Rotaxane probes for protease detection by 129Xe hyperCEST NMR

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Rotaxane probes for protease detection by 129Xe hyperCEST NMR

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NMR processing:

MDD

NMR assignment:

Backbone:

Side-chains:

NOEs:

Structure from NMR restraints:

Ab initio:

Fragment-based:

Rosetta-NMR (Robetta)

Template-based:

GeNMR

I-TASSER

Refinement:

Amber

Structure from chemical shifts:

Fragment-based:

Homology-based:

Torsion angles from chemical shifts:

Preditor

TALOS

Promega- Proline

Secondary structure from chemical shifts:

CSI (via RCI server)

TALOS

MICS caps, β-turns

d2D

PECAN

Flexibility from chemical shifts:

RCI

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HADDOCK

Chemical shifts re-referencing:

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SAVES2 or SAVES4

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V-NMR

Flexibility from structure:

Backbone S2

Methyl S2

B-factor

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Antechamber

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Shiftx2

Sparta+

Camshift

CH3shift- Methyl

ArShift- Aromatic

ShiftS

Proshift

PPM

CheShift-2- Cα

From sequence:

Shifty

Camcoil

Poulsen_rc_CS

Disordered proteins:

MAXOCC

Format conversion & validation:

CCPN

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Validate NMR-STAR 3.1

NMR sample preparation:

Protein disorder:

DisMeta

Protein solubility:

Isotope labeling:

Solid-state NMR:

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05-03-2017, 07:03 PM

nmrlearner

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Rotaxane probes for protease detection by 129Xe hyperCEST NMR

From The DNP-NMR Blog:

Rotaxane probes for protease detection by 129Xe hyperCEST NMR

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Slack, C.C., et al., Rotaxane probes for protease detection by 129Xe hyperCEST NMR. Chem Commun (Camb), 2017. 53(6): p. 1076-1079.

https://www.ncbi.nlm.nih.gov/pubmed/28044166

We report a CB6 rotaxane for the 129Xe hyperCEST NMR detection of matrix metalloprotease 2 (MMP-2) activity. MMP-2 is overexpressed in cancer tissue, and hence is a cancer marker. A peptide containing an MMP-2 recognition sequence was incorporated into the rotaxane, synthesized via CB6-promoted click chemistry. Upon cleavage of the rotaxane by MMP-2, CB6 became accessible for 129Xe@CB6 interactions, leading to protease-responsive hyperCEST activation.

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