Strategies for N to C solid-phase peptide synthesis
Strategies for N to C solid-phase peptide synthesis
批准号:
10405530
负责人:
Jennifer Lynn Stockdill
金额:
$21.44万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-08-15 至 2023-12-31
关键词:
AddressAmino Acid SequenceAmino AcidsBasic ScienceBiologicalBiological ProcessBiomedical ResearchC-terminalCarboxylic AcidsChemicalsChemistryClinical TrialsComplexConversion disorderCouplingDataDevelopmentDiaminesElementsGene ExpressionGoalsHydrophobicityImprove AccessLassoLinkMediatingMedicalMethodologyMethodsMissionModelingNational Institute of General Medical SciencesPeptide LibraryPeptide SynthesisPeptidesPharmacologic SubstancePhasePlaguePrevalenceProgram DevelopmentPropertyProtocols documentationReactionRecombinantsReportingResearchSchemeSideSolidStudy modelsSulfhydryl CompoundsSulfurTechnologyTemperatureUnited States National Institutes of HealthUreaVertebral columnWorkbasebiological preparationchemical synthesisdesigndiketopiperazineepimerizationfunctional groupimprovedinnovationmicrowave electromagnetic radiationnon-Nativenovelnovel strategiespolypeptidepreventprogramsprotein protein interactionreactivation from latencysynthetic peptidetechnology research and developmenttool
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY
Peptide based pharmaceuticals are becoming increasingly prevalent in late-stage clinical
trials and FDA approvals. Peptide synthesis is traditionally performed in the C to N direction on
solid supports. Peptide synthesis in the N to C direction would enable new opportunities to
improve peptide purity and yield because it will avoid side reactions that plague C to N SPPS
and potentially alter the aggregation state of the peptide during its assembly. However,
challenges such as oxazalone formation and diketopiperazine formation have long prevented
the implementation of such an approach. The long-term objective of this program of research is
to facilitate the synthesis of complex biologically active polypeptides. The objective of this
application is to establish a platform for N to C SPPS that avoids the problematic hurdles of
epimerization caused by oxazalone formation and peptide truncation due to diketopiperazine
formation. We will achieve this objective by employing a mild carbonyl activation strategy that
enable N to C SPPS without causing these undesirable side reactions. We will develop
specialized methods to address slow reactions, challenging sequences, and unique functional
groups that are important to the preparation of biologically active peptides. We will establish the
compatibility of these methods with state-of-the-art SPPS technologies such as microwave and
flow methods. Consistent with the mission of the NIH’s National Institute of General Medical
Sciences, this basic research will ultimately facilitate developments in the study of biological
processes. Furthermore, this research meets the objectives of the Focused Technology
Research and Development Program because the specific aims focus on the technical
challenges and milestones associated with implementing our innovative strategy for peptide
synthesis. If successful, the proposed chemistry will advance biomedical research by positively
impacting all fields where synthetic peptides are needed.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
Facile triflic acid-catalyzed α-1,2-cis-thio glycosylations: scope and application to the synthesis of S-linked oligosaccharides, glycolipids, sublancin glycopeptides, and TN/TF antigens.
简易三氟甲磺酸催化α-1,2-顺式硫代糖基化:S-连接寡糖、糖脂、sublancin 糖肽和 TN/TF 抗原合成的范围和应用。
DOI:
10.1039/c9sc04079j
发表时间:
2019
期刊:
Chemical science
影响因子:
8.4
作者:
[Zhu,Sanyong, Samala,Ganesh, Sletten,EricT, Stockdill,JenniferL, Nguyen,HienM]
通讯作者:
Nguyen,HienM
Strategies for N to C solid-phase peptide synthesis
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批准号:10183269
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项目类别:
-
资助金额:$30.05万
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财政年份:2019
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负责人:Jennifer Lynn Stockdill
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依托单位:
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
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批准号:8534978
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项目类别:
-
资助金额:$24.9万
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财政年份:2011
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负责人:Jennifer Lynn Stockdill
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依托单位:
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
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批准号:8091059
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项目类别:
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资助金额:$9.0万
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财政年份:2011
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负责人:Jennifer Lynn Stockdill
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依托单位:
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
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批准号:8721435
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项目类别:
-
资助金额:$30.42万
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财政年份:2011
-
负责人:Jennifer Lynn Stockdill
-
依托单位:
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
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批准号:8242048
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项目类别:
-
资助金额:$3.0万
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财政年份:2011
-
负责人:Jennifer Lynn Stockdill
-
依托单位:
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
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批准号:8545182
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项目类别:
-
资助金额:$23.71万
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财政年份:2011
-
负责人:Jennifer Lynn Stockdill
-
依托单位:
C-N Bond-Forming Methodologies for the Synthesis of Small Molecules and Peptides
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批准号:8690211
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项目类别:
-
资助金额:$4.64万
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财政年份:2011
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负责人:Jennifer Lynn Stockdill
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依托单位:
Azides as Synthons for Isonitriles: Facilitating Challenging Coupling Reactions
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批准号:7808305
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项目类别:
-
资助金额:$3.04万
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财政年份:2010
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负责人:Jennifer Lynn Stockdill
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依托单位:
海外基金