O -octadecylhydroxylamine

O -octadecylhydroxylamine
Имена
	Имя IUPAC O -octadecylhydroxylamine
	Другие имена 1- (Aminooxy) Octadecane ;
Идентификаторы
3D model ( JSmol )	Интерактивное изображение ;
Chemspider	292737 ;
PubChem CID	330458 ;
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	показывать Улыбается
Характеристики
Химическая формула	C 18 H 39 N O
Молярная масса	285.516 g/mol
Появление	Пушистый белый твердый
Density	0.9±0.1 g/cm3
log P	8.307
Vapor pressure	0.0±0.9 mmHg (25 °C);
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

O -octadecydhydroxylamine ( ODHA ) представляет собой белое твердое органическое соединение с формулой C ₁₈ H ₃₉ Нет . ODHA является неканоническим липидом , который содержит насыщенный алкильный хвост и аминооокси головную группу. Этот неканонический липид может быть выборочно добавлен к N-конце желаемых биополимеров, таких как пептиды. ODHA управляет супрамолекулярной сборкой модифицированного белка , предположительно, через гидрофобный коллапс цепей ODHA. ^{[ 1 ]}^{[ 2 ]}^{[ 3 ]}^{[ 4 ]}^{[ 5 ]}

Подготовка

ODHA готовится из реакции между 2- (октадецилокси) изоиндолин-1,3-дионовой гидрата и гидразин . ^{[ 1 ]}^{[ 6 ]}

Реакция

Модификация ODHA

A pH-responsive oxime bond is used to install an ODHA-type synthetic lipid (octadecylhydroxylamine) in place of the N terminal serine residue in N-myristoylation PTM. N-terminal myristoylation is a post-translational modification carried out by the enzyme N-myristoyltransferase. Generally, the 12-carbon myristoyl lipid is added to the N-terminus of proteins. The lipid is attached to the protein via a stable amide bond. However, the ODHA lipid is attached to the protein via an oxime bond, due to the structure of the non-canonical lipid. The reaction is chemical, compared to the enzymatic NMT reaction. Self-assembly is driven by the hydrophobic nature of the attached lipid, and disassembly is controlled by oxime degradation in an acidic environment. The reaction between the lipid and oxidized protein is biomolecular, which means it is following second order rate kinetics since it is dependent on oxidized protein (ELP) and lipids (ODHA).^[1]^[6]^[7]

{d[ODHA-ELP] \over dt}=K[ELP][ODHA]

References

^ Jump up to: ^a ^b ^c Scheibel, Dieter M.; Hossain, Md. Shahadat; Smith, Amy L.; Lynch, Christopher J.; Mozhdehi, Davoud (2020-03-17). "Post-Translational Modification Mimicry for Programmable Assembly of Elastin-Based Protein Polymers". ACS Macro Letters. 9 (3): 371–376. doi:10.1021/acsmacrolett.0c00041. ISSN 2161-1653. PMID 35648543. S2CID 213897356.
^ PubChem. "O-octadecylhydroxylamine". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-11-19.
^ Takahara, M.; Wakabayashi, R.; Minamihata, K.; Goto, M.; Kamiya, N. Design of Lipid−Protein Conjugates Using Amphiphilic Peptide Substrates of Microbial Transglutaminase. ACS Appl. Bio Mater. 2018, 1 (6), 1823−182
^ Lipid Modification of Proteins through Sortase-Catalyzed Transpeptidation. J. Am. Chem. Soc. 2008, 130 (48), 16338−16343
^ Takahara, M.; Wakabayashi, R.; Fujimoto, N.; Minamihata, K.; Goto, M.; Kamiya, N. Enzymatic Cell-Surface Decoration with Proteins Using Amphiphilic Lipid-Fused Peptide Substrates. Chem. - Eur. J. 2019, 25 (30), 7315−7321
^ Jump up to: ^a ^b Tirelli, Nicola; Amabile, Stefania; Cellai, Caterina; Pucci, Andrea; Regoli, Leonardo; Ruggeri, Giacomo; Ciardelli, Francesco (2001-02-28). "New Terthiophene Derivatives for Ultrahigh Molecular Weight Polyethylene-Based Absorption Polarizers". Macromolecules. 34 (7): 2129–2137. Bibcode:2001MaMol..34.2129T. doi:10.1021/ma001518q. ISSN 0024-9297.
^ Spears, Richard J.; Fascione, Martin A. (2016). "Site-selective incorporation and ligation of protein aldehydes". Organic & Biomolecular Chemistry. 14 (32): 7622–7638. doi:10.1039/c6ob00778c. ISSN 1477-0520. PMID 27381815. S2CID 5019789.

[:0-1] Jump up to: ^a ^b ^c Scheibel, Dieter M.; Hossain, Md. Shahadat; Smith, Amy L.; Lynch, Christopher J.; Mozhdehi, Davoud (2020-03-17). "Post-Translational Modification Mimicry for Programmable Assembly of Elastin-Based Protein Polymers". ACS Macro Letters. 9 (3): 371–376. doi:10.1021/acsmacrolett.0c00041. ISSN 2161-1653. PMID 35648543. S2CID 213897356.

[2] PubChem. "O-octadecylhydroxylamine". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-11-19.

[3] Takahara, M.; Wakabayashi, R.; Minamihata, K.; Goto, M.; Kamiya, N. Design of Lipid−Protein Conjugates Using Amphiphilic Peptide Substrates of Microbial Transglutaminase. ACS Appl. Bio Mater. 2018, 1 (6), 1823−182

[4] Lipid Modification of Proteins through Sortase-Catalyzed Transpeptidation. J. Am. Chem. Soc. 2008, 130 (48), 16338−16343

[5] Takahara, M.; Wakabayashi, R.; Fujimoto, N.; Minamihata, K.; Goto, M.; Kamiya, N. Enzymatic Cell-Surface Decoration with Proteins Using Amphiphilic Lipid-Fused Peptide Substrates. Chem. - Eur. J. 2019, 25 (30), 7315−7321

[:1-6] Jump up to: ^a ^b Tirelli, Nicola; Amabile, Stefania; Cellai, Caterina; Pucci, Andrea; Regoli, Leonardo; Ruggeri, Giacomo; Ciardelli, Francesco (2001-02-28). "New Terthiophene Derivatives for Ultrahigh Molecular Weight Polyethylene-Based Absorption Polarizers". Macromolecules. 34 (7): 2129–2137. Bibcode:2001MaMol..34.2129T. doi:10.1021/ma001518q. ISSN 0024-9297.

[7] Spears, Richard J.; Fascione, Martin A. (2016). "Site-selective incorporation and ligation of protein aldehydes". Organic & Biomolecular Chemistry. 14 (32): 7622–7638. doi:10.1039/c6ob00778c. ISSN 1477-0520. PMID 27381815. S2CID 5019789.

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