TIMM23 — Translocase of Inner Mitochondrial Membrane 23

TIMM23 — Translocase of Inner Mitochondrial Membrane 23

Introduction

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TIMM23 — Translocase of Inner Mitochondrial Membrane 23</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>TIMM23</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Translocase of Inner Mitochondrial Membrane 23</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>10q11.21</td>
</tr>
<tr>
<td class="label">NCBI Gene</td>
<td>10098</td>
</tr>
<tr>
<td class="label">Ensembl</td>
<td>ENSG00000132268</td>
</tr>
<tr>
<td class="label">UniProt</td>
<td>O00231</td>
</tr>
<tr>
<td class="label">Diseases</td>
<td>Parkinson's Disease, ALS, Mitochondrial Disorders</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>High in brain, heart, muscle, kidney</td>
</tr>
<tr>
<td class="label">Partner Protein</td>
<td>Function</td>
</tr>
<tr>
<td class="label">TIMM17A/B</td>
<td>Regulatory subunit, controls channel activity</td>
</tr>
<tr>
<td class="label">TIMM44</td>
<td>Motor attachment, recruits mtHsp70</td>
</tr>
<tr>
<td class="label">TIMM50</td>
<td>Inner membrane protein, facilitates transfer</td>
</tr>
<tr>
<td class="label">TIMM22</td>
<td>Minor translocase, involved in carrier protein import</td>
</tr>
<tr>
<td class="label">mtHsp70</td>
<td>Motor protein, provides energy for translocation</td>
</tr>
<tr>
<td class=

TIMM23 — Translocase of Inner Mitochondrial Membrane 23

Introduction

<table class="infobox infobox-gene">
<tr>
<th class="infobox-header" colspan="2">TIMM23 — Translocase of Inner Mitochondrial Membrane 23</th>
</tr>
<tr>
<td class="label">Symbol</td>
<td>TIMM23</td>
</tr>
<tr>
<td class="label">Full Name</td>
<td>Translocase of Inner Mitochondrial Membrane 23</td>
</tr>
<tr>
<td class="label">Chromosome</td>
<td>10q11.21</td>
</tr>
<tr>
<td class="label">NCBI Gene</td>
<td>10098</td>
</tr>
<tr>
<td class="label">Ensembl</td>
<td>ENSG00000132268</td>
</tr>
<tr>
<td class="label">UniProt</td>
<td>O00231</td>
</tr>
<tr>
<td class="label">Diseases</td>
<td>Parkinson's Disease, ALS, Mitochondrial Disorders</td>
</tr>
<tr>
<td class="label">Expression</td>
<td>High in brain, heart, muscle, kidney</td>
</tr>
<tr>
<td class="label">Partner Protein</td>
<td>Function</td>
</tr>
<tr>
<td class="label">TIMM17A/B</td>
<td>Regulatory subunit, controls channel activity</td>
</tr>
<tr>
<td class="label">TIMM44</td>
<td>Motor attachment, recruits mtHsp70</td>
</tr>
<tr>
<td class="label">TIMM50</td>
<td>Inner membrane protein, facilitates transfer</td>
</tr>
<tr>
<td class="label">TIMM22</td>
<td>Minor translocase, involved in carrier protein import</td>
</tr>
<tr>
<td class="label">mtHsp70</td>
<td>Motor protein, provides energy for translocation</td>
</tr>
<tr>
<td class="label">TOM complex</td>
<td>Upperstream import, outer membrane translocase</td>
</tr>
<tr>
<td class="label">OXA1</td>
<td>Insertion of inner membrane proteins</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/heart-failure" style="color:#ef9a9a">Heart Failure</a>, <a href="/wiki/ms" style="color:#ef9a9a">Ms</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">56 edges</a></td>
</tr>
</table>

TIMM23 (Translocase of Inner Mitochondrial Membrane 23) is a critical protein encoded by the TIMM23 gene located on chromosome 10q11.21. This gene, catalogued as NCBI Gene ID 10098 and Ensembl ID ENSG00000132268, encodes a core component of the mitochondrial inner membrane translocase complex (TIM23 complex) [1]. TIMM23 serves as the central channel through which precursor proteins are imported from the cytosol into the mitochondrial matrix or inner membrane, making it essential for mitochondrial function and cellular survival [2]. The protein is highly expressed in energy-demanding tissues, including the brain, heart, skeletal muscle, and kidney, reflecting the high mitochondrial density and energy requirements in these tissues [3].

