.4.12E applied on the same panel of carbohydrate – CS-B is recognized by 4.3.F1 (unexpectedly) because of its non- dominant structure rather than its dominant repeating disaccharide sequence of GalNAc(4S) – In vivo study showed the structure recognized by 4.3F1 is an endogenous cellular element – 4.3F1 staining is resistant to the pretreatment of tissue by dextranase – 45.21.1: another anti α(1-6) groove-type antibody that also reacted with CS-B 4.3.F116.4.12E BSA(E1),KLM(E2)NY CS-B(A6)YN

9 Conclusion A sensitive and efficient carbohydrate microarray with large capacity Only small quantity of specimen is necessary in the detection of antibody specificities Broad applicability in a wide range of biomedical research involving carbohydrate- based molecular recognition


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