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Merck
모든 사진(1)

주요 문서

5.00527

Sigma-Aldrich

APETx2, Anthopleura elegantissima, Recombinant, E. coli

recombinant, expressed in E. coli

동의어(들):

APETx2, Anthopleura elegantissima, Recombinant, E. coli, Acid-Sensing Ion Channel 3 Blocker, ASIC3 Channel Blocker

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About This Item

실험식(Hill 표기법):
C196H280N54O61S6
CAS Number:
Molecular Weight:
4561.04
UNSPSC 코드:
12352200
가격 및 재고 정보를 현재 이용할 수 없음

재조합

expressed in E. coli

Quality Level

분석

≥95% (HPLC)

양식

lyophilized powder

효능

63 nM IC50

제조업체/상표

Calbiochem®

저장 조건

OK to freeze
protect from light

solubility

aqueous buffer: soluble

저장 온도

−20°C

일반 설명

Originally isolated from sea anemone Anthopleura elegantissima, the 42 amino-acid toxin APETx2 is shown to block acidification-induced activation of homotrimeric acid-sensing ion channel composed of rat or human ASIC3 (IC50 against pH 7.4 to 6 ramping-induced transient current = 63 nM and 175 nM by whole-cell patch-clamp using COS cells expressing respective channel), but not rat ASIC1a, ASIC1b, or ASIC2a, in a reversible manner, presumably via its N-terminus interaction with type I β turn that connects β-strands I&II in the ASIC3 extracellular β-ball region. In addition to acidification-induced classical transient current, APETx2 is also shown to inhibit the Na+-dependent, alkalization-induced nonconventional channel activity seen in human, but not rat, ASIC3 (complete inhibition by 1 µM APETx3; pH 8.0). APETx2 in vivo efficacy is demonstrated in various rat pain induction models, including acid- (via calf i.m. injection of 100 µL pH 4.0 saline on day 1&5) induced mechanical hypersensitivity (pain withdrawal threshold = 76% and 24% of control rats with or without 100 µL 2.2 µM APETx2 i.m. injection prior to the second pH 4.0 saline injection). Although structurally related to known K+ channel modulators APETx1 and BDS-1/II, APETx2 is reported to display much reduced potency against Kv3.4 (38% inhibition by 3 µM APETx2) and little or no effect toward hERG, Kv2.2, Kv3.1, Kv4.2, or Kv4.3 channel activity.
Originally isolated from sea anemone Anthopleura elegantissima, the 42 amino-acid toxin APETx2 is shown to block acidification-induced activation of homotrimeric acid-sensing ion channel composed of rat or human ASIC3, but not rat ASIC1a, ASIC1b, or ASIC2a, in a reversible manner. APETx2 is also shown to inhibit the Na+-dependent, alkalization-induced "nonconventional" channel activity seen in human, but not rat, ASIC3. APETx2 in vivo efficacy is demonstrated in various rat pain induction models (100 µL 2.2 µM APETx2 via i.m. injection). Reported to display much reduced potency against Kv3.4 and little or no effect toward hERG, Kv2.2, Kv3.1, Kv4.2, or Kv4.3 channel activity.

생화학적/생리학적 작용

Primary Target
ASIC3
Reversible: yes

경고

Toxicity: Standard Handling (A)

서열

H-Gly-Thr-Ala-Cys⁴-Ser-Cys⁶-Gly-Asn-Ser-Lys-Gly-Ile-Tyr-Trp-Phe-Tyr-Arg-Pro-Ser-Cys²⁰-Pro-Thr-Asp-Arg-Gly-Tyr-Thr-Gly-Ser-Cys³⁰-Arg-Tyr-Phe-Leu-Gly-Thr-Cys³⁷-Cys³⁸-Thr-Pro-Ala-Asp-OH (disulfide bonds: 4 → 37, 6 → 30, 20 → 38)

물리적 형태

Supplied as a trifluoroacetate salt.

재구성

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

기타 정보

Delaunay, A., et al. 2012. Proc. Natl. Acad. Sci.109, 13124.
Sherwood, T.W., et al. 2012. Am. J. Physiol. Cell Physiol.303, C699.
Karczewski, J., et al. 2010. Br J Pharmacol.161, 950.
Chagot, B., et al. 2005. Protein Sci.14, 2003.

Diochot, S., et al. 2004. EMBO J.23, 1516.

법적 정보

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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