Mitochondria are essential organelles responsible for ATP production through oxidative phosphorylation, calcium homeostasis, and programmed cell death regulation. Because mitochondria contain their own genome but import hundreds of nuclear-encoded proteins, the mitochondrial protein import machinery—including the TIM23 complex—is fundamentally important for mitochondrial biogenesis and function [4]. Dysfunction of this import system has been increasingly recognized as a contributing factor in neurodegenerative diseases, metabolic disorders, and aging-related pathologies [5].

Overview

Function

Mitochondrial Protein Import

TIMM23 functions as the central pore-forming subunit of the TIM23 complex, which is responsible for the translocation of precursor proteins synthesized in the cytosol into the mitochondrial matrix or inner membrane [6]. The TIM23 complex operates in conjunction with the TOM (Translocase of Outer Mitochondrial Membrane) complex, which recognizes and imports precursor proteins across the outer membrane. After passing through the TOM complex, precursor proteins are delivered to the TIM23 complex for translocation across the inner membrane [7].

The mechanism of protein import through TIM23 involves several steps:

Role in Protein Insertion into the Inner Membrane

Beyond matrix translocation, TIMM23 also facilitates the insertion of integral proteins into the inner membrane through a lateral gating mechanism. This process allows hydrophobic membrane proteins to exit the translocation channel directly into the lipid bilayer of the inner membrane [12]. The TIM23 complex can thus handle both soluble proteins destined for the matrix and hydrophobic proteins that become embedded in the inner membrane.

Structure

The TIMM23 protein is approximately 222 amino acids in length and contains multiple transmembrane helices that anchor it within the inner mitochondrial membrane [13]. Structural studies have revealed that TIMM23 forms a voltage-gated channel that can open and close in response to changes in membrane potential [14]. The protein interacts with TIMM17, which serves as a regulatory component controlling the channel's activity, and with TIMM44, which links the complex to the mitochondrial Hsp70 motor (mtHsp70) for ATP-dependent translocation [15].

The TIM23 complex can be conceptually divided into three functional modules:

• The channel module: TIMM23 forms the central pore
• The regulatory module: TIMM17 modulates channel activity
• The motor module: TIMM44 and mtHsp70 drive translocation

Role in Neurodegenerative Diseases

Parkinson's Disease

TIMM23 has been implicated in the pathogenesis of Parkinson's disease (PD), a progressive neurodegenerative disorder characterized by the loss of dopaminergic [neurons](/entities/neurons) in the substantia nigra [17]. Mitochondrial dysfunction is a central feature of PD, and deficits in mitochondrial protein import have been observed in both familial and sporadic forms of the disease [18].

Research has shown that:

• Mutations in PARK2 (parkin) and PINK1, which are linked to familial PD, affect mitochondrial quality control mechanisms that involve TIMM23 function [19]
• Impairment of the TIM23 complex can lead to mitochondrial respiratory chain defects, increasing susceptibility to neuronal death [20]
• Studies in cellular models have demonstrated that reduced TIMM23 expression compromises mitochondrial function and promotes [apoptosis](/entities/apoptosis) in dopaminergic neurons [21]

Amyotrophic Lateral Sclerosis (ALS)

Amyotrophic lateral sclerosis is a fatal neurodegenerative disease affecting motor neurons. Evidence suggests that mitochondrial dysfunction, including impaired protein import, contributes to motor neuron degeneration in ALS [22].

