专肽生物_定制多肽合成服务_多肽合成定制服务_多肽合成厂家_多肽合成公司

Proadrenomedullin (1-20), human 是一种有效的降压和儿茶酚胺释放抑制肽，由嗜铬细胞释放，其抑制 PC12 嗜铬细胞瘤细胞儿茶酚胺分泌，IC50 值约为 ~350 nM，并以非竞争性的方式特别作用于烟碱胆碱能受体。
Proadrenomedullin (1-20), human is a potent hypotensive and catecholamine release–inhibitory peptide released from chromaffin cells with an IC50 of ~350 nM for catecholamine secretion in PC12 pheochromocytoma cells, acting in a noncompetitive manner specifically at the nicotinic cholinergic receptor[1].

PAMP (human) is a peptide that binds to the G-protein coupled receptor, M3. It activates the ion channel and induces an influx of calcium ions into cells. This can lead to cell proliferation and differentiation, as well as increased blood flow in the brain. PAMP has been shown to inhibit ligand-induced activation of M3 receptors by competing with the natural ligands for binding sites on these receptors. It has also been shown to have high purity (>95%), and is currently under research for its use in various medical applications such as cancer therapy, pain management, and treatment of respiratory diseases.

Definition
Adrenomedullin (AM) is a pluripotent peptide and a hypotensive substance extracted from human adrenal tumour. Due to its origin of discovery, i.e. the medulla of the adrenal gland, the peptide is named adrenomedullin.
Discovery
AM was initially isolated from phaechromcytoma cells in 1993 by Kitmura K and his associates1.

Classification
AM is a member of the calcitonin family of peptides. In teleost fish, AM forms an independent subfamily consisting of five members viz. (AM1–AM5). This teleost AM family comprises three groups, AM1/AM4, AM2/AM3, and AM5 2,3.

Structural Characteristics
The peptide consists of 52 amino acids with a 6-member ring structure linked by a disulfide bond between amino acid 16 and 21 and amidated-COOH terminal4. It has 27 % homology with the calcitonin gene-related peptide (CGRP).

Mechanism of action
AM peptides act through specific receptors in the plasma membrane to activate adenylate cyclase activity and modulate Ca2+ flux in the target cells. The intracellular free Ca2+ increases on the activation of phospholipase C and formation of inositol 1, 4, 5-trisphosphate in the endothelial cells. The intracellular increase of Ca2+ activates endothelial nitric oxide synthase which leads to vascular relaxation5.

Function
AM is the most potent endogenous vasodilatory peptide found in the body6. They increase the tolerance of cells to oxidative stress, hypoxic injury and angiogenesis. It plays an important role in neurotransmission and ovarian function and in kidney, it acts as a diuretic and natriuretic7. AM is considered to play an important endocrine role in various tissues in maintaining electrolyte and fluid homeostasis8. It is used in the diagnosis and treatment of preeclampsia, type II diabetic patients and to promote fetal growth. They also play an important role in the regulation of insulin secretion and blood glucose metabolism.

References

1.     Kitamura K, Kangawa K, Kawamoto M, Ichiki Y, Nakamura S, Matsuo H, Eto T (1993). Adrenomedullin: a novel hypotensive peptide isolated from human pheochromocytoma. Biochem Biophys Res Commun., 192 (2):553-560.

2.     Ogoshi M, Nobata S, and Takei Y (2008). Potent osmoregulatory actions of homologous adrenomedullins administered peripherally and centrally in eels. Am J Physiol Regul Integr Comp Physiol, 295: 2075-2083.

3.     Ogoshi M, Inoue K, Naruse K, Takei Y (2006). Evolutionary history of the calcitonin gene-related peptide family in vertebrates revealed by comparative genomic analyses. Peptides, 27 (12):3154-3164.

4.     Cockcroft JR, Noon JP, Gardner-Medwin J, Bennett T (1997). Haemodynamic effects of adrenomedullin in human resistance and capacitance vessels. Br J Clin Pharmacol, 44(1):57-60.

5.     Shimekake Y, Nagata K, Ohta S, Kambayashi Y, Teraoka H, Kitamura K, Eto T, Kangawa K, Matsuo H (1995). Adrenomedullin stimulates two signal transduction pathways, cAMP accumulation and Ca2+ mobilization, in bovine aortic endothelial cells. J Biol Chem, 270: 4412-4417.

6.     Yanagawa B, Nagaya N (2007). Adrenomedullin: molecular mechanisms and its role in cardiac disease. Amino Acids, 32 (1):157-164.

7.     Vesely DL (2003). Natriuretic peptides and acute renal failure. Am J Physiol Renal Physiol, 285 (2):167-177.

8.     Ruzicska E, Toth M, Tulassay Z, Somogyi A (2001). Adrenomedullin and diabetes mellitus. Diabetes Metab Res Rev, 17 (5):321-329.

