Related Experiment Video
Updated: Dec 23, 2025

Characterization of MLKL-mediated Plasma Membrane Rupture in Necroptosis
Published on: August 7, 2018
Anti-apoptotic capacity of Mcl-1Δ127
Yong Wang1, Wenhua Su1, Zihao Mai1
1MOE Key Laboratory & Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou, 510631, China.
Abstract:
The anti-apoptotic ability of Mcl-1Δ127, a caspase cleavage product of Mcl-1, is debated. We here used fluorescence imaging to assess the anti-apoptotic capacity of Mcl-1Δ127 in living cells. Fluorescence imaging of living cells expressing CFP-Mcl-1Δ127 showed that Mcl-1Δ127 existed mainly in cytoplasm. Fluorescence imaging of living cells co-expressing CFP-Mcl-1Δ127 and YFP-Bak, CFP-Mcl-1Δ127 and YFP-BimL, CFP-Mcl-1Δ127 and YFP-Puma or CFP-Mcl-1Δ127 and YFP-tBid showed that Mcl-1Δ127 markedly inhibited the oligomerization of Bak, BimL, Puma and tBid on mitochondria and also inhibited the Bak-, BimL-, Puma- or tBid-mediated cell death, resulting in their partial localization in cytoplasm. Fluorescence resonance energy transfer (FRET) imaging proved that Mcl-1Δ127 bound to Bak, BimL, Puma and tBid, respectively. Fluorescence loss in photobleaching (FLIP) analyses showed that Mcl-1Δ127 did prevent Bak oligomerization by retrotranslocating Bak from mitochondria into cytoplasm. Collectively, Mcl-1Δ127 has the same anti-apoptotic capacity as Mcl-1, and prevents apoptosis by sequestering BH3-only or Bak proteins, thus inhibiting their oligomerization on mitochondria.
Insights
Mcl-1Δ127, a Mcl-1 fragment, effectively prevents cell death by binding to pro-apoptotic proteins like Bak. This Mcl-1 fragment sequesters these proteins, inhibiting their mitochondrial activity and apoptosis.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- The anti-apoptotic function of Mcl-1Δ127, a caspase-cleaved fragment of Mcl-1, remains under investigation.
- Understanding Mcl-1Δ127's role is crucial for apoptosis research.
Purpose of the Study:
- To investigate the anti-apoptotic capacity of Mcl-1Δ127 in living cells.
- To elucidate the mechanism by which Mcl-1Δ127 inhibits apoptosis.
Main Methods:
- Utilized fluorescence imaging techniques to observe Mcl-1Δ127 localization and interactions in living cells.
- Employed Förster Resonance Energy Transfer (FRET) and Fluorescence Loss In Photobleaching (FLIP) to analyze protein binding and oligomerization dynamics.
- Assessed the impact of Mcl-1Δ127 on cell death mediated by Bak, BimL, Puma, and tBid.
Main Results:
- Mcl-1Δ127 was primarily localized in the cytoplasm.
- Mcl-1Δ127 significantly inhibited the mitochondrial oligomerization of Bak, BimL, Puma, and tBid.
- Mcl-1Δ127 prevented cell death induced by Bak, BimL, Puma, and tBid, partly by causing their cytoplasmic localization.
- FRET confirmed Mcl-1Δ127 binding to Bak, BimL, Puma, and tBid.
- FLIP demonstrated that Mcl-1Δ127 prevents Bak oligomerization by facilitating Bak retro-translocation from mitochondria to the cytoplasm.
Conclusions:
- Mcl-1Δ127 exhibits anti-apoptotic activity comparable to full-length Mcl-1.
- Mcl-1Δ127 inhibits apoptosis by sequestering BH3-only proteins and Bak, thereby preventing their mitochondrial oligomerization.
Related Concept Videos
The Intrinsic Apoptotic Pathway
The Extrinsic Apoptotic Pathway
Abnormal Proliferation
Apoptosis
Caspases