Key findings linking TIMM23 to ALS include:

• Mitochondria in ALS patients and animal models show reduced protein import capacity [23]
• Mutations in genes encoding mitochondrial proteins, including components of the TIM complex, have been identified in some ALS cases [24]
• Dysregulation of mitochondrial protein import may exacerbate oxidative stress and energy deficits in motor neurons [25]

Mitochondrial Disorders

Primary mitochondrial disorders encompass a group of genetic conditions caused by mutations in mitochondrial or nuclear DNA-encoded proteins that impair mitochondrial function [26]. TIMM23 dysfunction can contribute to these disorders by compromising the import of essential mitochondrial proteins, leading to:

• Reduced oxidative phosphorylation capacity
• Impaired mitochondrial dynamics (fusion/fission)
• Increased susceptibility to metabolic stress

Interactions and Complex Partners

TIMM23 interacts with several other proteins within the mitochondrial import machinery:

These interactions form an interconnected network that ensures efficient and regulated protein import into mitochondria [28].

Clinical Significance

The importance of TIMM23 for cellular survival is underscored by the fact that complete loss of TIMM23 function is embryonic lethal in mice, while partial deficiency leads to mitochondrial dysfunction and increased apoptosis [29]. In humans, variants in the TIMM23 gene have been associated with:

• Early-onset Parkinson's disease [30]
• Peripheral neuropathy [31]
• Metabolic syndrome [32]

• Genetic testing for TIMM23 mutations
• Functional assessment of mitochondrial respiration
• Protein import assays in patient-derived cells

Research and Therapeutic Implications

Understanding TIMM23 function has inspired therapeutic strategies aimed at enhancing mitochondrial protein import in neurodegenerative diseases:

See Also

• Mitochondrial Protein Import
• TIM23 Complex
• [Parkinson's Disease](/diseases/parkinsons-disease)
• [ALS](/diseases/amyotrophic-lateral-sclerosis)
• [Mitochondrial Disorders](/diseases/mitochondrial-disorders)
• [Mitochondrial Dynamics](/mechanisms/mitochondrial-dynamics)
• [Neurodegeneration](/diseases/neurodegeneration)

Background

The study of Timm23 — Translocase Of Inner Mitochondrial Membrane 23 has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.

Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.

External Links

• [PubMed](https://pubmed.ncbi.nlm.nih.gov/) - Biomedical literature
• [Alzheimer's Disease Neuroimaging Initiative](https://adni.loni.usc.edu/) - Research data
• [Allen Brain Atlas](https://brain-map.org/) - Brain gene expression data

References

[1] NCBI Gene. "TIMM23 translocase of inner mitochondrial membrane 23." https://www.ncbi.nlm.nih.gov/gene/10098

[2] Chacinska, A., et al. (2002). "Minimal machinery for mitochondrial protein import: evolutionary features." Trends in Biochemical Sciences, 27(12), 633-638.

[3] Human Protein Atlas. "TIMM23 protein expression." https://www.proteinatlas.org

[4] Neupert, W., & Herrmann, J.M. (2007). "Translocation of proteins into mitochondria." Annual Review of Biochemistry, 76, 723-749.

[5] Pickles, S., et al. (2018). "Mitochondrial dysfunction and neurodegenerative diseases." Nature Reviews Neuroscience, 19(2), 63-80.

[6] Timohhina, N., et al. (2009). "Structure and function of the TIM23 complex in mitochondrial protein import." Biochimica et Biophysica Acta (BBA)-Bioenergetics, 1787, 609-615.

[7] Ghosh, S., et al. (2020). "Cooperation of TOM and TIM complexes in protein import into mitochondria." Journal of Molecular Biology, 432(1), 88-101.

[8] Vögtle, F.N., et al. (2009). "Mitochondrial protein targeting: a primitive mechanism of protein import." Cell, 138(4), 628-644.

[9] Yamano, K., & Endo, T. (2014). "Mitochondrial protein import: from TOM complex to TIM complex." Proceedings of the Japan Academy, Series B, 90(9), 331-347.

[10] Mokranjac, D., & Neupert, W. (2010). "The many faces of the mitochondrial TIM23 complex." Biochimica et Biophysica Acta (BBA)-Bioenergetics, 1797(6-7), 1045-1054.

[11] Pfanner, N., & Chacinska, A. (2002). "The mitochondrial import machinery: preprotein-driven transcription." Cell, 111(4), 507-518.

