Site-selective modification of proteins using cucurbit[7]uril as supramolecular protection for N-terminal aromatic amino acids-Reference-Cited by-同舟云学术

Site-selective modification of proteins using cucurbit[7]uril as supramolecular protection for N-terminal aromatic amino acids

Published:2020 Issue:23 Volume:18 Page:4371-4375
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Smith Anton A. A.¹²³⁴⁵^ORCID,Maikawa Caitlin L.⁶²³⁴^ORCID,Roth Gillie A.⁶²³⁴^ORCID,Appel Eric A.¹²³⁴⁶^ORCID

Affiliation:

1. Department of Materials Science & Engineering

2. Stanford University

3. Stanford

4. USA

5. Department of Chemistry

6. Department of Bioengineering

Abstract

Supramolecular protection of N-terminal aromatic amino acids through complexation with cucurbit[7]uril can enable site-selective protein modification of unfavored motifs.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Novo Nordisk Fonden

Natural Sciences and Engineering Research Council of Canada

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01004A

Reference44 articles.

1. Chemistry for peptide and protein PEGylation

2. PEGylation of therapeutic proteins

3. Targeting the N terminus for site-selective protein modification

4. A general method for highly selective crosslinking of unprotected polypeptides via pH-controlled modification of N-terminal .alpha.-amino groups

5. Glucose-responsive insulin activity by covalent modification with aliphatic phenylboronic acid conjugates

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