
科生景肽 专利/文献
KS-V Peptide

专利文献 PATENT LITERATURE
-
Chemical synthesis of membrane proteins by the removable backbone modification method.
○ 2017.03 Chemical synthesis of membrane proteins by the removable backbone modification method. -
Chemical synthesis of proteins using peptide hydrazides as thioester surrogates
○ 2013.12 Chemical synthesis of proteins using peptide hydrazides as thioester surrogates -
Ion channel modulation by scorpion hemolymph and its defensin ingredients highlights origin of neurotoxins in telson formed in Paleozoic scorpions.
○ 2020.01 Ion channel modulation by scorpion hemolymph and its defensin ingredients highlights origin of neurotoxins in telson formed in Paleozoic scorpions. -
Chemical Synthesis of Native S-Palmitoylated Membrane Proteins through Removable-Backbone-Modification-Assisted Ser/Thr Ligation.
○ 2020.02 Chemical Synthesis of Native S-Palmitoylated Membrane Proteins through Removable-Backbone-Modification-Assisted Ser/Thr Ligation. -
The New Salicylaldehyde S,S-Propanedithioacetal Ester Enables N-to-C Sequential Native Chemical Ligation and Ser/Thr Ligation for Chemical Protein Synthesis.
○ 2020.04 The New Salicylaldehyde S,S-Propanedithioacetal Ester Enables N-to-C Sequential Native Chemical Ligation and Ser/Thr Ligation for Chemical Protein Synthesis. -
Synthesis of Disulfide Surrogate Peptides Incorporating Large-Span Surrogate Bridges Through a Native-Chemical-Ligation-Assisted Diaminodiacid Strategy.
○ 2020.03 Synthesis of Disulfide Surrogate Peptides Incorporating Large-Span Surrogate Bridges Through a Native-Chemical-Ligation-Assisted Diaminodiacid Strategy. -
A genetically encoded small-size fluorescent pair reveals allosteric conformational changes of G proteins upon its interaction with GPCRs by fluorescence lifetime based FRET.
○ 2020.06 A genetically encoded small-size fluorescent pair reveals allosteric conformational changes of G proteins upon its interaction with GPCRs by fluorescence lifetime based FRET. -
Single-particle cryo-EM structural studies of the β2AR-Gs complex bound with a full agonist formoterol.
○ 2020.07 Single-particle cryo-EM structural studies of the β2AR-Gs complex bound with a full agonist formoterol. -
Cryo-EM structure of trimeric Mycobacterium smegmatis succinate dehydrogenase with a membrane-anchor SdhF.
○ 2020.08 Cryo-EM structure of trimeric Mycobacterium smegmatis succinate dehydrogenase with a membrane-anchor SdhF. -
Cryo-EM structure of the hyperpolarization-activated inwardly rectifying potassium channel KAT1 from Arabidopsis.
○ 2020.09 Cryo-EM structure of the hyperpolarization-activated inwardly rectifying potassium channel KAT1 from Arabidopsis. -
Structural insights into human acid-sensing ion channel 1a inhibition by snake toxin mambalgin1.
○ 2020.09 Structural insights into human acid-sensing ion channel 1a inhibition by snake toxin mambalgin1. -
Chemical synthesis of di-ubiquitin modified histones for further biochemical studies.
○ 2020.05 Chemical synthesis of di-ubiquitin modified histones for further biochemical studies. -
Secondary structure and transmembrane topology analysis of the N-terminal domain of the inner membrane protein EccE1 from M. smegmatis using site-directed spin labeling EPR.
○ 2020.11 Secondary structure and transmembrane topology analysis of the N-terminal domain of the inner membrane protein EccE1 from M. smegmatis using site-directed spin labeling EPR. -
Structural mechanism of cooperative activation of the human calcium-sensing receptor by Ca2+ ions and L-tryptophan.
○ 2021.02 Structural mechanism of cooperative activation of the human calcium-sensing receptor by Ca2+ ions and L-tryptophan. -
Architecture of the mycobacterial succinate dehydrogenase with a membrane-embedded Rieske FeS cluster.
○ 2021.04 Architecture of the mycobacterial succinate dehydrogenase with a membrane-embedded Rieske FeS cluster. -
Structural basis of human α7 nicotinic acetylcholine receptor activation.
○ 2021.05 Structural basis of human α7 nicotinic acetylcholine receptor activation. -
Identification and architecture of a putative secretion tube across mycobacterial outer envelope.
○ 2021.08 Identification and architecture of a putative secretion tube across mycobacterial outer envelope. -
Dipolar coupling-based electron paramagnetic resonance method for protease enzymatic characterization and inhibitor screening.
○ 2021.09 Dipolar coupling-based electron paramagnetic resonance method for protease enzymatic characterization and inhibitor screening. -
Structures of wild-type and H451N mutant human lymphocyte potassium channel KV1.3.
○ 2021.06 Structures of wild-type and H451N mutant human lymphocyte potassium channel KV1.3.
合肥科生景肽生物科技有限公司
地址:安徽省合肥市高新区望江西路5089号中
科大先研院智源楼
电话:0551-65120828 0551-65120826
邮箱:sales@difficultpeptide.com
合肥科生景肽生物科技有限公司
地址:安徽省合肥市高新区望江西路5089号中
科大先研院智源楼
电话:0551-65120828 0551-65120826
邮箱:sales@difficultpeptide.com
在线留言
客户留言
描述: