Optimized adhesin fragments and corresponding nanoparticles
The invention relates to optimized adhesins and nanoparticles to which said adhesins are bound. The invention furthermore relates to providing said nanoparticles by way of in vivo contrast agents, in particular for the diagnosis of bowel cancer.
1. A method of preparing a contrast agent for medical use comprising the steps of:
providing an adhesin comprising an amino acid sequence selected from the group consisting of the following sequences,
DraE SEQ ID NO: 1
wherein said adhesin has one or more of the following mutations and is deleted N-terminally by up to 18 amino acids and/or C-terminally by up to 10 amino acids:
T7 (N, F, C, S, V, R, A, I, L, Y); E17 (S, P, K, G, D, R, N, H, Q); R22 (T, A, S, N, K); D25 (S, G, N, A, T, K, R, H, Q, M); T27 (K, R, L, V, Y, P, N, O); V28 (W, F); A29 (K, R, S, E, Q, F, G, L, H, P, N, T, W); T31 (G, D, S, N); Q34 (D, G, S, N, L, V, T, A); D37N; A38 (S, T, L); A39 (Q, S, D, M, G, F); I41 (V); Q47 (T, N, C, S, G, A, P); D52 (G, N, S, C, P, Q, Y, H, K, R, T); N84 (D, S, H); R86V; T88 (M, L); T95 (L, M, Y, F, C, W, Q, N, E, S, I, H); F100 (Y, V); V105 (S, A, T, R, M, V, P, N, E, Q, G, K, H); I111 (C, V, H, Y, T, M, F) I114 (V, L, A, C); Y115 (T, W, E, V); V116 (A, S, L); G118 (P, S),
combining the adhesin with a suitable carrier for use as a contrast agent in medical treatment.
2. The method of claim 1 , wherein the adhesin is conjugated to a nanoparticle.
3. The method of claim 2 , wherein the nanoparticle has an inorganic core and a passivation layer, with the smallest diameter of an inorganic core including the passivation layer being no more than 15 nm.
4. The method of claim 1 , wherein the adhesin is binding to the N-terminal sequence of a binding protein having an amino acid sequence selected from the group of the following sequences,
CEACAM group SEQ ID NO. 5
CEA/NCA SEQ ID NO. 6
CEA SEQ ID NO. 7 and/or NCA SEQ ID NO. 8.
5. The method of claim 1 , wherein said adhesin is deleted N-terminally by up to 12, and/or C-terminally by up to 8 amino acids.
6. The method of claim 1 , wherein said adhesin is deleted N-terminally by up to 10 or 8, and/or C-terminally by up to 5 amino acids.
7. The method of claim 1 , wherein the adhesin has one or more of the following mutations:
V28W; V28F; A39Q; A39S; I41L; Q47S; Q47T; I85L; T95L; G118S and T123I.
8. The method of claim 1 , wherein the adhesin is used as a contrast agent in identifying bowel cancer in a medical treatment.
9. The method of claim 8 , wherein the contrast agent is directed to CRC cells.