Abstract
Cellular lipid bilayers are critical platforms for the myriad of functions performed by membrane proteins. Drugs modified with lipid membrane anchors can selectively target membrane proteins. In this review, we discuss preferences of representative lipidated molecules for specific cellular membrane domains and the recent progress in lipidated drug delivery.
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Abbreviations
- ER:
-
Endoplasmic reticulum
- GPI:
-
Glycosylphosphatidylinositol
- PEG:
-
Polyethylene glycol
- CLIC:
-
Clathrin-independent carrier
- GPCR:
-
G protein-coupled receptor
- APP:
-
Amyloid precursor protein
- HIV:
-
Human immunodeficiency virus
- HBV:
-
Hepatitis B virus
- PAR1:
-
Protease-activated receptor 1
- CXCR4:
-
CXC-type receptor 4
- SMO:
-
Smoothened
- IGF1R:
-
Insulin-like growth factor 1 receptor
- STAT3:
-
Signal transducer and activator of transcription 3
- SH2:
-
Src homology 2
- TRPV1:
-
Transient receptor potential vanilloid 1
- PAT:
-
Palmitoyl acyl transferase
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Mori, T., Katayama, Y. (2014). Membrane-Domain-Selective Drug Targeting Based on Lipid Modification. In: Prokop, A., Iwasaki, Y., Harada, A. (eds) Intracellular Delivery II. Fundamental Biomedical Technologies, vol 7. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-8896-0_11
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DOI: https://doi.org/10.1007/978-94-017-8896-0_11
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