多肽H2N-Ala-Arg-Leu-Asp-Val-Ala-Ser-Glu-Phe-Arg-Lys-Lys-Trp-Asn-Lys-Trp-Ala-Leu-Ser-Arg-NH2的合成步骤：

1、合成MBHA树脂：取若干克的MBHA树脂（如初始取代度为0.5mmol/g）和1倍树脂摩尔量的Fmoc-Linker-OH加入到反应器中，加入DMF，搅拌使氨基酸完全溶解。再加入树脂2倍量的DIEPA，搅拌混合均匀。再加入树脂0.95倍量的HBTU，搅拌混合均匀。反应3-4小时后，用DMF洗涤3次。用2倍树脂体积的10%乙酸酐/DMF 进行封端30分钟。然后再用DMF洗涤3次，甲醇洗涤2次，DCM洗涤2次，再用甲醇洗涤2次。真空干燥12小时以上，得到干燥的树脂{Fmoc-Linker-MHBA Resin}，测定取代度。这里测得取代度为 0.3mmol/g。结构如下图：

2、脱Fmoc：取1.45g的上述树脂，用DCM或DMF溶胀20分钟。用DMF洗涤2遍。加3倍树脂体积的20%Pip/DMF溶液，鼓氮气30分钟，然后2倍树脂体积的DMF 洗涤5次。得到 H2N-Linker-MBHA Resin 。（此步骤脱除Fmoc基团，茚三酮检测为蓝色，Pip为哌啶）。结构图如下：

3、缩合：取1.3mmol Fmoc-Arg(Pbf)-OH 氨基酸，加入到上述树脂里，加适当DMF溶解氨基酸，再依次加入2.61mmol DIPEA，1.24mmol HBTU。反应30分钟后，取小样洗涤，茚三酮检测为无色。用2倍树脂体积的DMF 洗涤3次树脂。（洗涤树脂，去掉残留溶剂，为下一步反应做准备）。得到Fmoc-Arg(Pbf)-Linker-MBHA Resin。氨基酸：DIPEA：HBTU：树脂=3：6：2.85：1（摩尔比）。结构图如下：

4、依次循环步骤二、步骤三，依次得到

H2N-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Leu-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Leu-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Arg(Pbf)-Leu-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

H2N-Arg(Pbf)-Leu-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

Fmoc-Ala-Arg(Pbf)-Leu-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin

以上中间结构，均可在专肽生物多肽计算器-多肽结构计算器中，一键画出。

最后再经过步骤二得到 H2N-Ala-Arg(Pbf)-Leu-Asp(OtBu)-Val-Ala-Ser(tBu)-Glu(OtBu)-Phe-Arg(Pbf)-Lys(Boc)-Lys(Boc)-Trp(Boc)-Asn(Trt)-Lys(Boc)-Trp(Boc)-Ala-Leu-Ser(tBu)-Arg(Pbf)-Linker-MBHA Resin，结构如下：

5、切割：6倍树脂体积的切割液（或每1g树脂加8ml左右的切割液），摇床摇晃 2小时，过滤掉树脂，用冰无水乙醚沉淀滤液，并用冰无水乙醚洗涤沉淀物3次，最后将沉淀物放真空干燥釜中，常温干燥24小试，得到粗品H2N-Ala-Arg-Leu-Asp-Val-Ala-Ser-Glu-Phe-Arg-Lys-Lys-Trp-Asn-Lys-Trp-Ala-Leu-Ser-Arg-NH2。结构图见产品结构图。

切割液选择：1）TFA：H2O=95%：5%

2）TFA：H2O：TIS=95%：2.5%：2.5%

3）三氟乙酸：茴香硫醚：1，2-乙二硫醇：苯酚：水=87.5%：5%：2.5%：2.5%：2.5%

（前两种适合没有容易氧化的氨基酸，例如Trp、Cys、Met。第三种适合几乎所有的序列。）

6、纯化冻干：使用液相色谱纯化，收集目标峰液体，进行冻干，获得蓬松的粉末状固体多肽。不过这时要取小样复测下纯度 是否目标纯度。

7、最后总结：

杭州专肽生物技术有限公司（ALLPEPTIDE https://www.allpeptide.com）主营定制多肽合成业务，提供各类长肽，短肽，环肽，提供各类修饰肽，如：荧光标记修饰（CY3、CY5、CY5.5、CY7、FAM、FITC、Rhodamine B、TAMRA等），功能基团修饰肽（叠氮、炔基、DBCO、DOTA、NOTA等），同位素标记肽（N15、C13），订书肽（Stapled Peptide）,脂肪酸修饰肽（Pal、Myr、Ste），磷酸化修饰肽（P-Ser、P-Thr、P-Tyr），环肽（酰胺键环肽、一对或者多对二硫键环），生物素标记肽，PEG修饰肽，甲基化修饰肽等。

以上所有内容，为专肽生物原创内容，请勿发布到其他网站上。