Sensing of biological molecules using carbon nanotubes as optical labels

• US 20090166560A1
• Filed: 10/24/2007
• Published: 07/02/2009
• Est. Priority Date: 10/26/2006
• Status: Abandoned Application

• Current Assignee: Board of Trustees of the Leland Stanford Junior University (Stanford Management Co.)
• Original Assignee: Board of Trustees of the Leland Stanford Junior University (Stanford Management Co.)
• Inventors: Bangsaruntip, Sarunya, Nakayama, Nozomi, Dai, Hongjie
• Application Number:
  US11/977,550
• Publication Number:
  US 20090166560A1
• Time in Patent Office: Days
• US Class Current: 250/492.100
• CPC Class Codes: B82Y 15/00 Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: B82Y 40/00 Manufacture or treatment of nanostructures
• CPC Class Codes: B82Y 5/00 Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
• CPC Class Codes: C01B 2202/02 Single-walled nanotubes
• CPC Class Codes: C01B 2202/04 Nanotubes with a specific amount of walls
• CPC Class Codes: C01B 2202/06 Multi-walled nanotubes
• CPC Class Codes: C01B 2202/28 Solid content in solvents
• CPC Class Codes: C01B 32/156 After-treatment
• CPC Class Codes: C01B 32/174 Derivatisation; Solubilisation; Dispersion in solvents
• CPC Class Codes: G01N 33/54346 Nanoparticles
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings

Abstract

Disclosed are methods and materials including carbon nanotubes which have a strong Raman and/or fluorescent signal and which have been modified with an amphiphilic molecule having available functional linking groups for linking to a biological compound. Exemplified are surface-functionalized SWNTs (single walled nanotubes) as highly sensitive bio-labels based on the detection of their spectroscopic Raman signature. By solubilizing the nanotubes with polyethylene glycol (PEG)-containing phospholipids, aqueous-stable as well as biocompatible SWNT labels are produced. Specificity in biological detection is then attained by immobilizing reporting molecules off this PEG layer. Highly selective detection of surface immobilized proteins is achieved with detection limit of ˜10 femtomolar, three orders of magnitude higher than the fluorescent technique. Signal stability upon Raman readout as well as compatibility of the SWNT-tagged proteins to the microarray protocols are also demonstrated, making these biocompatible SWNTs highly attractive as novel, alternative bio-labels for ultrasensitive detection of proteins. When excited with a near infrared laser, the nanoparticles give off a distinctive fluorescence signal.

Claims

1. A composition comprising:

a) a carbon nanoparticle;

b) a solubilizing molecule having (i) a hydrophobic portion attached to the carbon nanoparticle and (ii) a hydrophilic portion for solubilizing the composition and having a linking group; and

c) a biological labeling molecule attached to the linking group.

2. The composition of claim 1 where the carbon nanoparticle is a carbon nanotube having predominantly sp2 bonded carbon.

3. The composition of claim 1 where the carbon nanoparticle is an SWNT.

4. The composition of claim 1 where the carbon nanoparticle is an MWNT.

5. The composition of claim 1 where the amphiphilic molecule comprises a phospholipid.

6. The composition of claim 1 where the amphiphilic molecule comprises PEG.

7. The composition of claim 1 where the amphiphilic molecule comprises a hydrophobic portion selected from the group consisting of:

an aromatic compound, an aliphatic compound, and a polycyclic aromatic compound.

8. The composition of claim 7 where the polycyclic aromatic compound is a pyrene.

9. The composition of claim 1 where the amphiphilic molecule comprises a fluorophore adsorbed on the nanoparticle.

10. The composition of claim 9 where the fluorophore is a fluorescein derivative selected from the group consisting of FITC, DTAF and NHS-fluorescein.

11. The composition of claim 10 where the amphiphilic molecule comprises FITC-PEG-NH2.

12. The composition of claim 1 where the biological labeling molecule is selected from the group consisting of proteins and polynucleotides.

13. The composition of claim 11 where the biological labeling molecule is an antibody.

14. A method for preparing a composition for labeling a biological material, comprising the steps of:

(a) obtaining a nanoparticle;

(b) attaching the nanoparticle to a solubilizing molecule having a hydrophilic portion; and

(c) linking a biological labeling molecule to the hydrophilic portion.

15. The method of claim 14 where the nanoparticle is selected from the group consisting of fullerenes, SWNTs, DWNTs and MWNTs.

16. The method of claim 14 where the solubilizing molecule comprises PEG.

17. The method of claim 14 where the PEG is covalently linked to the nanoparticle.

18. The method of claim 14 further comprising the step of adding additional PEG units to the PEG portion.

19. The method of claim 15 where the solubilizing molecule comprises a phospholipid linked to PEG.

20. The method of claim 15 where the biological labeling molecule is an antibody or a polynucleotide.

21. The method of claim 15 where the biological labeling molecule is a thiolated antibody, and comprising the step of linking the thiolated antibody to a bifunctional coupling agent which has been bound to the solubilizing molecule.

22. The method of claim 15 where the nanoparticles is a carbon nanotube.

23. The method of claim 22 where the carbon nanotube is selected from the group consisting of SWNTs, DWNTs and MWNTs.

24. A method of detecting an analyte using Raman scattering with an optical source exciting a sample and an optical detector detecting changes in light scattered by the sample, comprising the step of labeling a portion of the sample with a specific ligand linked to a carbon nanoparticle.

25. The method of claim 24 where the detecting detects a Raman shift around 1550-1600 cm-1.

26. The method of claim 24 where the detecting detects a Raman shift around 0-400 cm-1.

27. The method of claim 24 where the nanoparticle is linked to an amphiphilic molecule.

28. The method of claim 24 where the carbon nanoparticles is an SWNT.

29. The method of claim 24 where the analyte is present in a concentration less than 10 fM.

30. The method of claim 24 where the analyte and ligand is selected from the group consisting of antigen-antibody and nucleic acids and polynucleotides.

31. The method of claim 24 where the step of labeling a portion of the sample with a specific ligand linked to a carbon nanoparticle comprises the step of labeling the sample with a specific ligand linked to a fluorophore and a carbon nanoparticles, and further comprising the step of detecting fluorescence.

32. A method of labeling a cell for detection by fluorescence, comprising the steps of:

a) contacting the cell with a composition comprising

b) a carbon nanoparticle;

c) a solubilizing molecule having a hydrophobic portion attached to the carbon nanoparticle and a hydrophilic portion for solubilizing the composition and having a linking group; and

d) a biological labeling molecule specific for the cell attached to the linking group;

e) forming a complex of the cell and the composition of step (a);

f) irradiating the complex with near infrared light; and

g) detecting near infrared photoluminescence from the carbon nanoparticle.

33. The method of claim 32 where the carbon nanoparticle is a carbon nanotube and the photoluminescence is in the 900-1600 nm region.

34. The method of claim 32 where the irradiating is done with a near infrared laser.

35. The method of claim 34 further comprising the step of measuring Raman scattering.

36. The method of claim 32 where the biological labeling molecule is a monoclonal antibody to a cell surface antigen.

38. A method of detecting analytes in a sample comprising the steps of applying the composition of claim 32 to the analytes, contacting the sample with coherent light, and identifying Raman signals from the sample, where said two different biological labeling molecules produce two different Raman signals upon detection of two different analytes.

37. A composition comprising:

a) at least two different carbon nanoparticles;

b) solubilizing molecules having (i) a hydrophobic portion attached to the carbon nanoparticles and (ii) a hydrophilic portion for solubilizing the composition and having a linking group; and

c) at least two different biological labeling molecule attached to the linking group of respective different nanoparticles.