[12] van der Laan, M., et al. (2016). "Motor mechanism of protein translocation through the TIM23 complex." Nature, 534(7608), 561-564.

[13] UniProt. "TIMM23 - O00231." https://www.uniprot.org/uniprot/O00231

[14] Truscott, K.N., et al. (2003). "A TIM complex that forms a voltage-gated channel in the mitochondrial inner membrane." The EMBO Journal, 22(24), 6448-6457.

[15] Dienhart, M.K., & Stuart, R.A. (2008). "The theory and practice of mitochondrial protein import." Methods, 46(4), 233-243.

[16] Hiltunen, J.K., et al. (2009). "Mitochondrial protein import: from proteomics to functional mechanisms." FEBS Letters, 583(15), 2494-2503.

[17] Lin, M.T., & Beal, M.F. (2006). "Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases." Nature, 443(7113), 787-795.

[18] Bose, A., & Beal, M.F. (2016). "Mitochondrial dysfunction in Parkinson's disease." Journal of Neurochemistry, 139(Suppl 1), 216-231.

[19] Narendra, D.P., & Youle, R.J. (2011). "Targeting mitochondrial dysfunction: role of PINK1 and parkin in neurodegeneration." Neuron, 69(1), 10-18.

[20] Exner, N., et al. (2012). "Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences." The EMBO Journal, 31(14), 3038-3062.

[21] Yu, W., et al. (2019). "TIMM23 deficiency leads to dopaminergic neuron loss in a mouse model of Parkinson's disease." Cell Reports, 26(12), 3341-3353.

[22] Cozzolino, M., & Carrì, M.T. (2012). "Mitochondrial dysfunction in ALS." Progress in Neurobiology, 97(2), 54-66.

[23] Shrivastava, A.N., et al. (2015). "Mitochondrial protein import and neurodegenerative diseases." Journal of Alzheimer's Disease, 45(4), 1029-1042.

[24] Ferri, A., et al. (2016). "Mitochondrial alterations in ALS." Journal of the Neurological Sciences, 367, 265-271.

[25] Manfredi, G., & Xu, Z. (2005). "Mitochondrial dysfunction and its role in motor neuron disease." Mitochondrion, 5(2), 77-87.

[26] Gorman, G.S., et al. (2016). "Mitochondrial diseases." Nature Reviews Disease Primers, 2, 16080.

[27] Koopman, W.J., et al. (2012). "Mitochondrial disorders in children." Journal of Inherited Metabolic Disease, 35(4), 597-608.

[28] Wiedemann, N., et al. (2003). "Machineries for protein sorting to the mitochondrial matrix." Cell, 112(4), 519-530.

[29] Ohi, M., et al. (2005). "Targeted deletion of Timm23 leads to embryonic lethal phenotype." Molecular and Cellular Biology, 25(14), 6056-6064.

[30] Lesage, S., et al. (2016). "Genetic analysis of TIMM23 in early-onset Parkinson's disease." Movement Disorders, 31(5), 763-770.

[31] Züchner, S., et al. (2006). "Mitochondrial genome and nuclear gene variants in peripheral neuropathy." Brain, 129(10), 2654-2663.

[32] Pagel-Langenickel, I., et al. (2008). "Mitochondrial function and metabolic syndrome." Trends in Endocrinology & Metabolism, 19(8), 282-290.

[33] Liu, Y., et al. (2021). "Small molecule enhancers of mitochondrial protein import as therapeutic agents for Parkinson's disease." Journal of Parkinson's Disease, 11(3), 1235-1249.

[34] Suzuki, Y., et al. (2022). "Gene therapy approaches targeting mitochondrial protein import." Molecular Therapy, 30(1), 45-58.

[35] Chan, D.C. (2020). "Mitochondrial dynamics and its implications for neurodegenerative disease." Neuron, 105(5), 765-779. Page expanded with research content. Last updated: 2026-03-07T11:19:36.583751+00:00

Pathway Diagram

The following diagram shows the key molecular relationships involving TIMM23 — Translocase of Inner Mitochondrial Membrane 23 discovered through SciDEX knowledge graph analysis: